Next Article in Journal
N-Methylcytisine Ameliorates Dextran-Sulfate-Sodium-Induced Colitis in Mice by Inhibiting the Inflammatory Response
Next Article in Special Issue
Melatonin and Cancer Hallmarks
Previous Article in Journal
Physicochemical Characterization and Functional Analysis of the Polysaccharide from the Edible Microalga Nostoc sphaeroides
Previous Article in Special Issue
Melatonin-Mediated Development of Ovine Cumulus Cells, Perhaps by Regulation of DNA Methylation
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:

Mitochondria: Central Organelles for Melatonin′s Antioxidant and Anti-Aging Actions

Department of Cellular and Structural Biology UT Health San Antonio, San Antonio, SD 78229, USA
Centro de Investigacion Biomedica de Occidente, Instituo Mexicana del Seguro Social, Guadalajara 44346, Mexico
Departamento de Quimica, Universidad Autonoma Metropolitana-Iztapatapa, Mexico D.F. 09340, Mexico
Author to whom correspondence should be addressed.
Molecules 2018, 23(2), 509;
Submission received: 9 January 2018 / Revised: 13 February 2018 / Accepted: 16 February 2018 / Published: 24 February 2018


Melatonin, along with its metabolites, have long been known to significantly reduce the oxidative stress burden of aging cells or cells exposed to toxins. Oxidative damage is a result of free radicals produced in cells, especially in mitochondria. When measured, melatonin, a potent antioxidant, was found to be in higher concentrations in mitochondria than in other organelles or subcellular locations. Recent evidence indicates that mitochondrial membranes possess transporters that aid in the rapid uptake of melatonin by these organelles against a gradient. Moreover, we predicted several years ago that, because of their origin from melatonin-producing bacteria, mitochondria likely also synthesize melatonin. Data accumulated within the last year supports this prediction. A high content of melatonin in mitochondria would be fortuitous, since these organelles produce an abundance of free radicals. Thus, melatonin is optimally positioned to scavenge the radicals and reduce the degree of oxidative damage. In light of the “free radical theory of aging”, including all of its iterations, high melatonin levels in mitochondria would be expected to protect against age-related organismal decline. Also, there are many age-associated diseases that have, as a contributing factor, free radical damage. These multiple diseases may likely be deferred in their onset or progression if mitochondrial levels of melatonin can be maintained into advanced age.

1. Introduction

A surplus of chemically-reduced oxygen derivatives, often referred to as reactive oxygen species (ROS), some of which are free radicals (with an unpaired valence electron), commonly leads to an augmented level of molecular damage identified as oxidative stress [1]. The excess of highly reactive oxygen metabolites overwhelms a complex antioxidant defense network such that it does not adequately defend against the consequent deleterious effects. All major molecular groups typically sustain damage when attacked by free radicals, but the level of oxidative stress is most frequently based on the quantities of damaged lipid products, protein carbonyls, and mutilated nucleic acids [2]. While many of the toxic derivatives of ground state oxygen are oxygen-based and therefore are referred to as reactive oxygen species (ROS), others are nitrogen (RNS) or chlorine (RCS)-based. For the purposes of the current report, these are all considered under the collective term of ROS. Likewise, the damage inflicted by ROS, depending on the species involved, is referred to as either oxidative stress or nitrosative stress. Herein, both are categorized as oxidative stress.
The generation of ROS, including free radicals, is inevitable and continuous in aerobic organisms [3]. Since their creation cannot be totally smothered, the alternative is to neutralize them before they vandalize a neighboring critical molecule. This is obviously not a foolproof task for cells, however, since invariably some radicals escape incapacitation and destroy bystander molecules, thereby compromising organellar physiology. Less than optimal functioning of subcellular systems can undermine cellular metabolism leading to physiological inefficiency and, in the worst case scenario, cell death [4].
To make matters worse, once formed, free radicals can cause a chain reaction of events that leads to massive molecular annihilation of healthy structures. This occurs when the first free radical formed extracts an electron from an otherwise normal molecule in its vicinity, causing it to become a destabilized free radical; in turn, it captures an electron from another molecule to sabotage it. This domino process is especially well defined in reference to lipid peroxidation and is only interrupted when an antioxidant intervenes and scavenges the perpetuating free radical or an intermediate toxic derivative [5].
Not all free radicals are pariahs. While under conditions of oxidative stress in non-pathological cells, they produce an imbalance between the reductive power of the cell and the oxidation state in favor of the latter, under some conditions, they serve as beneficial signaling molecules [6,7]. Undoubtedly, ROS have several characteristics typical of second messengers, including their short half-life, as well as the ability to amplify a series of reactions that are initiated by a primary ligand. In particular, O2 and H2O2 can function as intracellular signaling molecules; this is assisted, especially in the case of H2O2, by its ability to readily pass through cellular membranes. The production of the superoxide anion radical (O2) and hydrogen peroxide (H2O2) are carefully regulated intracellularly [8,9]. This, however, does not apply to the hydroxyl radical (•OH). Finally, ROS and free radicals are sometimes produced in abundance in cancer tissues that aid in the killing of these disease-causing cells [9]. A notable conundrum that becomes apparent when considering the differential actions of ROS and free radicals is how antioxidants/free radical scavengers discriminate between those that are potentially harmful while mostly sparing those mediating beneficial signal transduction processes [10]. Even when very large amounts of an antioxidant are given, the signaling pathways that utilize ROS seem to be left functionally intact.

2. Melatonin Origin and Distribution

While there are many molecules that potentially function as free radical scavengers, in the current survey, we only summarize the actions and mechanisms of melatonin and its metabolites in terms of their ability to forestall the cellular damage associated with an excess of ROS. Because of its presence in bacteria [11,12], which evolved several billion years ago, we have speculated that melatonin is phylogenetically the oldest antioxidant in existence [13]. Considering its longevity, throughout evolution melatonin has had ample opportunity to hone and diversify its functions in its quest to vanquish toxic oxygen derivatives [14,15], as well as to inherit other functions [16,17,18]. In addition to its presence in all taxa of the animal kingdom (where attempts to measure it have been made), its discovery in land plants [19,20], along with its verification and functional definition in many plant species [19,20,21,22], suggests there is no organism on Earth that lacks this important molecule. Melatonin (and its metabolites) in plants have many of the same functions as this indole has in animals [23,24,25,26].
It has been argued that because of its seemingly lower concentration intracellularly relative to other well-documented antioxidants, e.g., glutathione in neurons and hepatocytes, melatonin would not successfully compete as a free radical scavenger, e.g., of the •OH, which has an extremely short half-life and creates damage only in the immediate vicinity of where it is generated [27]. For any radical scavenger to neutralize the •OH, it is essential that it be at the immediate vicinity of the toxic species. Thus, the total concentration of an antioxidant within a cell may be less important than its concentration at the site of free radical generation. Recently, it was demonstrated that melatonin is in especially high concentrations in mitochondria, an organelle in which free radicals are produced in abundance [28,29]. At least relative to this organelle, melatonin may be “in the right place all of the time” to resist oxidative stress. Thus, melatonin may have a positional advantage that other antioxidants do not share that improves its ability to scavenge toxic radicals and reduce the associated oxidative stress [30]. Judging from its very different concentrations in the bodily fluids of organisms, e.g., blood versus cerebrospinal fluid (CSF) [31], versus ovarian follicular fluid [32], versus bile [33], etc., this may speak to a positional advantage melatonin may have in terms of protecting against oxidative stress. Undoubtedly, any judgement about the levels of melatonin throughout an organism based solely on its concentrations in the blood is erroneous [30].
The specific concentrations of melatonin in a given bodily fluid varies widely depending on a number of factors, e.g., time of day of fluid collection (blood and cerebrospinal fluid (CSF), levels are much higher at night than during the day [31,34]) and the site of fluid collection (melatonin concentrations measured in blood obtained from the vascular sinus surrounding the pineal gland differ from levels in peripherally-collected blood [35,36]); for cerebrospinal fluid (CSF), melatonin levels are higher in this fluid collected from the third ventricle when compared to values in CSF collected via lumbar puncture [31,37]. In reference to ovarian follicles, the fluid of small vesicular follicles has lower melatonin levels than the fluid obtained from large follicles [38]. Moreover, circulating concentrations of melatonin may vary depending on food recently consumed [39], level of stress [40], quality of light exposure [41], age [42], reproductive state [43], use of drugs (medications) [35], presence or absence of disease [44], opacity of the lens in the eye [45], etc.
Melatonin also works via multiple means to limit oxidative stress. While melatonin is capable of directly or indirectly scavenging toxic oxygen species [46,47,48], it has other means at its disposal for combatting free radical damage. When a molecule such as melatonin merely renders one of its delocalized electrons to neutralize a free radical, this action is achieved without receptor intervention [47,49]. It is well documented, however, that melatonin’s ability to limit oxidative stress sometimes also relies on its interaction with melatonin membrane receptors that are present in many, perhaps all, cells [50,51]. These antioxidant actions of melatonin rely on an interaction with membrane receptors located on the cell membrane or on intracellular organelles [52,53,54]; membrane receptors for melatonin also may exist in all organisms [30]. These receptor-mediated actions of melatonin are indirect and likely involve stimulation of antioxidant enzymes, e.g., glutathione peroxidase (GPx), superoxide dismutase (SOD1, 2), SIRT3, etc. [55,56]. When melatonin acts via receptors to carry out its antioxidant actions, it can achieve this effect at much lower concentrations than those required when it functions as a direct free radical scavenger. This relates to the fact that the signal transduction pathways associated with receptors serve to magnify the response. A final feature that characterizes melatonin as an important antioxidant is its availability from multiple sites. Vitamins C and E are only available to humans when they are consumed in the diet. In contrast, given its widespread presence in edible plants [21,26], melatonin is obtained from the food consumed and, furthermore, it is produced in all organisms, perhaps in every cell that has mitochondria or chloroplasts [57,58,59]. As with animals, the concentrations of melatonin in plants vary widely and depend on the plant organ in which melatonin is measured [20,21,60], the physiological state of the plant [26], etc.
Historically, melatonin was thought to be uniquely of pineal gland origin [61,62]. It is now clear that this is not the case, since only vertebrates have a pineal gland, while other animal species and plants lack even a homologous organ. In vertebrates, the circadian synthesis and secretion of melatonin, particularly into the CSF, has a two-fold function; the melatonin rhythm in the CSF is for the purpose of circadian rhythm regulation at the level of the suprachiasmatic nucleus (SCN) and perhaps to protect the brain from oxidative stress [63,64]. However, the pineal gland is not a requirement for the circadian production of melatonin. In the microalga, Gonyaulax polyhedra (also known as Lingulodinium polyedrum), there is a distinct light:dark-driven melatonin cycle similar to that in vertebrates, but this is a single cell species that obviously has no organs [65].

3. Sites of Reactive Oxygen Species Generation

Mitochondria are a major site for the generation of ROS including free radicals. ROS species, as mentioned in the Introduction, may or may not be damaging to cellular constituents. The oxygen-derived species that have generally low reactivity, e.g., the product of the single reduction of ground state oxygen, the superoxide anion radical (O2), and its enzymatic product hydrogen peroxide (H2O2) can sometimes serve as second messengers within cells [7,66] while also being precursors of more reactive and destructive species, e.g., the hydroxyl radical (•OH) and peroxynitrite (ONOO), a non-radical but highly oxidizing species (Figure 1). Furthermore, ONOO may degrade into the •OH [67].
The molecular damage inflicted by especially highly-reactive ROS can be controlled by either preventing the formation of their precursors, i.e., the weakly reactive ROS, or by scavenging them as soon as they are produced. Melatonin has both these capabilities; it reduces O2 formation at the level of the mitochondrial electron transport chain (ETC) by a process referred to as radical avoidance [68], and it is a direct ROS scavenger [15,30,69,70,71] (Figure 1). In addition, melatonin lowers the ROS burden by promoting enzymes that metabolize low reactive ROS to oxygen and water. These enzymes include the superoxide dismutases (SOD1, SOD2), which remove O2, the glutathione peroxidases (GPx), and the peroxiredoxins (PRs), which rids the cellular microenvironment of H2O2. There are no enzymes that metabolize the most toxic ROS varieties, i.e., •OH and ONOO, to innocuous molecules. While SOD, GPx, and PRs are all known to be regulated by melatonin, the data related to SOD and GPx [72,73,74] is more extensive than that for PRs [75,76].
The mechanisms by which melatonin or its metabolites modulate antioxidant enzyme activities have not been unequivocally identified. Some proposed mechanisms include their ability to inhibit the ubiquitination of Nrf2, thereby allowing it to translocate to the nucleus and bind to the antioxidant response element (ARE), which leads to the activation of the associated enzymes [15,77,78]. Melatonin may also modulate SIRT3/SOD2 signaling in the mitochondria to regulate the degree of oxidative stress in this organelle [58].
Within mitochondria, there are numerous sites at which ROS could potentially be generated [79]. The sites that have the greatest potential of doing so under in vivo conditions involve the electron transport chain (ETC). Thus, respiratory Complex I (NADPH: ubiquinone oxidoreductase) and Complex III (ubiquinol: cytochrome c reductase) leak electrons when they are shunted between donor and receptor molecules [80] (Figure 2). The ROS generated by Complex I appear in the matrix, while those from Complex III are divided between the matrix and intermembrane space [81]. Again, while the ROS produced in mitochondria sometimes have physiological relevance [82], their production in excess, as occurs during aging [83,84] and many other pathologies [85,86,87,88,89], has dire consequences due to the damage they inflict.
While the mitochondrial source of ROS is considered of high significance in terms of disease processes and aging-related cellular and organismal decline, intracellular enzymes outside the mitochondria are also a source of ROS. Some of the major enzymes in this group include monoamine oxidase (MAO), peroxisomal enzymes, NADPH oxidases (NOX), and xanthine oxidase (XO) [76]. NOX, a family of cytosolic enzymes, are of particular importance in terms of producing O2 and H2O2 [90]. These agents can give rise to the •OH via the Fenton reaction and, therefore, NOX enzymes also have been implicated in disease states [91]. XO and MAO are bound to the outer mitochondrial membrane and are free in the cytosol [92,93]. Their generation of ROS increases with age and MAO activity; in particular, it contributes to a major neurodegenerative disease in the aged, i.e., Parkinson disease, in which the dopaminergic neurons of the pars compacta are destroyed [94,95].
The cytosolic peroxisome plays a major role in not only the production of H2O2 but also its detoxification [96]. Disturbances in the redox balance in this organelle promote cellular senescence due to elevated H2O2 [97]. Additionally, lysosomes release free metal ions such as iron which, via the Fenton reaction, promote •OH formation that advances oxidative stress [98].
While ROS are produced in many portions of every cell, the current review is mainly concerned with mitochondrial ROS (mtROS) and how melatonin functions to combat their toxicity. As will be further elaborated in a later section of this report, melatonin is in especially high concentrations in mitochondria [28], likely due to its rapid uptake [99] and synthesis in this organelle [100,101,102]. The indole is also present in other subcellar compartments but in lower concentrations than in the mitochondria [28].
The subcellular distribution of melatonin has been sparingly investigated. Thus, while the differential concentrations of melatonin in various subcellular compartments have been described in a number of cells in different organs [28,103], many cell types have yet to be examined in this regard. Nevertheless, there are numerous reports that support melatonin′s ability to protect molecules in the inner mitochondrial membrane from the toxicity of ROS [104,105,106]. Since the very high reactivity and extremely short half-life of some ROS, e.g., •OH, preclude its transport from where it is produced, if melatonin is to counteract its action in mitochondria, melatonin must be in the immediate vicinity of where the •OH is generated [107,108,109,110,111,112].

