Next Article in Journal
Biomechanical Analysis of Latin Dancers’ Lower Limb during Normal Walking
Next Article in Special Issue
Biocompatibility and Transplantation Efficacy of the C-Clear Artificial Cornea in a Rabbit Chemical Burn Model
Previous Article in Journal
Whole Liver Derived Acellular Extracellular Matrix for Bioengineering of Liver Constructs: An Updated Review
 
 
Search for Articles:
Title / Keyword
Author / Affiliation / Email
Journal
Article Type
 
 
Advanced Search
 
Section
Special Issue
Volume
Issue
Number
Page
 
Journals
Bioengineering
Volume 10
Issue 10
10.3390/bioengineering10101127
bioengineering-logo
Submit to this Journal Review for this Journal Propose a Special Issue
► Article Menu

Article Menu

share Share announcement Help format_quote Cite question_answer Discuss in SciProfiles thumb_up
...
Endorse textsms
...
Comment
first_page
settings
Order Article Reprints
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Review

Quercetin and Related Analogs as Therapeutics to Promote Tissue Repair

by
Tina B. McKay
1,
Kyle A. Emmitte
2,
Carrie German
3 and
Dimitrios Karamichos
2,4,5,*
1
Department of Anesthesia, Critical Care and Pain Medicine, Massachusetts General Hospital, Boston, MA 02114, USA
2
Department of Pharmaceutical Sciences, UNT System College of Pharmacy, University of North Texas Health Science Center, Fort Worth, TX 76107, USA
3
CFD Research Corporation, Computational Biology Division, Huntsville, AL 35806, USA
4
North Texas Eye Research Institute, University of North Texas Health Science Center, Fort Worth, TX 76107, USA
5
Department of Pharmacology and Neuroscience, School of Biomedical Sciences, University of North Texas Health Science Center, Fort Worth, TX 76107, USA
*
Author to whom correspondence should be addressed.
Bioengineering 2023, 10(10), 1127; https://doi.org/10.3390/bioengineering10101127
Submission received: 22 August 2023 / Revised: 11 September 2023 / Accepted: 21 September 2023 / Published: 25 September 2023
(This article belongs to the Special Issue Bioengineering and the Eye, Volume II)
Browse Figures
Versions Notes

Abstract

:
Quercetin is a polyphenol of the flavonoid class of secondary metabolites that is widely distributed in the plant kingdom. Quercetin has been found to exhibit potent bioactivity in the areas of wound healing, neuroprotection, and anti-aging research. Naturally found in highly glycosylated forms, aglycone quercetin has low solubility in aqueous environments, which has heavily limited its clinical applications. To improve the stability and bioavailability of quercetin, efforts have been made to chemically modify quercetin and related flavonoids so as to improve aqueous solubility while retaining bioactivity. In this review, we provide an updated overview of the biological properties of quercetin and proposed mechanisms of actions in the context of wound healing and aging. We also provide a description of recent developments in synthetic approaches to improve the solubility and stability of quercetin and related analogs for therapeutic applications. Further research in these areas is expected to enable translational applications to improve ocular wound healing and tissue repair.

Graphical Abstract

1. Introduction

The earliest evidence for the use of medicinal plants in archaic human history dates back to the Paleolithic period by the Neanderthals nearly 60,000 years ago [1,2,3]. In modern times, natural products and their modified semisynthetic forms remain a steady source of new therapeutics to treat disease, and about one-quarter of natural products approved by the Food and Drug Administration in the United States are plant-derived [4,5]. Quercetin (3,5,7,3′,4′-pentahydroxyflavone) is a polyphenol flavonoid derived from plants and legumes that exhibits a diverse range of bioactivity. Originally derived from the Latin word quercetum, meaning oak-wood [6], quercetin is a small molecule with a distinctive yellow color that possesses potent antioxidant properties as a reactive oxygen species (ROS) scavenger. Quercetin and other flavonoids are abundant in apples, grapes, plums, coriander, corn poppy, and fennel, and enriched in the leaves of onion, thale cress, olives, and sweet potatoes, among other fruits and vegetables [7,8,9]. Quercetin content in onion leaves is estimated at ~1500 mg/kg dry weight of plant material [8]. The biosynthetic pathways involved in flavonoid synthesis have been extensively reviewed in the literature [10,11,12]. Following exposure to ultraviolet light (UV)-B, quercetin levels significantly increase in the leaves of C. sativum (coriander) and other plants, and its production, in concert with various polyphenols, is thought to serve a functional role against ROS-induced damage promoted by UV activation [13,14]. This adaptive dose-dependent response, termed hormesis, has been proposed as a protective mechanism present in plants that involves increased release of flavonoids in response to exogenous stressors that may contribute to enhanced resilience to further high-dose cytotoxins [15]. The beneficial properties of quercetin and related flavonoids is largely conserved in the animal kingdom and thought to be a form of ‘xenohormesis,’ in which protective agents derived from one domain (plants) are beneficial to another organism (humans) via shared survival mechanisms but independent biological pathways [16].
Perhaps the most well-studied therapeutic property of quercetin is direct quenching of ROS to a less reactive chemical species, as well as chelation of exogenous reactive metals that may also promote the generation of excess ROS [17,18]. Recent work has highlighted other downstream pathways modulated by quercetin, including activation of the sirtuin family of proteins [19]. Sirtuins are deacetylases that regulate regenerative responses in the cell and are activated by exogenous stressors, such as extreme cold, hypoxia, and nutrition restriction [20,21,22]. Quercetin supplementation has been associated with activation of these pro-reparative pathways and favorable neuroprotective and anti-aging properties in animal models [23,24]. Quercetin is also a phytoestrogen, a known agonist of estrogen receptor α and β, by which it may also influence downstream hormonally-regulated pathways involved in cell proliferation [25].
Due to its potent biological properties, further developments to improve the bioavailability of quercetin and related analogs have gained substantial interest in recent years. In this review article, we provide an updated overview of the biological properties of quercetin in the context of wound healing with a focus on ocular applications; we also discuss current approaches to improve bioavailability via chemical modification. Further study of quercetin and related analogs is expected to accelerate therapeutic applications and enable broad utilization of these natural products to improve human health.

2. Bioactivity

Many of the health benefits associated with consuming green leafy plants have been at least partly attributed to the presence and bioactivity of quercetin and related flavonoids [26,27,28]. As anecdotal evidence, onion extract has long been proposed as a natural treatment for scarring and burns [29,30], and onions are known to be composed of moderate amounts of quercetin that can be absorbed into the bloodstream following oral consumption [31,32]. Oral bioavailability of quercetin via food derivatives occurs with a blood distribution of 0–0.44 μM/L in the plasma of 3′-methyl quercetin following a single intake of ~1 L of apple cider [33]. While high-dose intake of quercetin is thought to be generally safe, the therapeutic effectiveness of quercetin administered orally is largely limited by its low bioavailability [34]. Quercetin is highly glycosylated in its natural form with reduced absorption as an aglycone. Structural and functional analyses of quercetin have shown a relationship between hydroxylation of quercetin at C3, C5, C7, C3′, and C4′ and increased antioxidant capabilities [35]. Preclinical studies in animal models have suggested that quercetin has potent antifibrotic, antioxidative, and anti-inflammatory properties in the anterior segment of the eye that favors tissue repair and maintenance (Table 1). In this section, we review the biological effects of quercetin in the context of wound healing and aging with a focus on ocular implications.