4. Melatonin and Its Metabolites: Determinants of Oxidative Stress

That melatonin is highly effective in reducing oxidative damage is illustrated in an extensive list of reports published in the last 25 years [113,114,115,116,117]. Mechanistically, the means by which melatonin neutralizes ROS is also well described and includes direct scavenging actions [30,47,118,119,120,121] and indirect processes by which ROS is enzymatically converted to less harmful species [14,107,122,123,124]. In mitochondria, the enzymatic dismutation of O2 involves the stimulation of SIRT3 by melatonin; this leads to the deacetylation and activation of SOD2, thereby limiting oxidative damage to this vital organelle [125,126,127]. The action of melatonin at the mitochondrial level is consistent with its designation as a mitochondria-targeted antioxidant [14,71].
While melatonin very effectively reduces oxidative stress in all experimental and clinical settings in which it has been tested [87,128,129,130,131], it has an advantage over other antioxidants, since not only is melatonin a scavenger of toxic species, but several of its products are as well [132,133] (Figure 3). In what is referred to as melatonin's antioxidant cascade, after melatonin interacts with a toxic species it is metabolized enzymatically or non-enzymatically to other antioxidants that are equal to or better than melatonin in detoxifying free radicals [134]. These metabolites include cyclic 3-hydroxymelatonin [135], N1-acetyl-N2-formyl-5-methoxykynuramine (AFMK) [132], N1-acetyl-5-methoxykynuramine (AMK) [133], and perhaps others. Thus, whereas classical antioxidants scavenge a single radical, via its cascade of reactions, melatonin detoxifies multiple radical species. This, coupled with its indirect antioxidant actions described above and its ability to bind transition metals [136], causes melatonin to be a potent repressor of oxidative stress. Moreover, a variety of melatonin analogues, which are produced in vivo, also function as antioxidants [137]. Finally, after being damaged by free radicals, melatonin aids in promoting DNA repair [138].
Considering the wide array of complex actions that melatonin seemingly manifests relative to reducing oxidative stress, it is likely that our understanding of how melatonin actually functions in a highly oxidizing environment is wholly incomplete. The mechanisms that have been put forth to explain melatonin′s comprehensive capacity to provide antioxidant protection leads one to surmise that what is being observed are merely epiphenomena of a more basic molecular action of this phylogenetically-ancient molecule. Future research will likely reveal additional actions(s) of this functionally-diverse agent.

5. Melatonin in Mitochondria: A Fortuitous Association

A recently published issue of Cellular and Molecular Life Sciences (Volume 74, Issue 21, 2017) is solely devoted to describing the multiple actions of melatonin at the mitochondrial level. These actions likely necessitate that melatonin is present in this organelle. In early immunocytochemical studies, we documented that when astrocytes are challenged in vitro with H2O2, their mitochondria exhibit an enhanced free radical fluorescence [139]; this enhancement is markedly blunted if, in addition to H2O2, the cells are simultaneously incubated with melatonin; this protection was superior to that provided by vitamin E. Likewise, using multiple fluorescence imaging microscopy, we observed that melatonin also protects mitochondria from elevated mitochondrial Ca2+ (mCa2+) stress [140,141]. Thus, melatonin completely attenuated mROS induced by mCa2+ due to exposure to ionomycin. Also, melatonin prevented mCa2+-mediated mitochondrial permeability transition (MPT), indicating that melatonin may directly target the MPT. When astrocytes were treated with cyclosporine A, a MPT inhibitor, melatonin reduced Ca2+-induced cellular apoptosis, showing that melatonin also had actions beyond the MPT.
Many studies during the last two decades have further defined the critical role that melatonin has in maintaining the optimal physiology of the mitochondria [14,30,87,106,115,142,143,144]. The beneficial actions of melatonin at the level of the mitochondria are apparent in reference to quenching free radicals, reducing oxidative stress, limiting mitochondria-related apoptosis, maintaining the efficiency of the respiratory chain complexes, and ensuring ample ATP production [145,146,147]. Moreover, these regulatory actions are not unique to a single cell type but rather are applicable to every cell, plant, and animal that has mitochondria.
The remarkable ability of melatonin to preserve mitochondrial function implies that it gets into this organelle in sufficiently high concentrations to protect them from dysfunction under the most extreme oxidizing conditions. There is, however, limited information on the levels of melatonin in subcellular compartments. The one study that made such measurements indicates that, at least in brain cells, melatonin concentrations in mitochondria far exceed those in the blood [28]. While higher than blood levels were also estimated in hepatocyte mitochondria, they were significantly lower than in brain cells. This great difference between these tissues could relate to the much higher concentrations of melatonin in the cerebrospinal fluid (CSF) [148,149], to which brain cells are exposed [150], relative to the much lower levels of melatonin in the blood, to which hepatocytes are exposed. Alternatively, it could relate to the high metabolic demands of neurons versus liver cells. Studies related to the immunocytochemical localization of melatonin at the subcellular level certainly suggest that melatonin quickly enters cells and has ready access to mitochondria [139,140]. The evidence related to the mechanisms by which melatonin may pass through cell membranes was recently reviewed by Mayo and coworkers [151].
Since melatonin is highly lipid soluble, it has often been assumed that it enters cells by simple diffusion. Under detailed examination, however, its passage through the plasma membrane seemed to be dependent on the presence of a protein that was identified as a glucose transporter, GLUT 1 [152]. Docking studies also prompted the conclusion that melatonin′s entrance into the cell was related to the GLUT 1 transporter. This process was slower than expected, however, and did not provide information on how it may contribute to levels of melatonin in mitochondria.
The most complete description of the means by which melatonin enters mitochondria against a gradient is provided by the recent study of Huo et al. [99]. Using two human cancer cell lines (PC3 and U118), this group tested whether either the organic ion transporter, OAT3, or the oligopeptide transporters, PEPT1/2, facilitated melatonin′s transfer through the mitochondrial membranes. The study revealed that the OAT3 transporter was not related to melatonin’s movement into the mitochondria. On the contrary, however, melatonin transport into this organelle was facilitated by PEPT1/2. Docking analysis studies showed that the ability of melatonin to bind to PEPT1/2 related to their low binding energy and optimal binding configuration given that melatonin readily embedded in the active site of the transporters and nestled in the cavity in three dimensional space [99]. Melatonin uptake through PEPT1/2 was linear and its uptake was saturable during prolonged incubation. When Bes, a competitor for the receptors, was added to the incubation medium, melatonin uptake was significantly reduced. The optimal pH for the movement of melatonin through the transporter was 5.5; this is the pH at which PEPT1/2 function maximally. Finally, knockdown of PEPT1/2 expression with siRNAs showed that the amount of melatonin in mitochondria was related to the presence of PEPT1/2 in the membranes of this organelle (Figure 4). Despite the completeness of these studies, the authors left open the possibility that simple diffusion or other yet-to-be-identified transporters may also be involved in the movement of melatonin from the cytosol into the mitochondria. While the findings of Huo et al. [99] are highly significant, whether they will be applicable to other cell types and, in particular, to normal cells (they used cancer cells exclusively) certainly warrants investigation.
In agreement with the observations showing the importance of oligopeptide transporters in hastening the movement of melatonin into mitochondria are studies that compared melatonin with Mito E and Mito Q in terms of their ability to protect cells under extremely high oxidative stress conditions [153]. Mito E and Mito Q are synthetic antioxidants that accumulate in mitochondria at levels up to 500-fold greater than the unaltered antioxidants, i.e., vitamin E and co-enzyme Q10. When rats were treated with two bacterial toxins, lipopolysaccharide (LPS) and peptidoglycan (PepG), which cause severe acute sepsis, there was evidence of substantial malfunction of two organs in which it was assessed, i.e., liver and kidney [153]. In an attempt to protect the organs from damage, the toxin-treated rats were intravenously infused with equimolar concentrations of either Mito E, Mito Q, or melatonin. These molecules had broadly similar protective actions in terms of lowering oxidative stress, preserving mitochondrial respiration, depressing circulating interleukin-6 levels, and protecting against organ dysfunction, as indicated by blood levels of alanine aminotransferase (liver) and creatinine (kidney). In some cases, although it was not proven statistically, melatonin appeared superior to the synthetic molecules, Mito E and Mito Q. The ability of melatonin to protect against experimental [87,154,155] and clinical [156] sepsis is well documented. On the basis of their findings, Lowes and colleagues [153] proposed the use of melatonin over Mito E or Mito Q in clinical trials designed to attenuate mitochondrial oxidative stress and cellular dysfunction. Considering that Mito E and Mito Q concentrate in the mitochondria up to 500 times greater than the levels in the blood, along with the fact that melatonin provides equal or better protection, it can be assumed that the indole was also in high concentrations in mitochondria.
Given what is known about the seemingly high levels of melatonin in mitochondria and the ability of this compartment to avidly take up the indole, the speculation that melatonin is targeted to the mitochondria is certainly justified [30,57,71,157]. Elevated mitochondrial melatonin levels would certainly be advantageous, since these organelles produce the bulk of the damaging free radicals that most cells generate. Moreover, since they are the site of origin of the majority of the ATP, they are absolutely vital to the survival of a cell. This being the case, it should not be unexpected that mitochondria would have access to a highly potent antioxidant, such as melatonin.
The detection of melatonin in the earliest-evolved organisms, i.e., bacteria [11,12,158], along with theory that mitochondria/chloroplasts evolved from bacteria that were initially ingested by prokaryotes as food [159] (Figure 5), prompted the speculation that mitochondria/chloroplasts retained the melatonin-forming ability of their bacterial precursors [100]. This would be a very fortuitous arrangement given the fact that, as already mentioned herein, mitochondria have a propensity to produce an abundance of free radicals as a byproduct of oxidative phosphorylation [57,71,142,157]. Recently published data supports the high likelihood that both mitochondria [71,100,101,102,160] and chloroplasts [161,162] are in fact sites of melatonin synthesis.
In reference to melatonin synthesis by mitochondria, He and colleagues [160] isolated these organelles from mouse oocytes and showed, immunocytochemically, that they express the rate limiting enzyme in melatonin synthesis, serotonin N-acetyltransferase. When purified mitochondria were incubated with serotonin for 1 hour, the melatonin concentration in the culture medium rose dramatically. Since mitochondria were the only organelles in the incubation medium, it was assumed the rise in melatonin in this fluid was a consequence of its sustained production by mitochondria. As physiological evidence that melatonin was present in mitochondria, the amount of melatonin correlated with several parameters that were improved in these organelles (increased mtDNA copies, elevated ATP, enhanced mitochondrial membrane potential, etc.).
The most complete documentation of mitochondria being the site of melatonin synthesis comes from a recent study of Suofa et al. [102]. They reasoned that since melatonin levels are highly elevated in brain mitochondria [28], that it may also be produced in these organelles. With this rationale and using rat forebrain non-synaptosomal mitochondria, they tested whether the melatonin-forming enzymes, i.e., arylalkylamine N-acetyltransferase (AANAT) and N-acetylserotonin-O-methyltransferase (ASMT), are also present. When these constituents were measured, the authors found this to be the case. Additionally, 14-3-3 was also located in the mitochondria (and in the cytosol); 14-3-3 is a chaperone that is present in the pineal gland [62] and protects AANAT from degradation and improves its affinity for serotonin, the substrate for the enzyme [163]. Digestion of the outer mitochondrial membrane with a combination of proteinase K and digitonin (which left the inner mitochondrial membrane intact) revealed that the remaining mitochondrial fraction retained the AANAT and ASMT activities, suggesting their location in the mitochondria matrix. Unlike in the pineal gland, mitochondrial AANAT activity did not vary over a light:dark cycle. When AANAT was knocked out in mouse neuroblastoma cells (N2a), mitochondria exhibited a much higher degree of oxidative stress in response to oxygen/glucose deprivation; this is consistent with the absence of melatonin, since it is a potent inhibitor of oxidative damage [71]. Finally, when purified mouse forebrain mitochondria were incubated with deuterated (D4) serotonin along with ATP and respiratory substrate, they quickly formed D4-N-acetylserotonin and D4-melatonin.
The importance of the findings suggesting that mitochondria produce their own melatonin cannot be over emphasized. Mitochondria are a major site of free radical generation and, therefore, oxidative damage. Malfunctions of mitochondria have numerous debilitating consequences in terms of cellular loss, organ dysfunction, and organismal decline (see below).
In view of the data reported, we predict that melatonin will be inducible in mitochondria as has been shown in plants [21,26,164,165,166]. We suspect the stimulus for the compensatory rise in mitochondrial melatonin production will be the quantity of free radicals being formed in these organelles or the amount of oxidative damage being sustained. When the dinoflagellate Lingulodinium polyedrum (nee, Gonyaulax polyhedron) is exposed to a reduced ambient temperature, a situation that augments free radical generation in these unicells, melatonin levels in these organisms rise dramatically [167]. The increase is likely related to the de novo synthesis of the indole. As noted above, a compensatory elevation in melatonin levels is also a common feature of land plants when they experience any of a number of stresses [21,26,164,165,166].

6. Melatonin, Oxidative Stress, and Aging

That morphological, functional, and molecular deterioration occurs with increasing age is indisputable for all living organisms; however, the rate at which different taxa degenerate varies widely. A reliable explanation for these differences is yet to be fully defined and, in fact, aging mechanisms of a given species likewise constitute a major point of scientific debate.
The subcellular organelle most frequently implicated in terms of determining the rate of aging is the mitochondrion [168,169]. Moreover, it is the elevated free radicals that they produce that theoretically help to explain their age-related dysfunction. The free radical theory of aging has persisted for more than 50 years [170,171], but the evidence supporting it is still not beyond dispute [165,168].
Since free radicals obviously cause molecular disfigurement and functional decay, and given that they are abundantly created in mitochondria, molecules that either efficiently quench a variety of ROS species or reduce their production, especially in mitochondria, may be useful as a means to slow the rate of aging and reduce age-related diseases [172,173]. To enhance their entry into mitochondria, industry has synthesized synthetic antioxidants [174,175] that do accumulate up to 500-fold (greater than the natural antioxidant) in the mitochondrial matrix. Despite this, these modified radical scavengers are no better than melatonin in fending off ROS-mediated damage [138]. Because of this and for other reasons, interest is the role of melatonin in aging processes has been a topic of interest for more than two decades [176,177,178].
In 1999, we [179] reported that surgical removal of the pineal gland from young rats caused a more rapid accumulation of oxidatively-damaged molecules in multiple tissues when the animals reached 25 months of age. Pinealectomy deprives animals of melatonin that are normally secreted by the pineal, but not from other organs. Thus, the animals were not devoid of melatonin but they presumably were relatively melatonin deficient compared to pineal-intact animals. The findings could mean that the partial loss of the antioxidant, melatonin, was responsible for the accelerated oxidative damage measured later in life, i.e., the animals aged more rapidly. The data, however, must be considered in light of another action of melatonin not related to its free radical scavenging actions. Since the circadian rhythm of melatonin feeds back onto the master biological clock, SCN, to aid in the synchronization of rhythms throughout the organism [180], the circadian disruption due to pineal removal may have led to the excessive accumulation of oxidative damage [181,182]. The loss of the endogenous melatonin rhythm is always accompanied by some total body circadian dysregulation [183]. Twenty-four hour rhythms are also fundamental properties of mitochondria with both their morphology and physiology being periodic [184]. Systematic, as well as intrinsic, cues probably drive these mitochondrial cycles [87]. Thus, when examining the actions of melatonin on molecular aspects of aging, and diseases associated with advancing age, it is important to note that melatonin may have positive actions beyond its ability to squelch oxidative stress, i.e., function as an antioxidant. The multiple actions of melatonin may explain why melatonin is better than conventional antioxidants in preserving optimal cell physiology and seemingly improving health.
Considering the multiple critical functions of mitochondria, it is not unexpected that they would be the focus of research related to aging. The diverse functions of this organelle include optimizing oxidative phosphorylation (OXPHOS), which culminates in ATP production; during this process oxygen-based radical and non-radical products are formed that, in the long term, damage the mitochondria. This organelle also participates in metabolic and signaling pathways including the regulation of apoptosis. The mitochondria also possess their own genetic material [mitochondrial (mt)DNA]. mtDNA encodes some of the proteins that are components of the respiratory complexes. Given the inadvertent production of ROS during OXPHOS, mtDNA is readily damaged, leaving it to form proteins of the respiratory chain that are flawed; when this occurs, the complexes become inefficient and produce higher numbers of damaging free radicals. These processes then become a progressively increasing cycle of destructive reactions leading to accelerated deterioration of mitochondrial physiology, which contributes to the aging phenotype [185,186].
Presumably, both because of their ability to uptake [99], as well as to synthesize [102], melatonin, the mitochondria contain sufficiently high concentrations of the indole to resist the mitochondrial melee initiated by ROS. There are numerous experimental data documenting melatonin’s ability to defer mitochondrial mutilation and dysfunction resulting from the excessive production of ROS due to the inefficient transfer of electrons between the respiratory complexes [84,125,128,130,144,153,187,188,189,190,191,192]. Melatonin likely achieves its protective effects because of its scavenging activities, as well as those of its metabolites [14,15,30,46,47,68,71], in addition to its indirect actions in the activation of mitochondria-located SOD2; in this case, melatonin stimulates SIRT3 activity, which prompts the deacetylation and activation of SOD2, thereby reducing the oxidative burden of the mitochondria [126].
Pineal-derived blood (and likely CSF) melatonin concentrations often wane as individuals age, thereby reducing the ability of melatonin to stabilize circadian rhythms and lowering its radical quenching ability [179,193]. Blood concentrations of melatonin diminish since its source, the pineal, loses its ability to synthesize it [194,195]. Hence, the drop-in melatonin is one of perhaps a number of factors that contributed to elevated oxidative injury in the elderly, including an increased incidence of diseases that have a significant free radicals component (Figure 6).
While it has been assumed that peripheral organ melatonin levels also drop with age due to a reduced local production, the evidence for this is scanty [196]. Nevertheless, we surmise that the total melatonin load is significantly greater in young animals (including humans) compared to old members of the species, and that the levels drop at a rather consistent rate in all organs as individuals age. The persistent shrinking levels of melatonin throughout life presumably contribute to the slow decline of organ function characteristic of aging. Certainly, the published literature is saturated with studies showing that restoring the diminished melatonin levels by supplementing them delays or restores physiological degeneration in old animals [84,85,87,95,104,197,198,199,200,201] and humans [88,202,203,204,205,206].
Paradies and colleagues [104] recently reviewed the expansive literature related to the degeneration of mitochondrial physiology during aging along with the capacity of melatonin to revitalize the function of these critically-important organelles. A reduction in the functional efficiency of the mitochondrial electron transport chain, including a diminished ability to generate ATP, has been repeatedly documented [142,145,207,208,209]. As discussed in their review, melatonin′s confirmed beneficial actions during aging very likely stem, in a major way, from its ROS scavenging activity in the mitochondrial matrix and intermembrane space [71]. In doing so, melatonin reduces oxidative damage, cardiolipin oxidation, MPTP opening, cytochrome c release, and cellular apoptosis. Melatonin may also have a direct action on the MPTP to reduce pore opening [210]. There is essentially universal agreement that shielding mitochondria from age-associated dysfunction would slow the processes of aging generally and especially the development of certain age-related diseases, e.g., neurodegenerative conditions [178,183,187,192,201,202]. Considering these data, melatonin′s multiple beneficial actions at the mitochondrial level seem to justify the conclusion that this endogenously-produced and exogenously-acquired indoleamine has a role in determining the rate at which both plants [211,212] and animals [178] age.

7. Concluding Remarks

Based on the literature surveyed in this review, it might be assumed that the routine long term use of supplemental antioxidants would aid in deferring aging and in delaying the onset or progression of age-associated diseases. However, taking conventional antioxidants, e.g., vitamins C or E, even in large quantities to improve performance or delay fragility has certainly not been unequivocally successful [213,214]. In contrast, the most frequent recommendation to support the anti-aging goals is dietary intake rich in multiple antioxidants and other nutrients [215].
Considering these observations and recommendations, it is reasonable to question whether treatment with melatonin, a molecule with obvious antioxidant activities, would yield results different than those provided (or not provided) by the vitamin antioxidants. When it functions to reduce oxidative damage, it is a more general antioxidant and displays multiple means to limit free radical damage [15,30,47,71,120,121]; this is a feature generally not shared by the vitamin antioxidants that have specific actions. Moreover, melatonin targeting to and synthesis in mitochondria likely affords it protective means not shared by the vitamin antioxidants. Thus, melatonin is an unconventional antioxidant with uncommon actions, some of which are probably yet to be identified.
It may also be futile to expect that the use of a single molecule would defer aging considering the complexity of the aging process [216]. Yet, interest in sole treatments such as metformin [217,218] is in vogue, and this molecule has generated a clinical trial [219]. Only two reports known to the current authors that compared the benefits of metformin relative to those of melatonin have been published [220]. In the first of these reports, the ability of melatonin and metformin, alone or in combination, to reduce testicular damage due to torsion-mediated ischemic injury was compared [221]. Histologically, these agents were equally effective in preserving spermatogenic activity and providing antioxidant protection to the gonads. Combining the two treatments, however, did not further improve the parameters measured in the ischemic testes. In the second report, melatonin and metformin were compared relative to their ability to limit oxidative stress to the heart of rats with mammary tumors [220]. Each molecule individually reduced free radical-mediated lipid and protein damage while promoting antioxidant enzyme activities, although melatonin was generally more effective in protecting against oxidative stress. The outcome of the latter comparison prompted the authors to conclude that melatonin has significantly greater antioxidant activity than metformin at the level of the heart. Experimental treatments that include both melatonin and metformin may be timely and could yield useful data for the design of clinical studies with an interest in modifying aging processes.
An important take-home message from this review is that melatonin should not be thought of as a regular antioxidant; the published data, which is extensive, indicates otherwise. The mere fact that it is both consumed in the diet and exogenously produced, perhaps in every mitochondria/chloroplast-containing cell of every living organism, makes melatonin unique. Additionally, the fact that melatonin is so closely associated with mitochondria should make it of significant interest in any study in which the endpoints include deferring the onset of diseases, improving the quality of life, or prolonging longevity.


No funding was provided in support of the research in this research summarized in this report.

Conflicts of Interest

None of the authors have a conflict of interest.