2.1. Wound Healing

Preclinical studies have revealed promising results suggesting that quercetin treatment may inhibit fibrosis in different tissues. We have found that topical application of quercetin to the corneal surface appears to lead to a moderate reduction in scarification in mice and rabbits following epithelial debridement and penetrating keratectomy, respectively [36]. Studies in the skin have shown similar findings with less scarring observed with quercetin application following burn exposure or wounding [41,42], which has also been proposed as a potential preventative treatment for the formation of keloids [43]. In diabetic animal models that are commonly associated with decreased wound healing capabilities, application of quercetin has shown improved skin closure following laceration and chronic wound management [44,45]. The antioxidative properties of quercetin also appear to extend to protection against diabetes-associated cataract formation in animal models of type I diabetes [37,38]. Moreover, topical ocular application of quercetin and resveratrol have been associated with decreased proinflammatory cytokine tear secretion and improved ocular manifestations in mouse models of dry eye disease [39,40], suggesting that quercetin may also influence inflammatory processes that affect the ocular surface.
In terms of the mechanisms underlying the observed antifibrotic properties, quercetin has been found to be a potent metabolic regulator at both the individual cell level [46] and the tissue level in the liver [47], leading to systemic effects on glucose and lipid distributions [48]. Studies in the lung have identified increased lactate production, lower pH in the extracellular space, and myofibroblast differentiation in fibrotic tissue [49,50], and this process may be collectively inhibited by quercetin treatment via modulation of the redox component [51,52]. We have found that quercetin stimulation reduces lactate production and expression of α-smooth muscle actin (α-SMA) and collagen type III in human corneal fibroblasts cultured in vitro [53]. Altered metabolite levels and energy metabolism via the tricarboxylic acid cycle has been observed in corneal fibroblasts derived from patients with keratoconus [54], a corneal thinning disease associated with altered extracellular matrix deposition in the corneal stroma, and quercetin treatment has been found to influence this metabolic phenotype in concert with decreased expression of fibrotic markers [53,55]. The metabolic effects of quercetin extend to cancer cell types, with a similar reduction in lactate production observed with quercetin treatment [56], and is thought to inhibit the Warburg metabolic phenotype [57]. The Warburg effect is a metabolic change in which energy production via aerobic glycolysis is favored over the high-demand tricarboxylic acid cycle, which can be cumbersome in highly proliferative cell states, such as cancer [58].
The biological activity of quercetin has also been attributed to regulation of the acute immune response involving macrophages in the wounded area, whereby modulation of the proinflammatory response appears to ameliorate tissue damage that may be promoted by excessive ROS production by invading immune cells [44]. Quercetin has also been found to reduce expression of proinflammatory cytokines directly, including tumor necrosis factor-α (TNF-α), interleukin (IL)-1β, and IL-6 in concert with increased canonical Wnt-signaling in the skin of wounded mice treated with quercetin [59]. While the immune response is essential in preventing infection, targeted and controlled regulation of inflammation by small molecules, such as quercetin, may inhibit scar formation in a similar process to anti-inflammatory treatments [60]. Moreover, the antioxidative properties of quercetin extend to its upregulation of protective enzymes responsible for quenching ROS, including superoxide dismutase (SOD) 1 and 2 and catalase in an atopic dermatitis model [61]. Quercetin has also been reported as an inhibitor of angiogenesis via regulation of the vascular endothelial growth factor pathway in retinal models [62,63]. While these preclinical studies have highlighted the broad biological activity of quercetin, double-blinded placebo-controlled studies in human populations are still needed to establish the therapeutic benefits of quercetin application in ocular wound healing.

2.2. Aging

The biological markers of aging are highly conserved throughout the animal kingdom from yeast to humans. Changes associated with aging include deficiencies in genomic stability, telomere length, nutritional sensing, and mitochondrial function, among others [64] that collectively determine cell, tissue, and organismal survival. Downstream effectors influenced by quercetin treatment include its ROS-scavenging properties and mediators of autophagy, among other pathways (Figure 1). As a potent antioxidant, quercetin may inhibit ROS-driven processes that are associated with DNA damage, activation of the inhibitor of the NF-κB kinase (IKK) signaling pathway, induction of protein modifications and proteasomal degradation, and tumor necrosis factor-receptor (TNF-R)-induced apoptosis. The pleiotropic properties of quercetin include its potent antioxidative properties, as well as its functional effects on sirtuin signaling and mitochondrial function mediated via activation of 5′-adenosine monophosphate-activated protein kinase (AMPK). Moreover, many of the biological effects of quercetin and resveratrol in terms of aging and longevity have been at least partly attributed to their influence on sirtuin activation [24,65,66]. The sirtuin family of proteins are deacetylases important in DNA repair, nutritional responses, and cell metabolism. Sirtuin 1 is an isoform associated with histone deacetylation that is particularly important in mitochondrial biogenesis, and inhibition of Sirtuin 1 via chemical blocking leads to widespread increases in the acetylation patterns of proteins predominately found within the mitochondria, thus highlighting its important role in mitochondrial function [67]. Sirtuin 1 is an activator of peroxisome proliferator-activated receptor γ coactivator-1α (PGC-1α), which is also responsive to exercise and nutrition [68]. Quercetin has been found to promote a 5-fold increase in Sirtuin 1 activity in yeast [24], with up to a 60% increase in lifespan observed [69].
In terms of other pathways influenced by quercetin, activation of estrogen receptor β and the estrogen response element by quercetin stimulation appear to be comparable or even higher than estradiol in vitro, which may influence cell proliferation [25,70]. While the hormonal properties of quercetin as a phytoestrogen have focused heavily on cancer cell types, the wound healing properties of quercetin observed in the epidermis and corneal stroma may also be related to its activation of estrogen receptor–mediated signaling. Further mechanistic studies of quercetin and related analogs may aid in identifying the prime molecular targets involved in its antifibrotic properties and enable more targeted therapeutic development.
Bioengineering 10 01127 g001
Figure 1. Selected downstream signaling pathways important in the bioactivity of quercetin. (A) Antioxidative properties of quercetin may influence downstream signaling pathways mediated by reactive oxygen species (ROS). (B) Quercetin may influence mitochondrial function via activation of Sirtuin 1 and mitochondrial-associated genes. (C) As a phytoestrogen, quercetin is able to bind to membrane-bound estrogen receptors or cytosolic estrogen receptor α or β and influence downstream signaling. (Abbreviations: protein kinase B (AKT); 5′-adenosine monophosphate–activated protein kinase (AMPK); estrogen receptor (ER)α/β; endoplasmic reticulum associated protein degradation (ERAD); estrogen response element (ERE); inhibitor of NF-κB kinase (IKK); nuclear respiratory factor 1 (NRF1); poly (ADP-ribose) polymerase (PARP); peroxisome proliferator–activated receptor-gamma coactivator (PGC1α); transcription factor A mitochondrial (TFAM); and tumor necrosis factor-receptor (TNF-R)). Based on references [71,72,73,74].
Figure 1. Selected downstream signaling pathways important in the bioactivity of quercetin. (A) Antioxidative properties of quercetin may influence downstream signaling pathways mediated by reactive oxygen species (ROS). (B) Quercetin may influence mitochondrial function via activation of Sirtuin 1 and mitochondrial-associated genes. (C) As a phytoestrogen, quercetin is able to bind to membrane-bound estrogen receptors or cytosolic estrogen receptor α or β and influence downstream signaling. (Abbreviations: protein kinase B (AKT); 5′-adenosine monophosphate–activated protein kinase (AMPK); estrogen receptor (ER)α/β; endoplasmic reticulum associated protein degradation (ERAD); estrogen response element (ERE); inhibitor of NF-κB kinase (IKK); nuclear respiratory factor 1 (NRF1); poly (ADP-ribose) polymerase (PARP); peroxisome proliferator–activated receptor-gamma coactivator (PGC1α); transcription factor A mitochondrial (TFAM); and tumor necrosis factor-receptor (TNF-R)). Based on references [71,72,73,74].
Bioengineering 10 01127 g001