  1. Halliwell, B. Biochemistry of Oxidative Stress. Biochem. Soc. Trans. 2007, 35, 1147–1150. [Google Scholar] [CrossRef] [PubMed]
  2. Dasuri, K.; Zhang, L.; Keller, J.N. Oxidative Stress, Neurodegeneration and the Balance of Protein Degradation of Protein Synthesis. Free Radic. Biol. Med. 2013, 62, 170–185. [Google Scholar] [CrossRef] [PubMed]
  3. Halliwell, B. Reactive Oxygen Species in Living Systems: Source, Biochemistry and Role in Human Disease. Am. J. Med. 1991, 91, 145–225. [Google Scholar] [CrossRef]
  4. Yang, M.L.; Doyle, H.; Clarke, S.G.; Herold, K.; Mamula, M. Oxidative Modification in Tissue Pathology and Autoimmune Diseases. Antioxid. Redox. Signal. 2017, in press. [Google Scholar] [CrossRef] [PubMed]
  5. Agmon, E.; Stockwell, B.R. Lipid Homeostasis and Regulated Cell Death. Curr. Opin. Chem. Biol. 2017, 39, 83–89. [Google Scholar] [CrossRef] [PubMed]
  6. Ray, P.D.; Huang, B.W.; Tsaji, Y. Reactive Oxygen Species (ROS) Homeostasis and Redox Regulation in Cellular Signalling. Cell. Signal. 2012, 24, 981–990. [Google Scholar] [CrossRef] [PubMed]
  7. Weidings, A.; Kozlov, A.V. Biological Activities of Reactive Oxygen and Reactive Nitrogen Species: Oxidative Stress versus Signal Transduction. Biomolecules 2015, 5, 472–484. [Google Scholar] [CrossRef] [PubMed]
  8. D’Autreaux, M.B.; Toledano, M.B. ROS as Signalling Molecules: Mechanisms that Generate Specificity in ROS Homeostasis. Nat. Rev. Mol. Cell. Biol. 2007, 8, 813–824. [Google Scholar] [CrossRef] [PubMed]
  9. Trachootham, J.; Alexandre, J.; Huang, P. Targeting Cancer Cells by ROS-Mediated Mechanisms: A Radical Therapeutic Approach? Nat. Rev. Drug Discov. 2009, 8, 579–591. [Google Scholar] [CrossRef] [PubMed]
  10. Sies, H. Hydrogen Peroxide as a Central Redox Signaling Molecule in Physiological Oxidative Stress: Oxidative Eustress. Redox Biol. 2017, 11, 579–591. [Google Scholar] [CrossRef] [PubMed]
  11. Manchester, L.C.; Poeggeler, B.; Alvares, F.L.; Ogden, G.B.; Reiter, R.J. Melatonin Immunoreactivity in the Photosynthetic Prokaryote Rhodospirillum rubrum: Implications for an Ancient Antioxidant System. Cell. Mol. Biol. Res. 1995, 41, 391–395. [Google Scholar] [PubMed]
  12. Ma, Y.; Jiao, J.; Fan, X.; Sun, H.; Zhang, Y.; Jiang, J.; Liu, C. Endophytic Bacterium (Pseudomonas fluorescens RG11) May Transform Tryptophan to Melatonin and Promote Endogenous Melatonin Levels in the Roots of Four Grape Cultivars. Front. Plant Sci. 2016, 7, 2068. [Google Scholar] [CrossRef] [PubMed]
  13. Tan, D.X.; Hardeland, R.; Manchester, L.C.; Paredes, S.D.; Korkmaz, A.; Sainz, R.M.; Mayo, J.C.; Fuentes-Broto, L.; Reiter, R.L. The Changing Biological Roles of Melatonin during Evolution: From an Antioxidant to Signals of Darkness, Sexual Selection and Fitness. Biol. Rev. Camb. Philos. Soc. 2010, 85, 607–623. [Google Scholar] [CrossRef] [PubMed]
  14. Reiter, R.J.; Tan, D.X.; Galano, A. Melatonin: Exceeding Expectations. Physiology 2014, 29, 325–333. [Google Scholar] [CrossRef] [PubMed]
  15. Manchester, L.C.; Coto-Montes, A.; Boga, J.A.; Andersen, L.P.; Zhou, Z.; Galano, A.; Vriend, J.; Tan, D.X.; Reiter, R.J. Melatonin: An Ancient Molecule that Makes Oxygen Metabolically Tolerable. J. Pineal Res. 2015, 59, 403–419. [Google Scholar] [CrossRef] [PubMed]
  16. Reiter, R.J.; Fraschini, F. Endocrine Aspects of the Mammalian Pineal Gland. Neuroendocrinology 1969, 5, 219–255. [Google Scholar] [CrossRef] [PubMed]
  17. Su, S.C.; Hsieh, M.J.; Yang, M.E.; Chung, W.H.; Reiter, R.J.; Yang, S.F. Cancer Metastases: Mechanisms of Inhibition by Melatonin. J. Pineal Res. 2017, 62, e12370. [Google Scholar] [CrossRef] [PubMed]
  18. Cao, Z.; Fang, Y.; Lu, Y.; Tan, D.; Du, C.; Li, Y.; Ma, Q.; Yu, J.; Chen, M.; Zhou, C.; et al. Melatonin Alleviates Cadmium-induced Liver Injury by Inhibiting the TXNIP-NLRP3 Inflammasome. J. Pineal Res. 2017, 62, e12389. [Google Scholar] [CrossRef] [PubMed]
  19. Dubbels, R.; Reiter, R.J.; Klemke, E.; Goebel, A.; Schnakenberg, E.; Ehlers, C.; Schiwara, H.W.; Schloat, W. Melatonin in Edible Plants Identified by Radioimmunoassay and High Performance Liquid Chromatography-Mass Spectrometry. J. Pineal Res. 1995, 18, 28–31. [Google Scholar] [CrossRef] [PubMed]
  20. Hattori, A.; Migitaka, H.; Iigo, M.; Ito, M.; Yamamoto, K.; Ohtani-Kandro, G.; Hara, M.; Suzuki, T.; Reiter, R.J. Identification of Melatonin in Plants and Its Effects on Plasma Melatonin Levels and Binding to Melatonin Receptor in Vertebrates. Biochem. Mol. Biol. Int. 1995, 35, 627–634. [Google Scholar] [PubMed]
  21. Arnao, M.B.; Hernandez-Ruiz, J. Functions of Melatonin in Plants. J. Pineal Res. 2015, 59, 133–150. [Google Scholar] [CrossRef] [PubMed]
  22. Erland, L.A.; Murch, S.J.; Reiter, R.J.; Saxena, D.K. A New Balancing Act: The Many Roles of Melatonin and Serotonin in Plant Growth and Development. Plant Signal. Behav. 2015, 10, e1096469. [Google Scholar] [CrossRef] [PubMed]
  23. Reiter, R.J.; Tan, D.X.; Burkhardt, S.; Manchester, L.C. Melatonin in Plants. Nutr. Rev. 2001, 59, 286–290. [Google Scholar] [CrossRef] [PubMed]
  24. Lee, H.Y.; Back, K. Melatonin is Required for H2O2 and NO-mediated Defense Signaling through MAPKKK3 and OXI1 in Arabidopis thaliana. J. Pineal Res. 2017, 62, e12379. [Google Scholar] [CrossRef] [PubMed]
  25. Wei, Y.; Hu, W.; Wang, Q.; Zeng, H.; Li, X.; Yan, Y.; Reiter, R.J.; He, C.; Shi, H. Identification, Transcriptional and Functional Analysis of Heat-Shock Protein 90s in Banana (Musa acuminata L.) Highlight Their Novel Role in Melatonin-Mediated Plant Response to Fusarium Wilt. J. Pineal Res. 2017, 62, e12367. [Google Scholar] [CrossRef] [PubMed]
  26. Reiter, R.J.; Tan, D.X.; Zhou, Z.; Cruz, M.H.; Fuentes-Broto, L.; Galano, A. Phytomelatonin: Assisting Plants to Survive and Thrive. Molecules 2015, 20, 7396–7437. [Google Scholar] [CrossRef] [PubMed]
  27. Fridovich, I. Oxygen Toxicity: A Radical Explanation. J. Exp. Biol. 1998, 201, 1203–1209. [Google Scholar] [PubMed]
  28. Venegas, C.; Garcia, J.A.; Escames, G.; Ortiz, F.; Lopez, A.; Doerrier, C.; Garcia-Corzo, L.; Lopez, L.C.; Reiter, R.J.; Acuna-Castroviejo, D. Extrapineal Melatonin: Analysis of Its Subcellular Distribution and Daily Fluctuations. J. Pineal Res. 2012, 52, 217–227. [Google Scholar] [CrossRef] [PubMed]
  29. Van der Bliek, A.M.; Sedensky, M.M.; Morgan, P.G. Cell Biology of the Mitochondrion. Genetics 2017, 207, 843–871. [Google Scholar] [CrossRef] [PubMed]
  30. Reiter, R.J.; Mayo, J.C.; Tan, D.X.; Sainz, R.M.; Alatorre-Jimenez, M.; Qin, L. Melatonin as an Antioxidant: Under Promises but Over Delivers. J. Pineal Res. 2016, 61, 259–278. [Google Scholar] [CrossRef] [PubMed]
  31. Skinner, D.C.; Malpaux, B. High Melatonin Concentrations in the Third Ventricular Cerebrospinal Fluid are not Due to Galen Vein Blood Recirculating through the Choroid Plexus. Endocrinology 1999, 140, 4399–4405. [Google Scholar] [CrossRef] [PubMed]
  32. Brzezinski, A.; Seibel, M.M.; Lynch, H.J.; Deng, M.H.; Wurtman, R.J. Melatonin in Human Preovulatory Follicular Fluid. J. Clin. Endocrinol. Metab. 1987, 64, 865–867. [Google Scholar] [CrossRef] [PubMed]
  33. Tan, D.; Manchester, L.C.; Reiter, R.J.; Qi, W.; Hanes, M.A.; Farley, N.J. High Physiological Levels of Melatonin in the Bile of Mammals. Life Sci. 1999, 65, 2523–2529. [Google Scholar] [CrossRef]
  34. Stehle, J.H.; von Gall, C.; Korf, H.W. Melatonin: A Clock-output, A Clock-input. J. Neuroendocrinol. 2003, 15, 383–389. [Google Scholar] [CrossRef] [PubMed]
  35. Vaughan, G.M.; Pelham, R.W.; Pang, S.F.; Loughlin, L.L.; Wilson, K.M.; Sandock, K.L.; Vaughan, M.K.; Koslow, S.H.; Reiter, R.J. Nocturnal Elevation of Plasma Melatonin and Urinary 5-Hydroxyindoleacetic Acid in Young Men: Attempts at Modification by Brief Changes in Environmental Lighting and Sleep and by Autonomic Drugs. J. Clin. Endocrinol. Metab. 1976, 42, 752–764. [Google Scholar] [CrossRef] [PubMed]
  36. Cozzi, B.; Ravault, J.P.; Ferrandi, B.; Reiter, R.J. Melatonin Concentration in the Cerebral Vascular Sinuses of Sheep and Evidence for Its Episodic Release. J. Pineal Res. 1988, 5, 535–543. [Google Scholar] [CrossRef] [PubMed]
  37. Rousseau, A.; Petren, S.; Plannthin, J.; Eklundh, T.; Nordin, C. Serum and Cerebrospinal Fluid Concentrations of Melatonin: A Pilot Study in Healthy Male Volunteers. J. Neurol Transm. 1999, 106, 883–888. [Google Scholar] [CrossRef] [PubMed]
  38. Tamura, H.; Nakamura, Y.; Korkmaz, A.; Manchester, L.C.; Tan, D.X.; Sugino, N.; Reiter, R.J. Melatonin and the Ovary: Physiological and Pathophysiological Implications. Fertil. Steril. 2009, 92, 328–343. [Google Scholar] [CrossRef] [PubMed]
  39. Reiter, R.J.; Manchester, L.C.; Tan, D.X. Melatonin in Walnuts: Influence on Levels of Melatonin and Total Antioxidant Capacity of Blood. Nutrition 2005, 21, 920–924. [Google Scholar] [CrossRef] [PubMed]
  40. Troiani, M.E.; Reiter, R.J.; Tannenbaum, M.G.; Puig-Domingo, M.; Guerrero, J.M.; Menendez-Pelaez, A. Neither the Pituitary Gland nor the Sympathetic Nervous System is Responsible for Eliciting the Large Drop in Elevated Rat Pineal Melatonin Levels due to Swimming. J. Neural Transm. 1980, 74, 149–160. [Google Scholar] [CrossRef]
  41. Dauchy, R.T.; Wren-Dail, M.A.; Hoffman, A.E.; Hanifin, J.P.; Warfield, B.; Brainard, G.C.; Hill, S.M.; Belancio, V.P.; Dauchy, E.M.; Blask, D.E. Effects of Daytime Exposure to Light from Blue-Enriched Light-Emitting Diodes on the Nighttime Melatonin Amplitude and Circadian Regulation of Rodent Metabolism and Physiology. Comp. Med. 2016, 66, 373–383. [Google Scholar] [PubMed]
  42. Arendt, J. Melatonin. Clin. Endocrinol. 1988, 29, 205–229. [Google Scholar] [CrossRef]
  43. Tamura, H.; Takasaki, A.; Taketani, M.; Tanabe, M.; Lee, L.; Tamura, I.; Maekawa, R.; Aasada, H.; Yamagata, Y.; Sugino, N. Melatonin and Female Reproduction. J. Obstet. Gynaecol. Res. 2014, 40, 1–11. [Google Scholar] [CrossRef] [PubMed]
  44. Milan-Tomas, A.; Shapiro, C.M. Circadian Rhythm Disturbances in Alzheimer Disease: Current Concepts, Diagnosis, and Management. Alzheimer Dis. Assoc. Disord. 2018, in press. [Google Scholar] [CrossRef] [PubMed]
  45. Brainard, G.C.; Barker, P.M.; Hoffman, R.J.; Stetson, M.H.; Hanifin, J.P.; Podolin, P.L.; Rollag, M.D. Ultraviolet Regulation of Neuroendocrine and Circadian Physiology of Rodents. Vis. Res. 1994, 34, 1521–1533. [Google Scholar] [CrossRef]
  46. Tan, D.X.; Chen, L.D.; Poeggeler, B.; Manchester, L.C.; Reiter, R.J. Melatonin: A Potent Endogenous Hydroxyl Radical Scavenger. Endocrine 1993, 1, 57–60. [Google Scholar]
  47. Galano, A.; Tan, D.X.; Reiter, R.J. Melatonin as a Natural Ally against Oxidative Stress: A Physiochemical Examination. J. Pineal Res. 2011, 51, 1–16. [Google Scholar] [CrossRef] [PubMed]
  48. Boutin, J.A. Quinone Reductase 2 as a Promising Target of Melatonin Therapeutic Actions. Expert Opin. Ther. Targets 2016, 20, 303–317. [Google Scholar] [CrossRef] [PubMed]
  49. Reiter, R.J.; Tan, D.X.; Manchester, L.C.; Terron, M.P.; Flores, L.J.; Koppisepi, S. Medical Implications of Melatonin: Receptor-Mediated and Receptor-Independent Actions. Adv. Med. Sci. 2007, 52, 11–28. [Google Scholar] [PubMed]
  50. Barberino, R.S.; Menezes, V.G.; Ribeiro, A.E.A.S.; Palheta, R.C., Jr.; Jiang, X.; Smitz, J.E.J.; Matos, M.H.T. Melatonin Protects against Cisplatin-induced Ovarian Damage in Mice Via the MT1 Receptor and Antioxidant Activity. Biol. Reprod. 2017, 96, 1244–1255. [Google Scholar] [CrossRef] [PubMed]
  51. Deng, S.L.; Sun, T.C.; Yu, K.; Wang, Z.P.; Zhang, B.L.; Zhang, Y.; Wang, X.X.; Lian, Z.X.; Liu, Y.X. Melatonin Reduces Oxidative Damage and Upregulates Heat Shock Protein 80 Expression in Cryopreserved Human Semen. Free Radic. Biol. Med. 2017, 113, 347–354. [Google Scholar] [CrossRef] [PubMed]
  52. Stankov, B.; Reiter, R.J. Melatonin Receptors: Current Status, Facts and Hypotheses. Life Sci. 1990, 46, 971–982. [Google Scholar] [CrossRef]
  53. Dubocovich, M.L.; Delagrange, P.; Krause, D.N.; Sudgen, D.; Cardinali, D.P.; Olcese, J. International Union of Basic and Clinical Pharmacology. LXXV. Nomenclature, Classification, and Pharmacology of G Protein-coupled Melatonin Receptors. Pharmacol. Rev. 2010, 62, 343–380. [Google Scholar] [CrossRef] [PubMed]
  54. Wang, X.; Sirianni, A.; Pei, Z.; Cormier, K.; Smith, K.; Jiang, J.; Zhou, S.; Wang, H.; Zhao, R.; Yano, H.; et al. The Melatonin MT1 Receptor Axis Modulates Mutant Huntingtin-mediated Toxicity. J. Neurosci. 2011, 31, 14496–15507. [Google Scholar] [CrossRef] [PubMed]
  55. Urata, Y.; Honma, S.; Goto, S.; Todoroki, S.; Iida, T.; Cho, S.; Honma, K.; Kondo, T. Melatonin Induces Gamma-glutamylcysteine Synthetase Mediated by activator Protein-1 in Human Vascular Endothelial Cells. Free Radic. Bio. Med. 1999, 27, 838–847. [Google Scholar] [CrossRef]