3. Therapeutic Development

Flavonoids consist of a chromane ring (A- and C-rings) substituted by a phenyl ring (B-ring) at C2 (Figure 2). Quercetin and structurally similar natural products maintain an unsaturated bond at C2-C3 and a ketone at C4 of the C-ring and are a part of the flavone subclass of flavonoids. Variation between these compounds primarily relates to the number and position of the phenolic hydroxyl groups, which may be methylated in some instances [75]. Each of these compounds is highly aromatic and lacks ionizable functional groups at physiologically relevant pH values, which contributes to their aforementioned low aqueous solubility and bioavailability [34]. Low permeability and metabolic instability are also common liabilities that hinder the therapeutic utility of this class of compounds [75]. To overcome such issues while simultaneously maintaining or enhancing bioactivity, medicinal chemists have modified quercetin and related natural products through the installation of additional functional groups, creating new synthetic flavonoids. In this section, we present some recent examples of the synthetic flavonoid approach that have translated to notable improvements in physiochemical and/or pharmacological advantages relative to the parent natural product. While most of the examples presented here did not arise specifically with wound healing in view, these instances nonetheless demonstrate general approaches to enhancing physiochemical and/or pharmacological properties that may be extended to a variety of therapeutic indications, including wound healing.
One of the more common strategies employed across synthetic flavonoid approaches representing a diverse array of indications and mechanisms of action involves the installation of flexible functional groups containing basic amines (Figure 3) [76,77,78,79,80,81,82,83,84]. Basic amines offer the opportunity to prepare salts, which can aid formulation and solubility in aqueous systems and create additional potential for favorable binding interactions with the pharmacological target(s) that may lead to increased potency. Depending on the chemical nature of the basic amine-containing group, the appendage may also increase lipophilicity relative to the parent compound, which can often improve the permeability of biological membranes.
Wu and coworkers synthesized negletein analog 1 (FZU-02,006), which contains a tertiary amine linked to the C6-oxygen via an ethylene tether [76]. It has been noted that negletein (7-O-methyl baicalein) has higher metabolic stability than baicalein [85]; thus, the methyl ether at C7 was maintained in 1. The aqueous solubility of the HCl salt of 1 exceeded 1 mg/mL and was >25-fold more potent than baicalein and negletein in an assay measuring inhibition of proliferation of HL-60 leukemia cells. Compound 1 dose-dependently induced apoptosis in the same cell line, and mechanistic studies indicated inhibition of AKT-signaling as a potential mechanism of action for its anticancer activity [76]. Yang and coworkers prepared chrysin analog 2, which possessed the same ethylene- linked tertiary amine as 1, albeit at C7 rather than C6 [77]. The C5 hydroxyl and C4 ketone of 2 are proposed to function as a copper(II) chelator, which is thought to be key to its antioxidant and anti-Aβ1-42 aggregation activity. Further bolstering its potential application to Alzheimer’s disease (AD) therapy, compound 2 also functioned as an inhibitor of both acetylcholinesterase (AChE) and butyrylcholinesterase (BChE). While no physiochemical or pharmacokinetic characterization was reported for 2, calculated properties were predictive of efficient blood–brain barrier (BBB) permeability [77].
In search of compounds with antioxidant and neuroprotective effects, Lee and coworkers synthesized 3, a derivative of quercetin 3-O-methyl ether containing another ethylene-linked tertiary amine at C7 [78]. The HCl salt of 3 had more than 4000-fold higher aqueous solubility than quercetin 3-O-methyl ether while maintaining similar antioxidant activity in vitro. Moreover, in the middle cerebral artery occlusion (MCAO) rat model of cerebral ischemia, compound 3 was neuroprotective compared to vehicle as measured by significant reductions in corrected total infarct volume and percent edema [78]. Efforts to discover new compounds for the treatment of colon cancer by Sun and coworkers identified wogonin analog 4 (LZ-207). Compound 4 is another example with a tertiary-amine-containing group at C7; however, in this case an N-methylpiperazine was linked to the C7-oxygen via a saturated 4-carbon chain. A C2′ methyl ether was also present in 4. The solubility of 4 was more than 125-fold higher than wogonin, and it inhibited viability and induced apoptosis in HCT116 colon cancer cells in vitro. Likewise, 4 dose-dependently suppressed nuclear translocation of the NF-κB transcription factor through interactions with upstream signaling pathways. Xenograft studies in nude mice bearing HCT116 tumors and treated with 4 demonstrated dose-dependent tumor growth inhibition [79]. Helgren and coworkers also used the A-ring for installation of an amine-containing group onto the quercetin scaffold; however, in this case the attachment was made via C8, and the analogs mainly consisted of secondary amines linked to aromatic rings via hydrocarbon chains [80]. These quercetin analogs were screened for activity against three drug-resistant malarial strains, and analog 5 was among the most active compounds, demonstrating 41- to 165-fold improved potency relative to quercetin. Despite the introduction of the highly lipophilic 2,4-dichlorophenethyl group, 5 exhibited nearly 4-fold improved aqueous solubility relative to quercetin, presumably due to the presence of the secondary amine [80].
Modification of the flavonoid scaffold as a strategy for improved physiochemical and/or pharmacological properties is not limited to the A-ring. For example, Mukherjee and coworkers prepared analogs of quercetin with polar functional groups on both the A- and B-rings and discovered B-ring-substituted analog 6, which contains an N-methylpiperazine linked to the C3′-oxygen via a saturated 3-carbon chain [81]. These authors utilized a strategy focused on improving LogD7.4, and 6 proved highly permeable in a Caco-2 bidirectional permeability assay with no evidence of efflux. Inhibition of cell proliferation in HCT-116 (human) and CT-26 (murine) colon cancer cells was greatly enhanced with compound 6 compared to quercetin at 96- and 88-fold, respectively. Mechanistic studies indicate that compound 6 induced oxidative stress in the HCT-116 cells and mediated apoptosis through the mitochondrial integrity pathway. Xenograft studies in BALB/c mice bearing CT-26 tumors demonstrated that compound 6 prolonged survival and dose-dependently reduced tumor volume [81]. Likewise, Chen and coworkers targeted C4′ of apigenin for installation of tertiary-amine-containing groups in their efforts to discover new therapeutics for chronic pancreatitis (CP) [82]. Analog 7 (HJC05100) contains a β-hydroxy amine group attached to the C4′-oxygen and methyl ethers at C5 and C7. The HCl salt of 7 demonstrated >38K-fold higher aqueous solubility than apigenin. Likewise, compound 7 enhanced potency in vitro relative to apigenin in a cell proliferation assay of pancreatic stellate cells and decreased fibrosis in an established mouse model of CP [82].