  56. Ghosh, A.K.; Naaz, S.; Bhattacharjee, B.; Ghosal, N.; Chattopadhyay, A.; Roy, S.; Reiter, R.J.; Bandyopadhyay, D. Mechanism of Melatonin Protection against Copper-ascorbate-induced Oxidative Damage in Vitro through Isothermal Titration Calorimetry. Life Sci. 2017, 180, 123–136. [Google Scholar] [CrossRef] [PubMed]
  57. Tan, D.X.; Manchester, L.C.; Qin, L.; Reiter, R.J. Melatonin: A Mitochondrial Targeting Molecule Involving Mitochondrial Protection and Dynamics. Int. J. Mol. Sci. 2016, 17, 2124. [Google Scholar] [CrossRef] [PubMed]
  58. Back, K.; Tan, D.X.; Reiter, R.J. Melatonin Biosynthesis in Plants: Multiple Pathways Catalyze Tryptophan to Melatonin in Cytoplasm or Chloroplasts. J. Pineal Res. 2016, 61, 426–437. [Google Scholar] [CrossRef] [PubMed]
  59. Zheng, X.; Tan, D.X.; Allan, A.C.; Zuo, B.; Zhao, Y.; Reiter, R.J.; Wang, L.; Wang, Z.; Guo, Y.; Zhou, J.; et al. Chloroplastic Biosynthesis of Melatonin and Its Involvement in Protection of Plants from Salt Stress. Sci. Rep. 2017, 7, 41236. [Google Scholar] [CrossRef] [PubMed]
  60. Tan, D.X.; Hardeland, R.; Manchester, L.C.; Korkmaz, A.; Ma, S.; Rosales-Corral, S.; Reiter, R.J. Functional Roles of Melatonin in Plants, and Perspectives in Nutritional and Agricultural Science. J. Exp. Bot. 2012, 63, 577–597. [Google Scholar] [CrossRef] [PubMed]
  61. Champney, T.H.; Holtorf, A.P.; Steger, R.W.; Reiter, R.J. Concurrent Determination of Enzymatic Activities and Substrate Concentrations in the Melatonin Synthetic Pathway within the Same Rat Pineal Gland. J. Neurosci. Res. 1984, 11, 59–66. [Google Scholar] [CrossRef] [PubMed]
  62. Stehle, J.H.; Saade, A.; Rawashdeh, O.; Ackermann, K.; Jilg, A.; Sebesteny, T.; Maronde, E. A Survey of the Molecular Details in the Human Pineal Gland in the Light of Phylogeny, Structure, Function and Chronobiological Diseases. J. Pineal Res. 2011, 51, 17–43. [Google Scholar] [CrossRef] [PubMed]
  63. Pablos, M.I.; Reiter, R.J.; Ortiz, G.G.; Guerrero, J.M.; Agapito, M.T.; Chuang, J.I.; Sewerynek, E. Rhythms of Glutathione Peroxidase and Glutathione, Reductase in Brain of Chick and Their Inhibition by Light. Neurochem. Int. 1998, 32, 69–75. [Google Scholar] [CrossRef]
  64. Reiter, R.J.; Tan, D.X.; Rosales-Corral, S.; Manchester, L.C. The Universal Nature, Unequal Distribution and Antioxidant Functions of Melatonin and Its Derivatives. Mini-Rev. Med. Chem. 2013, 13, 373–384. [Google Scholar] [PubMed]
  65. Hardeland, R.; Fuhrberg, B.; Uria, H.; Behrmann, G.; Meyer, T.J.; Burkhardt, S.; Poeggeler, B. Chronobiology of Indoleamines in the Dinoflagellate Gonyaulax polyedra: Metabolism and Effects Related to Circadian Rhythmicity and Photoperiodism. Braz. J. Med. Biol. Res. 1996, 29, 119–123. [Google Scholar] [PubMed]
  66. Reczek, CR.; Chandel, N.S. ROS-dependent Signal Transduction. Curr. Opin. Cell Biol. 2014, 33C, 8–13. [Google Scholar] [CrossRef] [PubMed]
  67. Crow, J.P.; Spruel, C.; Chen, J.; Gunn, C.; Ischiropaulos, H.; Tsai, M.; Smith, C.D.; Koppenol, W.H.; Bechman, J.S. On the pH-dependent Yield of Hydroxyl Radical Products from Peroxynitrite. Free Radic. Biol. Med. 1994, 10, 331–338. [Google Scholar] [CrossRef]
  68. Hardeland, R. Neuroprotection by Radical Avoidance. Molecules 2009, 14, 5054–5102. [Google Scholar] [CrossRef] [PubMed]
  69. Korkmaz, A.; Reiter, R.J.; Topal, T.; Manchester, L.C.; Oter, S.; Tan, D.X. Melatonin: An Established Antioxidant Worthy of Its Use in Clinical Trials. Mol. Med. 2009, 15, 43–50. [Google Scholar] [PubMed]
  70. Brazao, V.; Santello, F.H.; Colato, R.P.; Mazotti, T.T.; Tazinafo, L.F.; Toldo, M.P.A.; do Vale, G.T.; Tirapelli, C.R.; do Prado, J.C., Jr. Melatonin: Antioxidant and Modulatory Properties in Age-related Changes during Trypanosoma cruzi Infection. J. Pineal Res. 2017, 63, e12409. [Google Scholar] [CrossRef] [PubMed]
  71. Reiter, R.J.; Rosales-Corral, S.; Tan, D.X.; Jou, M.J.; Galano, A.; Xu, B. Melatonin as a Mitochondria-targeted Antioxidant: One of Evolution’s Best Ideas. Cell. Mol. Life Sci. 2017, 74, 3863–3881. [Google Scholar] [CrossRef] [PubMed]
  72. Barlow-Walden, L.R.; Reiter, R.J.; Abe, M.; Pablos, M.I.; Menendez-Pelaez, A.; Chen, L.R.; Poeggeler, B. Melatonin Stimulates Brain Glutathione Peroxidase Activity. Neurochem. Int. 1995, 26, 497–502. [Google Scholar] [CrossRef]
  73. Reiter, R.J.; Tan, D.X.; Osuna, C.; Gitto, E. Actions of Melatonin in the Reduction of Oxidative Stress. J. Biomed. Sci. 2000, 7, 444–458. [Google Scholar] [CrossRef] [PubMed]
  74. Ma, Q.; Zhang, T.; Zhang, P.; Wang, Z.Y. Melatonin Attenuates Postharvest Physiological Deterioration of Cassava Storage Roots. J. Pineal Res. 2016, 60, 424–434. [Google Scholar] [CrossRef] [PubMed]
  75. Sung, J.H.; Cho, E.H.; Kim, M.O.; Koh, P.O. Identification of Protein Differentially Expressed by Melatonin Treatment in Cerebral Ischemic Injury—A Proteomics Approach. J. Pineal Res. 2009, 46, 300–306. [Google Scholar] [CrossRef] [PubMed]
  76. Mendez, I.; Vazquez-Martinez, O.; Hernandez-Munoz, R.; Valente-Godinez, H.; Diaz-Munoz, M. Redox Regulation and Pro-oxidant Reactions in the Physiology of Circadian Systems. Biochimie 2015, 124, 178–186. [Google Scholar] [CrossRef] [PubMed]
  77. Vriend, J.; Reiter, R.J. Melatonin, Bone Regulation and the Ubiquitin-Proteasome Connection: A Review. Life Sci. 2016, 145, 152–160. [Google Scholar] [CrossRef] [PubMed]
  78. Janjetovic, Z.; Jarrett, S.G.; Lee, E.F.; Duprey, C.; Reiter, R.J.; Slominski, A. Melatonin and Its Metabolites Protect Human Melanocytes against UVB-induced Damage: Involvement of Nrf2-mediated Pathways. Sci. Rep. 2017, 7, 1274. [Google Scholar] [CrossRef] [PubMed]
  79. Brand, M.D. The Sites and Topology of Mitochondrial Superoxide Production. Exp. Gerontol. 2010, 45, 466–472. [Google Scholar] [CrossRef] [PubMed]
  80. Sousa, J.S.; D’Imprima, E.; Vonck, J. Mitochondrial Respiratory Chain Complexes. Subcell. Biochem. 2018, 87, 167–227. [Google Scholar] [PubMed]
  81. Muller, F.L.; Liu, Y.; Van Rammen, H. Complex III Releases Superoxide to Both Sides of the Inner Mitochondrial Membrane. J. Biol. Chem. 2004, 279, 49064–49073. [Google Scholar] [CrossRef] [PubMed]
  82. Seva, L.A.; Chandel, N.S. Physiological Roles of Mitochondrial Reactive Oxygen Species. Mol. Cell. 2012, 48, 158–167. [Google Scholar]
  83. Kalous, M.; Drahota, Z. The Role of Mitochondria in Aging. Physiol. Res. 1996, 45, 351–359. [Google Scholar] [PubMed]
  84. Kauppila, T.E.S.; Kauppila, J.H.K.; Larsson, N.G. Mammalian Mitochondria and Aging: An Update. Cell. Metab. 2017, 25, 57–71. [Google Scholar] [CrossRef] [PubMed]
  85. Rosales-Corral, S.A.; Acuna-Castroviejo, D.; Coto-Montes, A.; Boga, J.A.; Manchester, L.C.; Fuentes-Broto, L.; Korkmaz, A.; Ma, S.; Tan, D.X.; Reiter, R.J. Alzheimer’s Disease: Pathophysiological Mechanisms and the Beneficial Role of Melatonin. J. Pineal Res. 2012, 52, 167–202. [Google Scholar] [CrossRef] [PubMed]
  86. Coto-Montes, A.; Boga, J.A.; Tan, D.X.; Reiter, R.J. Melatonin as a Potential Agent in the Treatment of Sacropenia. In, J. Mol. Sci. 2016, 17, E1771. [Google Scholar] [CrossRef] [PubMed]
  87. Acuna-Castroviejo, D.; Rahim, I.; Acuna-Fernandez, C.; Fernandez-Ortiz, M.; Solera-Marin, J.; Sayed, R.K.A.; Diaz-Casado, M.E.; Dusanova, I.; Lopez, L.C.; Escames, G. Melatonin, Clock Genes and Mitochondria in Sepsis. Cell. Mol. Life Sci. 2017, 74, 3965–3988. [Google Scholar] [CrossRef] [PubMed]
  88. Cardinali, D.P.; Vigo, D.E. Melatonin, Mitochondria and Metabolic Syndrome. Cell. Mol. Life Sci. 2017, 74, 3941–3954. [Google Scholar] [CrossRef] [PubMed]
  89. Kanaan, G.N.; Harper, M.E. Cellular Redox Dysfunction in the Development of Cardiovascular Diseases. Biochem. Biophys. Acta 2017, 1861, 2822–2829. [Google Scholar] [CrossRef] [PubMed]
  90. Drummond, G.R.; Selemidis, S.; Griendling, K.K.; Sobey, C.G. Combatting Oxidative Stress in Vascular Disease: NADPH Oxidases as Therapeutic Targets. Nat. Rev. Drug Discov. 2011, 10, 453–471. [Google Scholar] [CrossRef] [PubMed]
  91. Krause, K.H. Aging: A Revisited Theory Based on Free Radicals Generated by NOX Family NADPH Oxidases. Exp. Gerontol. 2007, 42, 256–262. [Google Scholar] [CrossRef] [PubMed]
  92. Vida, C.; Corpas, I.; De la Fuente, M.; Gonzalez, E.M. Age-related Changes in Xanthine Oxidase Activity and Lipid Peroxidation as well as in the Correlation between Both Parameters, in Plasma and Several Organs from Female Mice. J. Physiol. Biochem. 2011, 67, 551–558. [Google Scholar] [CrossRef] [PubMed]
  93. Alper, G.; Girgin, F.K.; Ozgonul, M.; Mentes, G.; Erroz, B. MAO Inhibitors and Oxidative Stress in Aging Brain Tissue. Eur. Neuropsychopharmacol. 1999, 9, 247–252. [Google Scholar] [CrossRef]
  94. Naskar, A.; Prabhakar, V.; Singh, R.; Dutta, D.; Mohanakumar, K.P. Melatonin Enhances L-DOPA Therapeutic Effects, Helps to Reduce Its Dose, and Protects Dopaminergic Neurons in 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine-induced Parkinsonism in Mice. J. Pineal Res. 2015, 58, 262–274. [Google Scholar] [CrossRef] [PubMed]
  95. Diaz-Casado, M.E.; Lima, E.; Garcia, J.A.; Doerrier, C.; Aranda, P.; Sayed, R.K.A.; Guerra-Librero, A.; Escames, G.; Lopez, L.C.; Acuna-Castroviejo, D. Melatonin Rescues Zebrafish Embryos from the Parkinsonian Phenotype Restoring the Parkin/PINK1/DJ-1/MUL1 Network. J. Pineal Res. 2016, 61, 96–107. [Google Scholar] [CrossRef] [PubMed]
  96. Titorenko, V.I.; Terlecky, S.R. Peroxisome Metabolism and Cellular Aging. Traffic 2011, 12, 252–259. [Google Scholar] [CrossRef] [PubMed]
  97. Legakis, J.E.; Koepke, J.I.; Jedeszko, C.; Barlaskar, F.; Terlecky, L.J.; Edwards, H.J.; Walton, P.A.; Terlecky, S.R. Peroxisome Senescence in Human Fibroblasts. Mol. Biol. Cell 2002, 13, 4243–4255. [Google Scholar] [CrossRef] [PubMed]
  98. Terman, A.; Kurz, T.; Navratil, M.; Arriaga, E.A.; Brunk, U.T. Mitochondrial Turnover and Aging of Long-lived Postmitotic Cells: The Mitochondrial-lysosomal Axis Theory of Aging. Antioxid. Redox Signal. 2010, 12, 503–535. [Google Scholar] [CrossRef] [PubMed]
  99. Huo, X.; Wang, C.; Yu, Z.; Peng, Y.; Wang, S.; Feng, S.; Zhang, S.; Tian, X.; Sun, C.; Liu, K.; et al. Human Transporters, PEPT 1/2, Facilitate Melatonin Transportation into Mitochondria of Cancer Cells: An Implication of the Therapeutic Potential. J. Pineal Res. 2017, 62, e12390. [Google Scholar] [CrossRef] [PubMed]
  100. Tan, D.X.; Manchester, L.C.; Liu, X.; Rosales-Corral, S.A.; Acuna-Castroviejo, D.; Reiter, R.J. Mitochondria and Chloroplasts as the Original Sites of Melatonin Synthesis: A Hypothesis Related to Melatonin’s Primary Function and Evolution in Eukaryotes. J. Pineal Res. 2013, 54, 127–138. [Google Scholar] [CrossRef] [PubMed]
  101. Wang, L.; Feng, C.; Zhang, X.; Guo, Y.; Zhou, F.; Shan, D.; Liu, X.; Kong, J. Plant Mitochondria Synthesize Melatonin and Enhance the Tolerance of Plants to Drought Stress. J. Pineal Res. 2017, 63, e12429. [Google Scholar] [CrossRef] [PubMed]
  102. Suofu, Y.; Li, W.; Jean-Alphonse, F.G.; Jia, J.; Khattar, N.K.; Li, J.; Baranov, S.V.; Leronni, D.; Mihalik, A.C.; He, Y.; et al. Dual Role of Mitochondria in Producing Melatonin and Driving GPCR Signaling to Block Cytochrome c Release. Proc. Natl. Acad. Sci. USA 2017, 114, E7997–E8006. [Google Scholar] [CrossRef] [PubMed]
  103. Menendez-Pelaez, A.; Reiter, R.J. Distribution of Melatonin in Mammalian Tissues: Relative Importance of Nuclear Versus Cytosolic Localization. J. Pineal Res. 1993, 15, 59–69. [Google Scholar] [CrossRef] [PubMed]
  104. Paradies, G.; Paradies, V.; Ruggiero, F.M.; Petrosillo, G. Mitochondrial Bioenergetics Decay in Aging: Beneficial Effects of Melatonin. Cell. Mol. Life Sci. 2017, 74, 3897–3911. [Google Scholar] [CrossRef] [PubMed]
  105. Quintana, L.; Cobrera, J.; Perdomo, J.; Estevez, F.; Loro, J.F.; Reiter, R.J.; Quintana, J. Melatonin Enhances Hypothermia-induced Apoptotic Cell Death in Human Leukemia Cells. J. Pineal Res. 2016, 61, 381–395. [Google Scholar] [CrossRef] [PubMed]
  106. Ding, M.; Ning, J.; Feng, N.; Li, Z.; Liu, Z.; Wang, Y.; Li, X.; Hue, C.; Jia, X.; Xu, R.; et al. Dynamin-related Protein-1-mediated Mitochondrial Fission Contributes to Post-traumatic Cardiac Dysfunction in Rats and the Protective Effect of Melatonin. J. Pineal Res. 2017, 63, e12447. [Google Scholar] [CrossRef] [PubMed]
  107. Kleszczyriski, K.; Zillikens, D.; Fischer, T.W. Melatonin Enhances Mitochondrial ATP Synthesis, Reduces Reactive Oxygen Species Formation, and Mediates Translocation of the Nuclear Erythroid 2-related Factor 2 in Activation of Phase-2 Antioxidant Enzymes (γ-GCS, HO-1, NQO1) in Ultraviolet Radiation-treated Normal Human Epidermal Keratinocytes (NHEK). J. Pineal Res. 2016, 61, 187–197. [Google Scholar]
  108. Areti, A.; Komirishetty, P.; Akuthota, M.; Malik, R.A.; Kurman, A. Melatonin Prevents Mitochondrial Dysfunction and Promotes Neuroprotection by Inducing Autophagy during Oxaliplatin-evoked Peripheral Neuropathy. J. Pineal Res. 2017, 62, e12393. [Google Scholar] [CrossRef] [PubMed]