Wang and coworkers utilized a strategy focused on substitution of both the A- and B-rings of wogonin at C8 and C4′, respectively, in search of optimized cyclin-dependent kinase 9 (CDK9) inhibitors for the treatment of cancer [83]. Optimized analog 8 contains an N-methylpiperazine directly attached to C4′, an ether-linked 3,5-dimethyl-1H-pyrazol-4-yl group at C8, and a methyl ether at C7. Intrinsic aqueous solubility of 8 was more than double that of wogonin and more than 30-fold greater in a pH 4.5 buffered solution. Analog 8 demonstrated greater potency versus CDK9 than wogonin, with a superior selectivity profile versus CDK2. Likewise, 8 was a potent inhibitor of cell proliferation in a suite of 14 different tumor cell lines, and xenograft studies in nude mice bearing MV4-11 (leukemia) tumors demonstrated dose-dependent tumor growth inhibition following treatment with 8 without mortality or significant changes in body weight. Finally, use of the interior C-ring for installation of a tertiary-amine-containing group was also recently reported with nobiletin analog 9 [84]. Aqueous solubility of 9 was 280-fold higher than nobiletin in a pH 7.3 buffered solution and was effective at potentiating the effects of the anticancer agent paclitaxel in vitro, appearing to function as an inhibitor of the P-glycoprotein transporter and the PI3K/AKT pathway. Xenograft studies in nude mice bearing paclitaxel-resistant A549/T tumors demonstrated that 9 enhances the anticancer effects of paclitaxel, reducing tumor volumes without negatively affecting body weight [84].
Synthetic flavonoid strategies for improvement in pharmacological and/or physiochemical properties are not limited to the installation of basic amine-containing functional groups. The appendage of sugars to flavonoids through glycosylation has also been employed in multiple cases [86,87,88,89,90]. In fact, some flavonoids are found as O-glycosides in nature [75]; however, these O-glycosidic bonds are not always metabolically stable [88]. While solubility enhancement via installation of polar sugar groups is not surprising, such changes dramatically lower logP to levels considered unfavorable for passive permeation of lipophilic membranes such as the BBB. Still, transporters such as glucose transporter 1 (GLUT1) can sometimes bring such molecules into the brain via active transport [89].
Zhu and coworkers prepared myricetin analog 10 via installation of a disaccharide at C3′ via a glycosidic bond and conversion to a sodium salt [86] (Figure 4). Aqueous solubility of 10 was excellent and more than 7000-fold higher than myricetin. Moreover, stability of 10 in rat plasma and rat liver microsomes was improved relative to myricetin as indicated by its longer half-life and reduced clearance in both systems. Evaluation of 10 in mice using a model of ulcerative colitis demonstrated its efficacy at reducing inflammation [86]. The same research group continued their optimization of disaccharide myricetin analogs in search of new hypoglycemic agents [87]. All disaccharide derivatives prepared and tested in this effort demonstrated α-glucosidase-inhibitory activity, which has relevance for the treatment of hypoglycemia, and 11 demonstrated 3-fold improved activity in vitro relative to myricetin.
Certain kaempferol derivatives glycosylated at C3 inhibit the p90 ribosomal s6 kinases RSK1/2, which has relevance to the treatment of certain types of cancers, including some triple-negative breast cancers. Li and coworkers have pursued carbasugar analogs of kaempferol in which the metabolically liability of the O-glycosidic bond has been eliminated by replacing the ring oxygen with a methylene unit as exemplified in 12 [88]. Carbasugar strategies have been utilized successfully in the design of marketed therapeutics, notably in the case of antiviral carbocyclic nucleoside drugs [89]. In addition to the methylene replacement of the ring oxygen, the carbasugar of 12 contains an n-propyl group as well as two acetate esters, modifications that raise lipophilicity relative to a traditional sugar. An asymmetric synthesis of the carbasugar moiety of 12 was developed beginning with D-(-)-quinic acid. Compound 12 demonstrated 6-fold enhanced potency versus RSK2 and in blocking proliferation of MCF-7 lung cancer cells in vitro compared to an O-glycoside lead. Likewise, 12 demonstrated improved bioavailability and efficacy in a mouse model of metastatic colonization relative to the same lead [88,90].
Antioxidant and neuroprotective effects of quercetin have relevance to the potential treatment of diseases characterized by neuronal injury and/or neurodegeneration. Given its poor aqueous solubility, low bioavailability, metabolic instability, and the fact that it does not readily cross the BBB [91,92,93], Wang and coworkers sought to improve such properties through glycosylation [94]. Desiring to avoid O-glycosides, the authors utilized click chemistry [95] to install glucose moieties at C3′ and C7 via triazole linkers to arrive at 13. Analog 13 was effective at preventing hydrogen-peroxide-induced neurotoxicity in vitro and demonstrated enhanced neuroprotective effects in a rat model of cerebral ischemia (MCAO) compared to those observed with quercetin [93]. Recent studies have identified interactions between cellular prion protein (PrPC) and Aβ oligomers (Aβo) that contribute to the neurotoxicity observed in Alzheimer’s disease (AD). The flavonoid chrysin has been noted to disrupt Aβo-PrPC and thus represents a potential starting point for the design of new AD therapeutics [96]. Matos and coworkers installed a C-glycoside at C8 and a flexible, basic amine-containing group at C4′ to arrive at 14, a compound that exemplifies both strategies for synthetic flavonoids discussed herein. The solubility of 14 was enhanced compared to chrysin, and it dose-dependently disrupted interactions between Aβo-PrPC in HEK cells. The C8 sugar was shown to be a key structure–activity relationship for this activity [96].

4. Future Outlooks

The identification of potential mechanisms of action and strategies to enhance bioavailability while retaining bioactivity through structural modification has substantially increased interest in the use of quercetin and related analogs for ocular wound healing. A substantial number of studies have demonstrated the therapeutic potential of quercetin and related analogs. With the vast majority of this research having been conducted in preclinical cell culture and animal models, questions regarding human efficacy and safety need to be addressed. While pharmacokinetic studies have been performed at the systemic level using dietary and dietary supplement forms of quercetin, there is a need to perform such studies on the enhanced and modified synthetic analogs. Improved bioavailability via encapsulation of quercetin and related flavonoids also remains an area for further research [97]. Determination of the optimal dosage depending on formulation and therapeutic application are still needed. Further, localized pharmacokinetic studies should be explored to better understand concentration and residence time at the site of action. Complementary pharmacodynamic studies could be used to further elucidate the mechanism of action and support targeted delivery through specific structural modifications.
This may prove challenging. Quercetin was acknowledged by the Food and Drug Administration in 2010 as GRAS (Generally Recognized as Safe) for use as a dietary supplement, yet approval for any therapeutic purpose remains unseen. This demonstration will most likely require a concentrated effort in a specific application by a multidisciplinary team.

5. Conclusions

Quercetin and other flavonoids are bioactive compounds that have been found to exhibit therapeutic effects mediated via their antioxidant properties and activation of mitochondrial-associated factors, including AMPK and Sirtuin 1. As a phytoestrogen, quercetin is also known to bind cell-surface-bound and soluble forms of the estrogen receptors, thereby activating downstream signaling pathways, including estrogen response elements. Until recently, the limited solubility of quercetin and related flavonoids in aqueous solutions has blunted their therapeutic use in ocular applications. Strategies centered on the development of semisynthetic flavonoids substituted with groups designed to improve physiochemical and/or pharmacological properties have proven successful in a variety of preclinical settings and remain a growing area of research.

Author Contributions

Conceptualization, T.B.M., K.A.E. and D.K.; methodology, T.B.M., K.A.E. and D.K.; software, T.B.M., K.A.E. and D.K.; validation, T.B.M., K.A.E. and D.K.; formal analysis, T.B.M., K.A.E. and D.K.; investigation, T.B.M., K.A.E. and D.K.; resources, T.B.M., K.A.E. and D.K.; data curation, T.B.M., K.A.E. and D.K.; writing—original draft preparation, T.B.M., K.A.E., C.G. and D.K.; writing—review and editing, T.B.M., K.A.E., C.G. and D.K.; visualization, T.B.M., K.A.E., C.G. and D.K.; supervision, T.B.M., K.A.E., C.G. and D.K.; project administration, T.B.M., K.A.E., C.G. and D.K.; funding acquisition, D.K. All authors have read and agreed to the published version of the manuscript.

Funding

This study was funded by the National Institutes of Health/National Eye Institute grant R01EY028888 (DK).