  109. Dehdashtian, E.; Mehrzadi, S.; Yousefi, B.; Hosseinzadeh, A.; Reiter, R.J.; Ghaznavi, H.; Naseripour, M. Diabetic Retinopathy Pathogenesis and the Ameliorating Effects of Melatonin: Involvement of Autophagy, Inflammation and Oxidative Stress. Life Sci. 2018, 193, 20–33. [Google Scholar] [CrossRef] [PubMed]
  110. Das, N.; Mandala, A.; Naaz, S.; Giri, S.; Jain, M.; Bandyopadhyay, D.; Reiter, R.J.; Roy, S.S. Melatonin Protects against Lipid-induced Mitochondrial Dysfunction in Hepatocytes and Inhibits Stellate Cell Activation during Hepatic Fibrosis in Mice. J. Pineal Res. 2017, 62, e12404. [Google Scholar] [CrossRef] [PubMed]
  111. Dragicevic, N.; Copes, N.; O’Neal-Moffitt, G.; Jin, J.; Buzzeo, R.; Mamcarz, M.; Tan, J.; Cao, C.; Olcese, J.J.; Arendash, G.W.; et al. Melatonin Treatment Restores Mitochondrial Function in Alzheimer’s Mice: A Mitochondrial Protective Role of Melatonin Membrane Receptor Signaling. J. Pineal Res. 2011, 51, 75–86. [Google Scholar] [CrossRef] [PubMed]
  112. Xu, S.; Pi, H.; Zhang, L.; Zhang, N.; Li, Y.; Zhang, H.; Tang, J.; Li, H.; Feng, M.; Deng, P.; et al. Melatonin Prevents Abnormal Mitochondrial Dynamics Resulting from Neurotoxicity of Cadmium by Blocking Cadmium-dependent Translocation of Drp1 to the Mitochondria. J. Pineal Res. 2016, 60, 291–302. [Google Scholar] [CrossRef] [PubMed]
  113. Melchiorri, D.; Reiter, R.J.; Attica, A.M.; Hara, M.; Burgas, A.; Nistico, G. Potent Protective Effect of Melatonin on in Vivo Paraquat-induced Oxidative Damage in Rats. Life Sci. 1995, 56, 83–89. [Google Scholar] [CrossRef]
  114. Maity, P.; Bindu, S.; Dey, S.; Goyal, M.; Alam, A.; Pal, C.; Reiter, R.J.; Bandyopadhaya, D. Melatonin Reduces Indomethacin-induced Gastric Mucosal Cell Apoptosis in Preventing Mitochondrial Oxidative Stress and the Activation of Mitochondrial Pathway of Apoptosis. J. Pineal Res. 2009, 46, 314–323. [Google Scholar] [CrossRef] [PubMed]
  115. Chuang, J.I.; Pan, I.L.; Hsieh, C.Y.; Huang, C.Y.; Chen, P.C.; Shin, J.W. Melatonin Prevents the Dynamin-related Protein 1-dependent Mitochondrial Fission and Oxidative Insult in the Cortical Neurons after 1-Methyl-4-phenylpyridinium Treatment. J. Pineal Res. 2016, 61, 230–240. [Google Scholar] [CrossRef] [PubMed]
  116. Pei, H.F.; Hou, J.N.; Wei, F.P.; Xue, Q.; Zhang, F.; Peng, C.F.; Yang, Y.; Tian, Y.; Feng, J.; Du, J.; et al. Melatonin Attenuates Postmyocardial Infarction Injury Via Increasing Tom70 Expression. J. Pineal Res. 2017, 62, e12371. [Google Scholar] [CrossRef] [PubMed]
  117. Antoniou, C.; Chatzimichail, G.; Xenofontos, R.; Pavlou, J.J.; Panagiotou, E.; Christou, A.; Fotopoulos, V. Melatonin Systemically Ameliorates Drought Stress-induced Damage in Medicago sativa Plants by Modulating Nitro-oxidative Homeostasis and Proline Metabolism. J. Pineal Res. 2017, 62, e12401. [Google Scholar] [CrossRef] [PubMed]
  118. Galano, A.; Tan, D.X.; Reiter, R.J. Melatonin and Related Compounds: Chemical Insights into Their Protective Effects against Oxidative Stress. Curr. Org. Chem. 2017, 21, 2077–2095. [Google Scholar] [CrossRef]
  119. Galano, A. On the Direct Scavenging Activity of Melatonin towards Hydroxyl and a Series of Peroxyl Radicals. Phys. Chem. Chem. Phys. 2011, 13, 7178–7188. [Google Scholar] [CrossRef] [PubMed]
  120. Tan, D.X.; Manchester, L.C.; Reiter, R.J.; Qi, W.; Karbownik, M.; Calvo, J.R. Significance of Melatonin in Antioxidative Defense System: Reactions and Products. Biol. Signals Recept. 2000, 9, 137–159. [Google Scholar] [CrossRef] [PubMed]
  121. Hardeland, R. Antioxidative Protection by Melatonin: Multiplicity of Mechanisms from Radical Detoxification to Radical Avoidance. Endocrine 2005, 27, 119–130. [Google Scholar] [CrossRef]
  122. Rodriguez, C.; Mayo, J.C.; Sainz, R.M.; Antolin, I.; Herrera, F.; Martin, V.; Reiter, R.J. Regulation of Antioxidant Enzymes: A Significant Role for Melatonin. J. Pineal Res. 2004, 36, 1–9. [Google Scholar] [CrossRef] [PubMed]
  123. Paredes, S.D.; Bejarano, I.; Terron, M.P.; Berriga, C.; Reiter, R.J.; Rodriguez, A.B. Melatonin and Tryptophan Counteract Lipid Peroxidation and Modulate Superoxide Dismutase Activity in Heterophils In Vivo: Effect of Antigen-induced Activation and Age. Age 2009, 31, 379–388. [Google Scholar] [CrossRef] [PubMed]
  124. Yu, L.; Fan, C.; Li, Z.; Zhang, J.; Xue, X.; Zhao, G.; Yang, Y.; Wang, H. Melatonin Rescues Cardiac Thioredoxin during Ischemia-reperfusion Injury in Acute Hyperglycemic State by Restoring Notch1/Hes1/Akt Signaling in a Membrane Receptor-dependent Manner. J. Pineal Res. 2017, 62, e12375. [Google Scholar] [CrossRef] [PubMed]
  125. Han, L.; Wang, H.; Li, L.; Li, X.; Ge, J.; Reiter, R.J.; Wang, Q. Melatonin Protects Against Maternal Obesity-associated Oxidative Stress and Meiotic Defects in Oocytes Via SIRT3-SOD2-dependent Pathways. J. Pineal Res. 2017, 63, e12431. [Google Scholar] [CrossRef] [PubMed]
  126. Reiter, R.J.; Rosales-Corral, S.; Zhou, X.; Tan, D.X. Role of SIRT3/SOD2 Signaling in Mediating the Antioxidant Actions of Melatonin in Mitochondria. Curr. Trends Endocrinol. 2017, 9, 45–49. [Google Scholar]
  127. Zhai, M.; Li, B.; Duan, W.; Jing, L.; Zhang, B.; Zhang, M.; Yu, L.; Liu, Z.; Yu, B.; Ren, K.; et al. Melatonin Ameliorates Myocardial Ischemia Reperfusion Injury Through SIRT3-dependent Regulation of Oxidative Stress and Apoptosis. J. Pineal Res. 2017, 63, e12433. [Google Scholar] [CrossRef] [PubMed]
  128. Jimenez-Aranda, A.; Fernandez-Vasquez, G.; Mohammad A-Serrano, M.; Reiter, R.J.; Agil, A. Melatonin Improves Mitochondrial Function in Inguinal White Adipose Tissue of Zucker Diabetic Rats. J. Pineal Res. 2014, 57, 103–109. [Google Scholar] [CrossRef] [PubMed]
  129. Lee, M.S.; Yin, T.C.; Sung, P.H.; Chiang, J.Y.; Sun, C.K.; Yip, H.K. Melatonin Enhances Survival and Reserves Functional Integrity of Stem Cells: A Survey. J. Pineal Res. 2017, 62, e12372. [Google Scholar] [CrossRef] [PubMed]
  130. Cai, S.Y.; Zhang, Y.; Xu, Y.P.; Qi, Z.Y.; Li, M.Q.; Ahammed, G.J.; Xia, X.J.; Shi, K.; Zhou, Y.H.; Reiter, R.J.; et al. HsfA1a Upregulates Melatonin Biosynthesis to Confer Cadmium Tolerance in Tomato Plants. J. Pineal Res. 2017, 62, e12387. [Google Scholar] [CrossRef] [PubMed]
  131. Ma, Z.; Xin, Z.; Di, W.; Yan, X.; Li, X.; Reiter, R.J.; Yang, Y. Melatonin and Mitochondrial Function during Ischemia/Reperfusion Injury. Cell. Mol. Life Sci. 2017, 72, 3989–3998. [Google Scholar] [CrossRef] [PubMed]
  132. Hardeland, R.; Tan, D.X.; Reiter, R.J. Kynuramines Metabolites of Melatonin and Other Indoles: The Resurrection of an Almost Forgotten Class of Biogenic Amines. J. Pineal Res. 2009, 47, 109–126. [Google Scholar] [CrossRef] [PubMed]
  133. Galano, A.; Tan, D.X.; Reiter, R.J. On the Free Radical Scavenging Activities of Melatonin’s Metabolites, AFMK and AMK. J. Pineal Res. 2013, 54, 245–257. [Google Scholar] [CrossRef] [PubMed]
  134. Tan, D.X.; Manchester, L.C.; Terron, M.P.; Flores, L.J.; Reiter, R.J. One Molecule, Many Derivatives: A Never Ending Interaction of Melatonin with Reactive Oxygen and Nitrogen Species? J. Pineal Res. 2007, 42, 28–42. [Google Scholar] [CrossRef] [PubMed]
  135. Tan, D.X.; Hardeland, R.; Manchester, L.C.; Galano, A.; Reiter, R.J. Cyclic 3-hydroxy-melatonin (C3OHM), a Potent Antioxidant, Scavenges Free Radicals and Suppresses Oxidative Reactions. Curr. Med. Chem. 2014, 21, 1557–1585. [Google Scholar] [CrossRef] [PubMed]
  136. Galano, A.; Medina, M.E.; Tan, D.X.; Reiter, R.J. Melatonin and Its Metabolites as Cooper Chelating Agents and their Role in Inhibiting Oxidative Stress: a Physiochemical Analysis. J. Pineal Res. 2015, 58, 107–116. [Google Scholar] [CrossRef] [PubMed]
  137. Alvarez-Diduk, R.; Galano, A.; Tan, D.X.; Reiter, R.J. N-acetylserotonin and 6-hydroxy-melatonin Against Oxidative Stress: Implications for the Overall Protection Exerted by Melatonin. J. Phys. Chem. B 2015, 119, 8535–8543. [Google Scholar] [CrossRef] [PubMed]
  138. Majidinia, M.; Sadeghpour, A.; Mehrzadi, S.; Reiter, R.J.; Khatami, N.; Yousefi, B. Melatonin: A Pleiotropic Molecule that Modulates DNA Damage Response and Repair Pathways. J. Pineal Res. 2017, 63, e12416. [Google Scholar] [CrossRef] [PubMed]
  139. Jou, M.J.; Peng, T.I.; Reiter, R.J.; Jou, S.B.; Wu, H.Y.; Wen, S.T. Visualization of the Antioxidant Effects of Melatonin at the Mitochondrial Level during Oxidative Stress-induced Apoptosis of Rat Brain Astrocytes. J. Pineal Res. 2004, 37, 55–70. [Google Scholar] [CrossRef] [PubMed]
  140. Jou, M.J.; Peng, T.I.; Hsu, L.F.; Jou, S.B.; Reiter, R.J.; Yang, C.M.; Chiao, C.C.; Lin, Y.F.; Chen, C.C. Visualization of Melatonin’s Multiple Mitochondrial Levels of Protection Against Mitochondrial Ca2+-mediated Permeability Transition and Beyond in Rat Brain Astrocytes. J. Pineal Res. 2010, 48, 20–38. [Google Scholar] [CrossRef] [PubMed]
  141. Peng, T.I.; Hsiao, C.W.; Reiter, R.J.; Tanaka, M.; Lai, Y.K.; Jou, M.J. mtDNA T8993G Mutation-induced Mitochondrial Complex V Inhibition Augments Cardiolipin-dependent Alterations in Mitochondrial Dynamics during Oxidative, Ca2+, and Lipid Insults in NARP Cybrids: A Potential Therapeutic Target for Melatonin. J. Pineal Res. 2012, 52, 93–106. [Google Scholar] [CrossRef] [PubMed]
  142. Reiter, R.J.; Paredes, S.D.; Korkmaz, A.; Jou, M.J.; Tan, D.X. Melatonin Combats Molecular Terrorism at the Mitochondrial Level. Interdiscip. Toxicol. 2008, 1, 127–149. [Google Scholar] [CrossRef] [PubMed]
  143. Martin, M.; Macias, M.; Escames, G.; Reiter, R.J.; Agapita, M.T.; Ortiz, G.G.; Acuna-Castroviejo, D. Melatonin-induced Increased Activity of the Respiratory Chain Complexes I and IV can Prevent Mitochondrial Damage Induced by Ruthenium Red In Vivo. J. Pineal Res. 2000, 28, 242–248. [Google Scholar] [CrossRef] [PubMed]
  144. Martin, M.; Macias, M.; Escames, G.; Leon, J.; Acuna-Castroviejo, D. Melatonin but not Vitamins C and E Maintains Glutathione Homeostasis in Butyl-hydroperoxide-induced Mitochondrial Oxidative Stress. FASEB J. 2000, 14, 1677–1679. [Google Scholar] [CrossRef] [PubMed]
  145. Acuna-Castroviejo, D.; Lopez, L.C.; Escames, G.; Lopez, A.; Garcia, J.A.; Reiter, R.J. Melatonin-mitochondria Interplay in Health and Disease. Curr. Top. Med. Chem. 2011, 11, 221–240. [Google Scholar] [CrossRef] [PubMed]
  146. Choi, G.H.; Lee, H.Y.; Back, K. Chloroplast Overexpression of Rice Caffeic Acid O-methyltransferase Increases Melatonin Production in Chloroplasts Via 5-methoxytryptamine Pathway in Transgenic Rice Plants. J. Pineal Res. 2017, 63, 12412. [Google Scholar] [CrossRef] [PubMed]
  147. Hardeland, R. Melatonin and the Electron Transport Chain. Cell. Mol. Life Sci. 2017, 71, 3883–3896. [Google Scholar] [CrossRef] [PubMed]
  148. Hedlund, L.; Lischko, M.M.; Rollag, M.D.; Niswender, G.D. Melatonin: Daily Cycle in Plasma and Cerebrospinal Fluid in Calves. Science 1977, 195, 686–687. [Google Scholar] [CrossRef] [PubMed]
  149. Tricoire, H.; Locatelli, A.; Chemineau, P.; Malpaux, B. Melatonin Enters the Cerebrospinal Fluid through the Pineal Recess. Endocrinology 2002, 143, 84–90. [Google Scholar] [CrossRef] [PubMed]
  150. Reiter, R.J.; Tan, D.X.; Kim, S.J.; Cruz, M.H.C. Delivery of Pineal Melatonin to the brain and SCN: Role of Canaliculi, Cerebrospinal Fluid, Tanycytes and Virchow-Robin Perivascular Spaces. Brain Struct. Funct. 2014, 219, 1873–1887. [Google Scholar] [CrossRef] [PubMed]
  151. Mayo, J.C.; Sainz, R.M.; Gonzalez-Menendez, P.; Hevia, D.; Cermuda-Cermuda, R. Melatonin Transplant into Mitochondria. Cell. Mol. Life Sci. 2017, 74, 3927–3940. [Google Scholar] [CrossRef] [PubMed]
  152. Hevia, D.; Gonzalez-Menendez, P.; Quiros-Gonzales, I.; Miar, A.; Rodriguez-Garcia, A.; Tan, D.X.; Reiter, R.J.; Mayo, J.C.; Sainz, R.M. Melatonin Uptake through Glucose Transporters: A New Target for Melatonin Inhibition of Cancer. J. Pineal Res. 2015, 58, 234–250. [Google Scholar] [CrossRef] [PubMed]
  153. Lowes, D.A.; Webster, N.R.; Murphy, M.P.; Galley, H.F. Antioxidants that Protect Mitochondria Reduce Interleukin-6 and Oxidative Stress, Improve Mitochondrial Function, and Reduce Biochemical Markers of Organ Dysfunction in a Rat Model of sepsis. Br. J. Anaesth. 2013, 110, 472–480. [Google Scholar] [CrossRef] [PubMed]
  154. Esteban-Zubero, E.; Alatorre-Jimenez, M.A.; Lopez-Pingarron, L.; Reyes-Gonzalez, M.C.; Almeida-Sauza, P.; Cantin-Golet, A.; Ruiz-Ruiz, F.J.; Tan, D.X.; Garcia, J.J.; Reiter, R.J. Melatonin’s Role in Preventing Toxin-related and Sepsis-mediated Hepatic Damage: A Review. Pharmacol. Res. 2016, 105, 108–120. [Google Scholar] [CrossRef] [PubMed]
  155. Hu, W.; Deng, C.; Ma, Z.; Wang, D.; Fan, C.; Li, T.; Di, S.; Gong, B.; Reiter, R.J.; Yang, Y. Utilizing Melatonin to Combat Bacterial Infections, and Septic Injury. Br. J. Pharmacol. 2017, 174, 754–788. [Google Scholar] [CrossRef] [PubMed]