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

Not applicable.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Solecki, R.S. Shanidar IV, a Neanderthal Flower Burial in Northern Iraq. Science 1975, 190, 880–881. [Google Scholar] [CrossRef]
  2. Weyrich, L.S.; Duchene, S.; Soubrier, J.; Arriola, L.; Llamas, B.; Breen, J.; Morris, A.G.; Alt, K.W.; Caramelli, D.; Dresely, V.; et al. Neanderthal behaviour, diet, and disease inferred from ancient DNA in dental calculus. Nature 2017, 544, 357–361. [Google Scholar] [CrossRef] [PubMed]
  3. Hardy, K.; Buckley, S.; Collins, M.J.; Estalrrich, A.; Brothwell, D.; Copeland, L.; García-Tabernero, A.; García-Vargas, S.; de la Rasilla, M.; Lalueza-Fox, C.; et al. Neanderthal medics? Evidence for food, cooking, and medicinal plants entrapped in dental calculus. Naturwissenschaften 2012, 99, 617–626. [Google Scholar] [CrossRef] [PubMed]
  4. Patridge, E.; Gareiss, P.; Kinch, M.S.; Hoyer, D. An analysis of FDA-approved drugs: Natural products and their derivatives. Drug Discov. Today 2016, 21, 204–207. [Google Scholar] [CrossRef] [PubMed]
  5. Newman, D.J.; Cragg, G.M. Natural Products as Sources of New Drugs over the Nearly Four Decades from 01/1981 to 09/2019. J. Nat. Prod. 2020, 83, 770–803. [Google Scholar] [CrossRef] [PubMed]
  6. Andrews, E.A.; Lewis, C.T. A Latin Dictionary Founded on Andrews’ Edition of Freund’s Latin Dictionary; Clarendon Press: Oxford, UK, 1896. [Google Scholar]
  7. Bhagwat, S.; Haytowitz, D.B.; Holden, J.M. USDA Database for the Flavonoid Content of Selected Foods, Release 3; US Department of Agriculture: Beltsville, MD, USA, 2011; p. 159. [Google Scholar]
  8. Miean, K.H.; Mohamed, S. Flavonoid (myricetin, quercetin, kaempferol, luteolin, and apigenin) content of edible tropical plants. J. Agric. Food Chem. 2001, 49, 3106–3112. [Google Scholar] [CrossRef]
  9. Ojong, P.B.; Njiti, V.; Guo, Z.; Gao, M.; Besong, S.; Barnes, S.L. Variation of flavonoid content among sweetpotato accessions. J. Am. Soc. Hortic. Sci. 2008, 133, 819–824. [Google Scholar] [CrossRef]
  10. Koes, R.E.; Quattrocchio, F.; Mol, J.N. The flavonoid biosynthetic pathway in plants: Function and evolution. BioEssays 1994, 16, 123–132. [Google Scholar] [CrossRef]
  11. Shirley, B.W. Flavonoid biosynthesis:‘new’functions for an ‘old’pathway. Trends Plant Sci. 1996, 1, 377–382. [Google Scholar]
  12. Liu, W.; Feng, Y.; Yu, S.; Fan, Z.; Li, X.; Li, J.; Yin, H. The flavonoid biosynthesis network in plants. Int. J. Mol. Sci. 2021, 22, 12824. [Google Scholar] [CrossRef]
  13. Fraser, D.P.; Sharma, A.; Fletcher, T.; Budge, S.; Moncrieff, C.; Dodd, A.N.; Franklin, K.A. UV-B antagonises shade avoidance and increases levels of the flavonoid quercetin in coriander (Coriandrum sativum). Sci. Rep. 2017, 7, 17758. [Google Scholar] [CrossRef]
  14. Lois, R. Accumulation of UV-absorbing flavonoids induced by UV-B radiation in Arabidopsis thaliana L. Planta 1994, 194, 498–503. [Google Scholar] [CrossRef]
  15. Mattson, M.P. Hormesis defined. Ageing Res. Rev. 2008, 7, 1–7. [Google Scholar] [CrossRef]
  16. Lamming, D.W.; Wood, J.G.; Sinclair, D.A. Small molecules that regulate lifespan: Evidence for xenohormesis. Mol. Microbiol. 2004, 53, 1003–1009. [Google Scholar] [CrossRef] [PubMed]
  17. Cao, G.; Sofic, E.; Prior, R.L. Antioxidant and prooxidant behavior of flavonoids: Structure-activity relationships. Free Radic. Biol. Med. 1997, 22, 749–760. [Google Scholar] [CrossRef]
  18. Aherne, S.A.; O’Brien, N.M. Mechanism of protection by the flavonoids, quercetin and rutin, against tert-butylhydroperoxide- and menadione-induced DNA single strand breaks in Caco-2 cells. Free Radic. Biol. Med. 2000, 29, 507–514. [Google Scholar] [CrossRef]
  19. Zhang, M.; Lu, P.; Terada, T.; Sui, M.; Furuta, H.; Iida, K.; Katayama, Y.; Lu, Y.; Okamoto, K.; Suzuki, M. Quercetin 3, 5, 7, 3′, 4′-pentamethyl ether from Kaempferia parviflora directly and effectively activates human SIRT1. Commun. Biol. 2021, 4, 209. [Google Scholar] [CrossRef]
  20. Wei, X.; Jia, R.; Yang, Z.; Jiang, J.; Huang, J.; Yan, J.; Luo, X. NAD+/sirtuin metabolism is enhanced in response to cold-induced changes in lipid metabolism in mouse liver. FEBS Lett. 2020, 594, 1711–1725. [Google Scholar] [CrossRef] [PubMed]
  21. Chen, R.; Dioum, E.M.; Hogg, R.T.; Gerard, R.D.; Garcia, J.A. Hypoxia increases sirtuin 1 expression in a hypoxia-inducible factor-dependent manner. J. Biol. Chem. 2011, 286, 13869–13878. [Google Scholar] [PubMed]
  22. Crujeiras, A.; Parra, D.; Goyenechea, E.; Martínez, J. Sirtuin gene expression in human mononuclear cells is modulated by caloric restriction. Eur. J. Clin. Investig. 2008, 38, 672–678. [Google Scholar]
  23. Lazo-Gomez, R.; Tapia, R. Quercetin prevents spinal motor neuron degeneration induced by chronic excitotoxic stimulus by a sirtuin 1-dependent mechanism. Transl. Neurodegener. 2017, 6, 31. [Google Scholar] [CrossRef] [PubMed]
  24. Howitz, K.T.; Bitterman, K.J.; Cohen, H.Y.; Lamming, D.W.; Lavu, S.; Wood, J.G.; Zipkin, R.E.; Chung, P.; Kisielewski, A.; Zhang, L.-L.; et al. Small molecule activators of sirtuins extend Saccharomyces cerevisiae lifespan. Nature 2003, 425, 191–196. [Google Scholar] [CrossRef] [PubMed]
  25. van der Woude, H.; Ter Veld, M.G.; Jacobs, N.; van der Saag, P.T.; Murk, A.J.; Rietjens, I.M. The stimulation of cell proliferation by quercetin is mediated by the estrogen receptor. Mol. Nutr. Food Res. 2005, 49, 763–771. [Google Scholar] [CrossRef] [PubMed]
  26. Khanam, U.K.S.; Oba, S.; Yanase, E.; Murakami, Y. Phenolic acids, flavonoids and total antioxidant capacity of selected leafy vegetables. J. Funct. Foods 2012, 4, 979–987. [Google Scholar] [CrossRef]
  27. Sultana, B.; Anwar, F. Flavonols (kaempeferol, quercetin, myricetin) contents of selected fruits, vegetables and medicinal plants. Food Chem. 2008, 108, 879–884. [Google Scholar] [CrossRef]
  28. Barba, F.J.; Esteve, M.J.; Frígola, A. Bioactive components from leaf vegetable products. Stud. Nat. Prod. Chem. 2014, 41, 321–346. [Google Scholar]
  29. Poetschke, J.; Gauglitz, G.G. Onion extract. In Textbook on Scar Management: State of the Art Management and Emerging Technologies; Springer: Cham, Switzerland, 2020; pp. 209–213. [Google Scholar]
  30. Tziotzios, C.; Profyris, C.; Sterling, J. Cutaneous scarring: Pathophysiology, molecular mechanisms, and scar reduction therapeutics: Part II. Strategies to reduce scar formation after dermatologic procedures. J. Am. Acad. Dermatol. 2012, 66, 13–24. [Google Scholar] [CrossRef]
  31. Burak, C.; Brüll, V.; Langguth, P.; Zimmermann, B.F.; Stoffel-Wagner, B.; Sausen, U.; Stehle, P.; Wolffram, S.; Egert, S. Higher plasma quercetin levels following oral administration of an onion skin extract compared with pure quercetin dihydrate in humans. Eur. J. Nutr. 2017, 56, 343–353. [Google Scholar] [CrossRef]
  32. Mullen, W.; Edwards, C.A.; Crozier, A. Absorption, excretion and metabolite profiling of methyl-, glucuronyl-, glucosyl- and sulpho-conjugates of quercetin in human plasma and urine after ingestion of onions. Br. J. Nutr. 2006, 96, 107–116. [Google Scholar] [CrossRef]
  33. DuPont, M.S.; Bennett, R.N.; Mellon, F.A.; Williamson, G. Polyphenols from Alcoholic Apple Cider Are Absorbed, Metabolized and Excreted by Humans. J. Nutr. 2002, 132, 172–175. [Google Scholar] [CrossRef] [PubMed]
  34. Harwood, M.; Danielewska-Nikiel, B.; Borzelleca, J.; Flamm, G.; Williams, G.; Lines, T. A critical review of the data related to the safety of quercetin and lack of evidence of in vivo toxicity, including lack of genotoxic/carcinogenic properties. Food Chem. Toxicol. 2007, 45, 2179–2205. [Google Scholar] [CrossRef]
  35. Platzer, M.; Kiese, S.; Tybussek, T.; Herfellner, T.; Schneider, F.; Schweiggert-Weisz, U.; Eisner, P. Radical Scavenging Mechanisms of Phenolic Compounds: A Quantitative Structure-Property Relationship (QSPR) Study. Front. Nutr. 2022, 9, 882458. [Google Scholar] [CrossRef]
  36. McKay, T.B.; Kivanany, P.B.; Nicholas, S.E.; Nag, O.K.; Elliott, M.H.; Petroll, W.M.; Karamichos, D. Quercetin Decreases Corneal Haze In Vivo and Influences Gene Expression of TGF-Beta Mediators In Vitro. Metabolites 2022, 12, 626. [Google Scholar] [CrossRef]
  37. Du, L.; Hao, M.; Li, C.; Wu, W.; Wang, W.; Ma, Z.; Yang, T.; Zhang, N.; Isaac, A.T.; Zhu, X.; et al. Quercetin inhibited epithelial mesenchymal transition in diabetic rats, high-glucose-cultured lens, and SRA01/04 cells through transforming growth factor-β2/phosphoinositide 3-kinase/Akt pathway. Mol. Cell Endocrinol. 2017, 452, 44–56. [Google Scholar] [CrossRef]
  38. Lu, Q.; Hao, M.; Wu, W.; Zhang, N.; Isaac, A.T.; Yin, J.; Zhu, X.; Du, L.; Yin, X. Antidiabetic cataract effects of GbE, rutin and quercetin are mediated by the inhibition of oxidative stress and polyol pathway. Acta Biochim. Pol. 2018, 65, 35–41. [Google Scholar] [CrossRef]
  39. Oh, H.N.; Kim, C.E.; Lee, J.H.; Yang, J.W. Effects of quercetin in a mouse model of experimental dry eye. Cornea 2015, 34, 1130–1136. [Google Scholar] [CrossRef]
  40. Abengózar-Vela, A.; Schaumburg, C.S.; Stern, M.E.; Calonge, M.; Enríquez-de-Salamanca, A.; González-García, M.J. Topical quercetin and resveratrol protect the ocular surface in experimental dry eye disease. Ocul. Immunol. Inflamm. 2019, 27, 1023–1032. [Google Scholar] [CrossRef]
  41. Horton, J.A.; Li, F.; Chung, E.J.; Hudak, K.; White, A.; Krausz, K.; Gonzalez, F.; Citrin, D. Quercetin inhibits radiation-induced skin fibrosis. Radiat. Res. 2013, 180, 205–215. [Google Scholar] [CrossRef] [PubMed]
  42. Yang, N.; Shi, N.; Yao, Z.; Liu, H.; Guo, W. Gallium-modified gelatin nanoparticles loaded with quercetin promote skin wound healing via the regulation of bacterial proliferation and macrophage polarization. Front. Bioeng. Biotechnol. 2023, 11, 1124944. [Google Scholar] [CrossRef] [PubMed]
  43. Chen, Y.J.; Cheng, H.W.; Yen, W.Y.; Tsai, J.H.; Yeh, C.Y.; Chen, C.J.; Liu, J.T.; Chen, S.Y.; Chang, S.J. The Treatment of Keloid Scars via Modulating Heterogeneous Gelatin-Structured Composite Microneedles to Control Transdermal Dual-Drug Release. Polymers 2022, 14, 4436. [Google Scholar] [CrossRef] [PubMed]
  44. Fu, J.; Huang, J.; Lin, M.; Xie, T.; You, T. Quercetin Promotes Diabetic Wound Healing via Switching Macrophages From M1 to M2 Polarization. J. Surg. Res. 2020, 246, 213–223. [Google Scholar] [CrossRef]
  45. Jee, J.-P.; Pangeni, R.; Jha, S.K.; Byun, Y.; Park, J.W. Preparation and in vivo evaluation of a topical hydrogel system incorporating highly skin-permeable growth factors, quercetin, and oxygen carriers for enhanced diabetic wound-healing therapy. Int. J. Nanomed. 2019, 14, 5449–5475. [Google Scholar] [CrossRef]
  46. Shisheva, A.; Shechter, Y. Quercetin selectively inhibits insulin receptor function in vitro and the bioresponses of insulin and insulinomimetic agents in rat adipocytes. Biochemistry 1992, 31, 8059–8063. [Google Scholar] [CrossRef]
  47. Jung, C.H.; Cho, I.; Ahn, J.; Jeon, T.I.; Ha, T.Y. Quercetin reduces high-fat diet-induced fat accumulation in the liver by regulating lipid metabolism genes. Phytother. Res. 2013, 27, 139–143. [Google Scholar] [CrossRef]
  48. Yang, D.K.; Kang, H.S. Anti-Diabetic Effect of Cotreatment with Quercetin and Resveratrol in Streptozotocin-Induced Diabetic Rats. Biomol. Ther. 2018, 26, 130–138. [Google Scholar] [CrossRef]
  49. Kottmann, R.M.; Kulkarni, A.A.; Smolnycki, K.A.; Lyda, E.; Dahanayake, T.; Salibi, R.; Honnons, S.; Jones, C.; Isern, N.G.; Hu, J.Z. Lactic acid is elevated in idiopathic pulmonary fibrosis and induces myofibroblast differentiation via pH-dependent activation of transforming growth factor-β. Am. J. Respir. Crit. Care Med. 2012, 186, 740–751. [Google Scholar] [CrossRef] [PubMed]
  50. Cui, H.; Xie, N.; Banerjee, S.; Ge, J.; Jiang, D.; Dey, T.; Matthews, Q.L.; Liu, R.-M.; Liu, G. Lung myofibroblasts promote macrophage profibrotic activity through lactate-induced histone lactylation. Am. J. Respir. Cell Mol. Biol. 2021, 64, 115–125. [Google Scholar] [CrossRef]
  51. Nakamura, T.; Matsushima, M.; Hayashi, Y.; Shibasaki, M.; Imaizumi, K.; Hashimoto, N.; Shimokata, K.; Hasegawa, Y.; Kawabe, T. Attenuation of transforming growth factor-β-stimulated collagen production in fibroblasts by quercetin-induced heme oxygenase-1. Am. J. Respir. Cell Mol. Biol. 2011, 44, 614–620. [Google Scholar] [CrossRef] [PubMed]