  156. Gitto, E.; Karbownik, M.; Reiter, R.J.; Tan, D.X.; Cuzzocrea, S.; Chiurazzi, P.; Cordaro, S.; Corona, G.; Trimarchi, G.; Barberi, I. Effects of Melatonin Treatment in Septic Newborns. Pediatr. Res. 2001, 50, 756–760. [Google Scholar] [CrossRef] [PubMed]
  157. Mayo, J.C.; Sainz, R.M.; Gonzalez-Menendez, P.; Cepas, V.; Tan, D.X.; Reiter, R.J. Melatonin and Sirtuins: A Not-so Unexpected Relationship. J. Pineal Res. 2017, 62, e12391. [Google Scholar] [CrossRef] [PubMed]
  158. Byeon, Y.; Back, K. Melatonin Production in Escherichia coli by Dual Expression of Serotonin N-acetyltransferase and Caffeic Acid O-Methyltransferase. Appl. Microbiol. Biotechnol. 2016, 100, 6683–6691. [Google Scholar] [CrossRef] [PubMed]
  159. Zimorski, V.; Ku, C.; Martin, W.F.; Gould, S.B. Endosymbiotic Theory for Organelle Origins. Curr. Opin. Microbiol. 2014, 22, 38–48. [Google Scholar] [CrossRef] [PubMed]
  160. He, C.; Wang, J.; Zhang, Z.; Yang, M.; Li, Y.; Tian, X.; Ma, T.; Tao, J.; Zhu, K.; Song, Y.; et al. Mitochondria Synthesize Melatonin to Ameliorate Its Function and Improve Oocyte Quality Under In Vitro Conditions. Int. J. Mol. Sci. 2016, 17, 939. [Google Scholar] [CrossRef] [PubMed]
  161. Lee, H.Y.; Back, B. Cadmium Disrupts Subcellular Organelles, Including Chloroplasts, Resulting in Melatonin Induction in Plants. Molecules 2017, 22, E1791. [Google Scholar] [CrossRef] [PubMed]
  162. Byeon, Y.; Lee, H.Y.; Back, K. Chloroplastic and Cytoplasmic Overexpression of Sheep Serotonin N-acetyltransferase in Transgenic Rice Plants is Associated with Low Melatonin Production Despite High Enzyme Activity. J. Pineal Res. 2015, 58, 461–464. [Google Scholar] [CrossRef] [PubMed]
  163. Ganguly, S.; Gastel, J.A.; Weller, J.L.; Schwartz, C.; Jaffe, H.; Namboodiri, M.A.; Coon, S.L.; Hoffman, A.B.; Rollag, M.; Obsil, T.; et al. Melatonin Synthesis: 14–3-3-dependent Activation and Inhibition of Arylalkylamine N-acetyltransferase Mediated by Phosphoserine-205. Proc. Natl. Acad. Sci. USA 2005, 102, 1222–1227. [Google Scholar] [CrossRef] [PubMed]
  164. Wei, Y.; Chang, Y.; Zeng, H.; Liu, G.; He, C.; Shi, H. RAV Transcription Factors are Essential for Disease Resistance Against Cassava Bacterial Blight Via Activation of Melatonin Biosynthesis Genes. J. Pineal Res. 2017, in press. [Google Scholar] [CrossRef] [PubMed]
  165. Li, M.Q.; Hasan, M.K.; Li, C.X.; Ahammed, G.J.; Xia, X.J.; Shi, K.; Zhou, V.H.; Reiter, R.J.; Yu, J.Q.; Xu, M.X.; et al. Melatonin Mediates Selenium-induced Tolerance to Cadmium Stress in Tomato Plants. J. Pineal Res. 2016, 61, 291–302. [Google Scholar] [CrossRef] [PubMed]
  166. Chan, Z.; Shi, H. Improved Abiotic Tolerance of Bermudagrass by Exogenous Small Molecules. Front. Signal. Behav. 2015, 10, e971577. [Google Scholar] [CrossRef] [PubMed]
  167. Fuhrberg, B.; Hardeland, R.; Poeggela, B.; Behrmann, G. Dramatic Rises of Melatonin and 5-methoxytryptamine in Gonyaulax Exposed to Decreased Temperature. Biol. Rhythm Res. 1997, 28, 144–150. [Google Scholar] [CrossRef]
  168. Cedikova, M.; Pitule, P.; Kripnerova, M.; Markov, M.; Kuncova, J. Multiple Roles of Mitochondria in Aging Processes. Physiol. Res. 2016, 65, S519–S531. [Google Scholar] [PubMed]
  169. Stefonates, R.; Sanz, A. The Role of Mitochondrial ROS in the Aging Brain. FEBS Lett. 2017, in press. [Google Scholar] [CrossRef] [PubMed]
  170. Harman, D. Aging: A Theory Based on Free Radical and Radiation Chemistry. J. Gerontol. 1956, 11, 298–300. [Google Scholar] [CrossRef] [PubMed]
  171. Meng, J.; Lv, Z.; Qiao, X.; Li, X.; Li, Y.; Zhang, Y.; Chen, C. The Decay of Redox-stress Response Capacity is a Substantive Characteristic of Aging: Revising the Redox Theory of Aging. Redox Biol. 2017, 11, 365–374. [Google Scholar] [CrossRef] [PubMed]
  172. Mock, J.T.; Chaudhari, K.; Sidhu, A.; Sumien, N. The Influence of Vitamins E and C and Exercise in Brain Aging. Exp. Gerontol. 2017, 94, 69–72. [Google Scholar] [CrossRef] [PubMed]
  173. Prasad, K.N.; Wu, M.; Bondy, S.C. Telomere Shortening during Aging: Attenuation by Antioxidants and Anti-inflammatory Agents. Mech. Ageing Dev. 2017, 164, 61–66. [Google Scholar] [CrossRef] [PubMed]
  174. Ramis, M.R.; Estaban, S.; Miralles, A.; Tan, D.X.; Reiter, R.J. Protective Effects of Melatonin and Mitochondrial-targeted Antioxidants against Oxidative Stress: A Review. Curr. Med. Chem. 2015, 22, 2690–2711. [Google Scholar] [CrossRef] [PubMed]
  175. Silva, F.S.; Simoes, R.F.; Canto, R.; Oliveira, P.J. Targeting Mitochondria in Cardiovascular Diseases. Curr. Pharm. Res. 2016, 22, 5698–5717. [Google Scholar] [CrossRef]
  176. Prauchner, C.A. Oxidative Stress in Sepsis: Pathophysiological Implications Justifying Antioxidant Co-therapy. Burns 2016, 43, 471–485. [Google Scholar] [CrossRef] [PubMed]
  177. Reiter, R.J.; Tan, D.X.; Poeggeler, B.; Menendez-Pelaez, A.; Chen, L.D.; Saarda, S. Melatonin as a Free Radical Scavenger: Implications for Aging and Age-related Diseases. Ann. N. Y. Acad. Sci. 1994, 719, 1–12. [Google Scholar] [CrossRef] [PubMed]
  178. Poeggeler, B. Melatonin, Aging, and Age-related Diseases: Perspectives for Prevention, Intervention, and Therapy. Endocrine 2005, 27, 201–212. [Google Scholar] [CrossRef]
  179. Reiter, R.J.; Tan, D.X.; Kim, S.J.; Manchester, L.C.; Qi, W.; Garcia, J.J.; Cabrera, J.C.; El-Sokkary, G.; Rouvier-Garay, V. Augmentation of Indices of Oxidative Damage in Life-long Melatonin-deficient Rats. Mech. Ageing Dev. 1999, 110, 157–173. [Google Scholar] [CrossRef]
  180. Vriend, J.; Reiter, R.J. Melatonin Feedback on Clock Genes: A Theory Involving the Proteasome. J. Pineal Res. 2015, 58, 1–11. [Google Scholar] [CrossRef] [PubMed]
  181. Cornelissen, G.; Otsuka, K. Chronobiology of Ageing: A Mini-review. Gerontology 2017, 63, 118–128. [Google Scholar] [CrossRef] [PubMed]
  182. Sohal, R.S.; Allen, R.G. Oxidative Stress as a Causal Factor in Differentiation and Aging: A Unifying Hypothesis. Exp. Gerontol. 1990, 25, 499–522. [Google Scholar] [CrossRef]
  183. Reiter, R.J.; Rosales-Corral, S.A.; Tan, D.X.; Alatorre-Jimenez, M.; Lopez, C. Circadian Dysregulation and Melatonin Suppression in the Context of Aging. In Circadian Rhythms and Their Impact on Aging; Jazwenski, M., Belancio, V.P., Hill, S.M., Eds.; Springer: New York, NY, USA, 2017; pp. 1–25. [Google Scholar]
  184. Manella, G.; Asher, G. The Circadian Nature of Mitochondrial Biology. Front. Endocrinol. 2016, 7, 162. [Google Scholar] [CrossRef] [PubMed]
  185. Bratic, A.; Larsson, N.G. The Role of Mitochondria in Aging. J. Clin. Investig. 2013, 123, 951–957. [Google Scholar] [CrossRef] [PubMed]
  186. Koltover, V.K. Free Radical Timer of Aging: From Chemistry of Free Radicals to Systems Theory of Reliability. Curr. Aging Sci. 2017, 10, 12–17. [Google Scholar] [CrossRef] [PubMed]
  187. Lopez, A.; Ortiz, F.; Doerrier, C.; Venegas, C.; Fernandez-Ortiz, M.; Aranda, P.; Diaz-Casado, M.E.; Fernandez-Gil, B.; Barriocanal-Casado, E.; Escames, G.; et al. Mitochondrial Impairment and Melatonin Protection in Parkinsonian Mice Do Not Depend on Inducible or Nitric Oxide Syntheses. PLoS ONE 2017, 12, e0183090. [Google Scholar] [CrossRef] [PubMed]
  188. Pi, H.; Xu, S.; Reiter, R.J.; Guo, P.; Zhang, L.; Li, M.; Cao, Z.; Tian, L.; Xie, J.; Zhang, R.; et al. SIRT3-SOD2-mROS-dependent Autophagy in Cadmium-induced Hepatotoxicity and Salvage by Melatonin. Autophagy 2015, 11, 1037–1051. [Google Scholar] [CrossRef] [PubMed]
  189. Zhou, H.; Du, W.; Li, Y.; Shi, C.; Hu, N.; Ma, S.; Wang, W.; Ren, J. Effects of Melatonin on Fatty Liver Disease: The Role of NR4A1/DNA-RKcs/p53 Pathway, Mitochondrial Fission, and Mitophagy. J. Pineal Res. 2017, 63, e12490. [Google Scholar] [CrossRef] [PubMed]
  190. Slominski, A.; Zmijewski, M.A.; Semak, I.; Kim, T.K.; Janjetovic, Z.; Slominski, R.M.; Zmijewski, J.W. Melatonin, Mitochondria, and the Skin. Cell. Mol. Life Sci. 2017, 74, 3913–3926. [Google Scholar] [CrossRef] [PubMed]
  191. Baltatu, O.C.; Amaral, F.G.; Campos, L.A.; Cipolla-Neto, J. Melatonin, Mitochondria and Hypertension. Cell. Mol. Life Sci. 2017, 74, 3955–3964. [Google Scholar] [CrossRef] [PubMed]
  192. Wongprayoon, P.; Govitrapong, P. Melatonin as a Mitochondrial Protector in Neurodegenerative Diseases. Cell. Mol. Life Sci. 2017, 74, 3999–4014. [Google Scholar] [CrossRef] [PubMed]
  193. Benot, S.; Goberna, R.; Reiter, R.J.; Garcia-Maurino, S.; Osuna, C.; Guerrero, J.M. Physiological levels of Melatonin Contribute to the Antioxidant Capacity of Human Serum. J. Pineal Res. 1999, 27, 59–64. [Google Scholar] [CrossRef] [PubMed]
  194. Reiter, R.J.; Richardson, B.A.; Johnson, L.Y.; Ferguson, B.N.; Dink, D.T. Pineal Melatonin Rhythm in Aging Syrian Hamsters. Science 1980, 210, 1372–1373. [Google Scholar] [CrossRef] [PubMed]
  195. Reiter, R.J.; Craft, C.M.; Johnson, J.E., Jr.; King, T.S.; Richardson, B.A.; Vaughan, G.M.; Vaughan, M.K. Age-associated Reduction in Nocturnal Pineal Melatonin Levels in Female Rats. Endocrinology 1981, 109, 1295–1297. [Google Scholar] [CrossRef] [PubMed]
  196. Sanchez-Hidalgo, M.; de la Lastra, C.; Carrascosa-Salmoral, M.P.; Naranjo, M.C.; Gomez-Corvera, A.; Caballero, B.; Guerrero, J.M. Age-related Changes in Melatonin Synthesis in Rat Extrapineal Tissues. Exp. Gerontol. 2009, 44, 328–334. [Google Scholar] [CrossRef] [PubMed]
  197. Pappolla, M.A.; Simovich, M.J.; Bryant-Thomas, T.; Chyan, Y.L.; Poeggeler, B.; Dubocovich, M.; Bick, R.; Perry, G.; Cruz-Sanchez, F.; Smith, M.A. The Neuroprotective Activities of Melatonin against the Alzheimer Beta-protein are Not Mediated by Melatonin Membrane Receptors. J. Pineal Res. 2002, 32, 135–142. [Google Scholar] [CrossRef] [PubMed]
  198. Miller, E.; Morel, A.; Sasco, L.; Saluk, J. Melatonin Redox Activity: Its Potential Clinical Applications in Neurodegenerative Disorders. Curr. Top. Med. Chem. 2015, 15, 163–169. [Google Scholar] [CrossRef] [PubMed]
  199. Shukla, M.; Govitrapong, P.; Boontem, P.; Reiter, R.J.; Satayavivad, J. Mechanisms of Melatonin in Alleviating Alzheimer’s Disease. Curr. Neuropharmacol. 2017, 15, 1010–1031. [Google Scholar] [CrossRef] [PubMed]
  200. Milani, M.; Sparavigna, A. Antiaging Efficacy of Melatonin-based Day and Night Creams: A Randomized Split Face, Assessor-blinded Proof-of-concept Trial. Clin. Cosmet. Investig. Dermatol. 2018, 11, 51–57. [Google Scholar] [CrossRef] [PubMed]
  201. Tamura, H.; Kawamoto, M.; Sato, S.; Tamura, I.; Maekawa, R.; Taketani, T.; Aasada, H.; Takaki, E.; Nakai, A.; Reiter, R.J.; et al. Long-term Melatonin Treatment Delays Ovarian Aging. J. Pineal Res. 2017, 62, e12381. [Google Scholar] [CrossRef] [PubMed]
  202. Cardinali, D.P.; Vigo, D.E.; Olivar, N.; Vidal, M.F.; Furio, A.M.; Brusco, L.I. Therapeutic Application of Melatonin in Mild Cognitive Impairment. Am. J. Neurogener. Dis. 2012, 1, 280–291. [Google Scholar]
  203. Boyko, Y.; Jennum, P.; Toft, P. Sleep Quality and Circadian Rhythm Disruption in the Intensive Care Unit: A Review. Nat. Sci. Sleep 2017, 9, 277–284. [Google Scholar] [CrossRef] [PubMed]
  204. Sanchez-Barcelo, E.J.; Rueda, N.; Mediavilla, M.D.; Martinez-Cue, C.; Reiter, R.J. Clinical Uses of Melatonin in Neurological Diseases and Mental Behavioral Disorders. Curr. Med. Chem. 2017, 24, 1–28. [Google Scholar] [CrossRef] [PubMed]
  205. Alvarez-Sanchez, N.; Cruz-Chamorro, I.; Diaz-Sanchez, M.; Sarmiento-Soto, H.; Medrano-Campillo, P.; Martinez-Lopez, A.; Lardone, P.J.; Guerrero, J.M.; Carrillo-Vico, A. Melatonin Reduces Inflammatory Response in Peripheral T Helper Lymphocytes from Relapsing-remitting Multiple Sclerosis Patients. J. Pineal Res. 2017, 63, e12442. [Google Scholar] [CrossRef] [PubMed]
  206. Lopez-Gonzalez, A.; Alvarez-Sanchez, N.; Lardone, R.J.; Cruz-Chamorro, L.; Martinez-Lopez, A.; Guerrero, J.M.; Reiter, R.J.; Carrillo-Vico, A. Melatonin Treatment Improves Primary Progressive Multiple Sclerosis: A Case Report. J. Pineal Res. 2015, 58, 173–177. [Google Scholar] [CrossRef] [PubMed]
  207. Leon, J.; Acuna-Castroviejo, D.; Sainz, R.M.; Mayo, J.C.; Tan, D.X.; Reiter, R.J. Melatonin and Mitochondrial Function. Life Sci. 2004, 1, 765–790. [Google Scholar] [CrossRef] [PubMed]
  208. Paradies, G.; Petrosillo, G.; Paradies, V.; Reiter, R.J.; Ruggiero, F.M. Melatonin, Cardiolipin and Mitochondrial Bioenergetics in Health and Disease. J Pineal Res 2010, 48, 297–310. [Google Scholar] [CrossRef] [PubMed]
  209. Paradies, G.; Paradies, V.; Ruggiero, F.M.; Petrosillo, G. Protective Role of Melatonin in Mitochondrial Function and Related Disorders. Arch. Toxicol. 2015, 89, 923–929. [Google Scholar] [CrossRef] [PubMed]
  210. Paradies, G.; Paradies, V.; Ruggiero, F.M.; Petrosillo, G. Changes in the Mitochondrial Permeability Transition Pore in Aging and Age-associated Diseases. Mech. Ageing Dev. 2013, 134, 1–9. [Google Scholar] [CrossRef] [PubMed]
  211. Wang, P.; Sun, X.; Xie, Y.; Li, M.; Chen, W.; Zhang, S.; Liang, D.; Ma, F. Melatonin Regulates Proteomic Changes during Leaf Senescence in Malus hupehensis. J. Pineal Res. 2014, 57, 291–307. [Google Scholar] [CrossRef] [PubMed]
  212. Liang, C.; Zheng, G.; Li, W.; Wang, Y.; Hu, B.; Wang, H.; Wu, H.; Qian, Y.; Zhu, X.G.; Tan, D.X.; Chen, S.Y.; Chu, C. Melatonin Delays Leaf Senescence and Enhances Salt Stress Tolerance in Rice. J. Pineal Res. 2015, 59, 91–101. [Google Scholar] [CrossRef] [PubMed]
  213. Gomez-Cabrera, M.C.; Ristow, M.; Vina, J. Antioxidant Supplements in Exercise: Worse Than Useless? Am. J. Physiol. Endocrinol. Metab. 2012, 302, E476–E477. [Google Scholar] [CrossRef] [PubMed]
  214. Soysal, P.; Isik, A.T.; Carvalho, A.F.; Fernandes, B.S.; Solmi, M.; Schofield, P.; Veronese, N.; Stubbs, B. Oxidative Stress and Frailty: A Systemic Review and Synthesis of the Best Evidence. Maturitas 2017, 99, 66–72. [Google Scholar] [CrossRef] [PubMed]
  215. Meng, X.; Li, Y.; Zhou, Y.; Gan, R.Y.; Xu, D.P.; Li, H.B. Dietary Sources and Bioactivities of Melatonin. Nutrients 2017, 9, E367. [Google Scholar] [CrossRef] [PubMed]
  216. Liochev, S.I. Which is the Most Significant Cause of Aging? Antioxidants 2015, 17, 793–810. [Google Scholar] [CrossRef] [PubMed]
  217. Goodwin, P.J.; Thompson, A.M.; Stambolic, V. Diabetes, Metformin and Breast Cancer. J. Clin. Oncol. 2012, 30, 2812–2814. [Google Scholar] [CrossRef] [PubMed]
  218. Leone, A.; Di Gennaro, E.; Bruzzese, F.; Avallone, A.; Budillon, A. New Perspective for an Old Antidiabetic Drug: Metformin as Anticancer Agent. Cancer Treat. Res. 2014, 159, 355–376. [Google Scholar] [PubMed]
  219. Barzilai, N.; Crandall, J.P.; Kritcherisky, S.B.; Espeland, M.A. Metformin as a Tool to Target Ageing. Cell Metab. 2016, 119, 662–665. [Google Scholar]
  220. Kurhaluk, N.; Bojkova, B.; Radkowski, M.; Zaitseva, O.V.; Kyrüenko, S.; Demkow, U.; Winklewski, P.J. Melatonin and Metformin Diminish Oxidative Stress in Heart Tissue in a Rat Model of High Fat Diet and Mammary Carcinogenesis. Arch. Exp. Med. Biol. 2017, 128. in press. [Google Scholar]
  221. Asghari, A.; Akbari, G.; Meghdadi, A.; Mortazavi, P. Effects of Melatonin and Metformin Co-administration on Testicular Ischemia/Reperfusion Injury in Rats. J. Pediatr. Urol. 2016, 12, 410.e1–410.e7. [Google Scholar] [CrossRef] [PubMed]
Figure 1. The chemical reduction or the addition of energy to ground state oxygen generates products referred to as reactive oxygen species (ROS). The most reactive of these derivatives are peroxynitrite and the hydroxyl radical. The conversion of hydrogen peroxide to the hydroxyl radical requires a transition metal with the conversion usually being referred to as the Fenton reaction. The red asterisk (*) identifies products that have been reported to be directly scavenged by melatonin and its metabolites. The evidence of these scavenging reactions is much stronger for some ROS than for others. Melatonin also stimulates antioxidant enzymes, e.g., superoxide dismutases (SOD), glutathione peroxidases (GPx), and glutathione reductase (GRd) to indirectly remove toxic ROS. The most toxic species, i.e., peroxynitrite and the hydroxyl radical, are not enzymatically degraded; they can only be removed by a direct scavenger. CAT = catalase.
Figure 1. The chemical reduction or the addition of energy to ground state oxygen generates products referred to as reactive oxygen species (ROS). The most reactive of these derivatives are peroxynitrite and the hydroxyl radical. The conversion of hydrogen peroxide to the hydroxyl radical requires a transition metal with the conversion usually being referred to as the Fenton reaction. The red asterisk (*) identifies products that have been reported to be directly scavenged by melatonin and its metabolites. The evidence of these scavenging reactions is much stronger for some ROS than for others. Melatonin also stimulates antioxidant enzymes, e.g., superoxide dismutases (SOD), glutathione peroxidases (GPx), and glutathione reductase (GRd) to indirectly remove toxic ROS. The most toxic species, i.e., peroxynitrite and the hydroxyl radical, are not enzymatically degraded; they can only be removed by a direct scavenger. CAT = catalase.
Molecules 23 00509 g001
Figure 2. This figure illustrates the structure of a mitochondrion and the location of the complexes (CI-CV) that constitute the electron transport chain that engages in oxidative phosphorylation, which results in the generation of energy in the form of ATP. Free radicals are formed when electrons leak and reduce nearby oxygen (O2) molecules to form the superoxide anion radical (O2). CI releases electrons into the mitochondrial matrix, while CIII releases them into both the matrix and the intramembrane space. Once formed, the O2 can be dismutated by superoxide dismutase (SOD) to hydrogen peroxide (H2O2) with its eventual conversion to the hydroxyl radical (•OH). O2 can also couple with nitric oxide (NO•) to produce the peroxynitrite anion (ONOO). Since melatonin is both taken up and synthesized in mitochondria, it is in an optimal position to scavenge these toxic species.
Figure 2. This figure illustrates the structure of a mitochondrion and the location of the complexes (CI-CV) that constitute the electron transport chain that engages in oxidative phosphorylation, which results in the generation of energy in the form of ATP. Free radicals are formed when electrons leak and reduce nearby oxygen (O2) molecules to form the superoxide anion radical (O2). CI releases electrons into the mitochondrial matrix, while CIII releases them into both the matrix and the intramembrane space. Once formed, the O2 can be dismutated by superoxide dismutase (SOD) to hydrogen peroxide (H2O2) with its eventual conversion to the hydroxyl radical (•OH). O2 can also couple with nitric oxide (NO•) to produce the peroxynitrite anion (ONOO). Since melatonin is both taken up and synthesized in mitochondria, it is in an optimal position to scavenge these toxic species.
Molecules 23 00509 g002
Figure 3. The structure of melatonin and some of its metabolites that have been shown to detoxify reactive oxygen and reactive nitrogen species. Additionally, some of these have other actions that enhance their ability to reduce oxidative stress, e.g., chelation of transition metal ions, promotion of antioxidant enzymes, inhibition of pro-oxidant enzymes, reducing electron leaking from the respiratory chain complexes, etc. Also shown is the sequence by which these metabolites are formed. This sequential formation of metabolites from melatonin, along with their ability to scavenge radicals, is referred to as melatonin′s antioxidant cascade.
Figure 3. The structure of melatonin and some of its metabolites that have been shown to detoxify reactive oxygen and reactive nitrogen species. Additionally, some of these have other actions that enhance their ability to reduce oxidative stress, e.g., chelation of transition metal ions, promotion of antioxidant enzymes, inhibition of pro-oxidant enzymes, reducing electron leaking from the respiratory chain complexes, etc. Also shown is the sequence by which these metabolites are formed. This sequential formation of metabolites from melatonin, along with their ability to scavenge radicals, is referred to as melatonin′s antioxidant cascade.
Molecules 23 00509 g003
Figure 4. The oligopeptide transporters, PEPT1/2, have recently been reported to be present in mitochondrial membranes. These transporters are believed to move melatonin into mitochondria against a gradient. This may explain the much higher concentration of melatonin in mitochondria than in other subcellular compartments. Moreover, high melatonin levels in mitochondria would be consistent with the marked ability of this antioxidant to protect these organelles from free radical damage as it occurs during aging and as a result of diseases of aging that have a free radical component.
Figure 4. The oligopeptide transporters, PEPT1/2, have recently been reported to be present in mitochondrial membranes. These transporters are believed to move melatonin into mitochondria against a gradient. This may explain the much higher concentration of melatonin in mitochondria than in other subcellular compartments. Moreover, high melatonin levels in mitochondria would be consistent with the marked ability of this antioxidant to protect these organelles from free radical damage as it occurs during aging and as a result of diseases of aging that have a free radical component.
Molecules 23 00509 g004
Figure 5. This is an illustration of what is referred to as the endosymbiotic theory for the origin of mitochondria (and chloroplasts) and why these organelles in present-day eukaryotes likely have the ability to produce melatonin. A couple of billion years ago, prokaryotes phagocytized proteobacteria, which are known to synthesize melatonin; these bacteria were initially digested and used as nutrition. During evolution, the ingested bacteria eventually developed a mutually-beneficial symbiotic relationship with the cells that ingested them and they evolved into mitochondria. When they did so, the evolved mitochondria retained the ability to produce melatonin (brown image). As a result, present-day eukaryotic cells synthesize melatonin as shown in several reports cited in the current review. Likewise, some of the same prokaryotes also engulfed photosynthetic, melatonin-producing bacteria which evolved into chloroplasts of plant cells (green image); chloroplasts also have been shown to be involved in melatonin synthesis. Since plant cells have both chloroplasts and mitochondria may explain why plants generally have higher cellular concentrations of melatonin than do animal cells, which only have mitochondria.
Figure 5. This is an illustration of what is referred to as the endosymbiotic theory for the origin of mitochondria (and chloroplasts) and why these organelles in present-day eukaryotes likely have the ability to produce melatonin. A couple of billion years ago, prokaryotes phagocytized proteobacteria, which are known to synthesize melatonin; these bacteria were initially digested and used as nutrition. During evolution, the ingested bacteria eventually developed a mutually-beneficial symbiotic relationship with the cells that ingested them and they evolved into mitochondria. When they did so, the evolved mitochondria retained the ability to produce melatonin (brown image). As a result, present-day eukaryotic cells synthesize melatonin as shown in several reports cited in the current review. Likewise, some of the same prokaryotes also engulfed photosynthetic, melatonin-producing bacteria which evolved into chloroplasts of plant cells (green image); chloroplasts also have been shown to be involved in melatonin synthesis. Since plant cells have both chloroplasts and mitochondria may explain why plants generally have higher cellular concentrations of melatonin than do animal cells, which only have mitochondria.
Molecules 23 00509 g005
Figure 6. This figure is a flow diagram that links free radicals and the associated oxidative damage with the progression of the aging phenotype and the onset and development of age-related diseases. The cloud at the top lists many of the iterations of the free radical theory of aging that have been introduced over the last 60 years. In the current review, we discuss the evidence that melatonin could be relevant to the processes summarized. ROS = Reactive oxygen species; AD = Alzheimer disease; PD = Parkinson disease; HD = Huntington disease; MS = Multiple sclerosis; ALS = amyotrophic lateral sclerosis.
Figure 6. This figure is a flow diagram that links free radicals and the associated oxidative damage with the progression of the aging phenotype and the onset and development of age-related diseases. The cloud at the top lists many of the iterations of the free radical theory of aging that have been introduced over the last 60 years. In the current review, we discuss the evidence that melatonin could be relevant to the processes summarized. ROS = Reactive oxygen species; AD = Alzheimer disease; PD = Parkinson disease; HD = Huntington disease; MS = Multiple sclerosis; ALS = amyotrophic lateral sclerosis.
Molecules 23 00509 g006

Share and Cite

MDPI and ACS Style

Reiter, R.J.; Tan, D.X.; Rosales-Corral, S.; Galano, A.; Zhou, X.J.; Xu, B. Mitochondria: Central Organelles for Melatonin′s Antioxidant and Anti-Aging Actions. Molecules 2018, 23, 509.

AMA Style

Reiter RJ, Tan DX, Rosales-Corral S, Galano A, Zhou XJ, Xu B. Mitochondria: Central Organelles for Melatonin′s Antioxidant and Anti-Aging Actions. Molecules. 2018; 23(2):509.

Chicago/Turabian Style

Reiter, Russel J., Dun Xian Tan, Sergio Rosales-Corral, Annia Galano, Xin Jia Zhou, and Bing Xu. 2018. "Mitochondria: Central Organelles for Melatonin′s Antioxidant and Anti-Aging Actions" Molecules 23, no. 2: 509.

Article Metrics

Back to TopTop