  52. Veith, C.; Drent, M.; Bast, A.; van Schooten, F.J.; Boots, A.W. The disturbed redox-balance in pulmonary fibrosis is modulated by the plant flavonoid quercetin. Toxicol. Appl. Pharmacol. 2017, 336, 40–48. [Google Scholar] [CrossRef] [PubMed]
  53. McKay, T.B.; Lyon, D.; Sarker-Nag, A.; Priyadarsini, S.; Asara, J.M.; Karamichos, D. Quercetin attenuates lactate production and extracellular matrix secretion in keratoconus. Sci. Rep. 2015, 5, 9003. [Google Scholar] [CrossRef] [PubMed]
  54. Karamichos, D.; Hutcheon, A.E.; Rich, C.B.; Trinkaus-Randall, V.; Asara, J.M.; Zieske, J.D. In vitro model suggests oxidative stress involved in keratoconus disease. Sci. Rep. 2014, 4, 4608. [Google Scholar] [CrossRef]
  55. McKay, T.B.; Sarker-Nag, A.; Lyon, D.; Asara, J.M.; Karamichos, D. Quercetin modulates keratoconus metabolism in vitro. Cell Biochem. Funct. 2015, 33, 341–350. [Google Scholar] [CrossRef] [PubMed]
  56. Jia, L.; Huang, S.; Yin, X.; Zan, Y.; Guo, Y.; Han, L. Quercetin suppresses the mobility of breast cancer by suppressing glycolysis through Akt-mTOR pathway mediated autophagy induction. Life Sci. 2018, 208, 123–130. [Google Scholar] [CrossRef]
  57. Pani, S.; Sahoo, A.; Patra, A.; Debata, P.R. Phytocompounds curcumin, quercetin, indole-3-carbinol, and resveratrol modulate lactate-pyruvate level along with cytotoxic activity in HeLa cervical cancer cells. Biotechnol. Appl. Biochem. 2021, 68, 1396–1402. [Google Scholar] [CrossRef]
  58. Vander Heiden, M.G.; Cantley, L.C.; Thompson, C.B. Understanding the Warburg effect: The metabolic requirements of cell proliferation. Science 2009, 324, 1029–1033. [Google Scholar] [CrossRef] [PubMed]
  59. Mi, Y.; Zhong, L.; Lu, S.; Hu, P.; Pan, Y.; Ma, X.; Yan, B.; Wei, Z.; Yang, G. Quercetin promotes cutaneous wound healing in mice through Wnt/β-catenin signaling pathway. J. Ethnopharmacol. 2022, 290, 115066. [Google Scholar] [CrossRef]
  60. Jalali, M.; Bayat, A. Current use of steroids in management of abnormal raised skin scars. Surgeon 2007, 5, 175–180. [Google Scholar] [CrossRef] [PubMed]
  61. Beken, B.; Serttas, R.; Yazicioglu, M.; Turkekul, K.; Erdogan, S. Quercetin Improves Inflammation, Oxidative Stress, and Impaired Wound Healing in Atopic Dermatitis Model of Human Keratinocytes. Pediatr. Allergy Immunol. Pulmonol. 2020, 33, 69–79. [Google Scholar] [CrossRef] [PubMed]
  62. Li, F.; Bai, Y.; Zhao, M.; Huang, L.; Li, S.; Li, X.; Chen, Y. Quercetin inhibits vascular endothelial growth factor-induced choroidal and retinal angiogenesis in vitro. Ophthalmic Res. 2015, 53, 109–116. [Google Scholar] [CrossRef]
  63. Lupo, G.; Cambria, M.T.; Olivieri, M.; Rocco, C.; Caporarello, N.; Longo, A.; Zanghì, G.; Salmeri, M.; Foti, M.C.; Anfuso, C.D. Anti-angiogenic effect of quercetin and its 8-methyl pentamethyl ether derivative in human microvascular endothelial cells. J. Cell. Mol. Med. 2019, 23, 6565–6577. [Google Scholar] [CrossRef]
  64. López-Otín, C.; Blasco, M.A.; Partridge, L.; Serrano, M.; Kroemer, G. Hallmarks of aging: An expanding universe. Cell 2023, 186, 243–278. [Google Scholar] [CrossRef]
  65. Wood, J.G.; Rogina, B.; Lavu, S.; Howitz, K.; Helfand, S.L.; Tatar, M.; Sinclair, D. Sirtuin activators mimic caloric restriction and delay ageing in metazoans. Nature 2004, 430, 686–689. [Google Scholar] [CrossRef]
  66. Baur, J.A.; Pearson, K.J.; Price, N.L.; Jamieson, H.A.; Lerin, C.; Kalra, A.; Prabhu, V.V.; Allard, J.S.; Lopez-Lluch, G.; Lewis, K.; et al. Resveratrol improves health and survival of mice on a high-calorie diet. Nature 2006, 444, 337–342. [Google Scholar] [CrossRef]
  67. Sun, Y.; Yang, Y.M.; Hu, Y.Y.; Ouyang, L.; Sun, Z.H.; Yin, X.F.; Li, N.; He, Q.Y.; Wang, Y. Inhibition of nuclear deacetylase Sirtuin-1 induces mitochondrial acetylation and calcium overload leading to cell death. Redox Biol. 2022, 53, 102334. [Google Scholar] [CrossRef]
  68. Gurd, B.J. Deacetylation of PGC-1α by SIRT1: Importance for skeletal muscle function and exercise-induced mitochondrial biogenesis. Appl. Physiol. Nutr. Metab. 2011, 36, 589–597. [Google Scholar] [CrossRef] [PubMed]
  69. Belinha, I.; Amorim, M.A.; Rodrigues, P.; de Freitas, V.; Moradas-Ferreira, P.; Mateus, N.; Costa, V. Quercetin increases oxidative stress resistance and longevity in Saccharomyces cerevisiae. J. Agric. Food Chem. 2007, 55, 2446–2451. [Google Scholar] [CrossRef] [PubMed]
  70. Scambia, G.; Mancuso, S.; Panici, P.B.; De Vincenzo, R.; Ferrandina, G.; Bonanno, G.; Ranelletti, F.O.; Piantelli, M.; Capelli, A. Quercetin induces type-II estrogen-binding sites in estrogen-receptor-negative (MDA-MB231) and estrogen-receptor-positive (MCF-7) human breast-cancer cell lines. Int. J. Cancer 1993, 54, 462–466. [Google Scholar] [CrossRef]
  71. Redza-Dutordoir, M.; Averill-Bates, D.A. Activation of apoptosis signalling pathways by reactive oxygen species. Biochim. Biophys. Acta 2016, 1863, 2977–2992. [Google Scholar] [CrossRef] [PubMed]
  72. Iside, C.; Scafuro, M.; Nebbioso, A.; Altucci, L. SIRT1 Activation by Natural Phytochemicals: An Overview. Front. Pharmacol. 2020, 11, 1225. [Google Scholar] [CrossRef] [PubMed]
  73. Moutsatsou, P. The spectrum of phytoestrogens in nature: Our knowledge is expanding. HORMONES-ATHENS- 2007, 6, 173. [Google Scholar]
  74. Björnström, L.; Sjöberg, M. Mechanisms of Estrogen Receptor Signaling: Convergence of Genomic and Nongenomic Actions on Target Genes. Mol. Endocrinol. 2005, 19, 833–842. [Google Scholar] [CrossRef] [PubMed]
  75. Zhao, J.; Yang, J.; Xie, Y. Improvement strategies for the oral bioavailability of poorly water-soluble flavonoids: An overview. Int. J. Pharm. 2019, 570, 118642. [Google Scholar] [CrossRef] [PubMed]
  76. Wu, J.; Chen, Y.; Liu, X.; Gao, Y.; Hu, J.; Chen, H. Discovery of novel negletein derivatives as potent anticancer agents for acute myeloid leukemia. Chem. Biol. Drug Des. 2018, 91, 924–932. [Google Scholar] [CrossRef]
  77. Yang, A.; Liu, C.; Zhang, H.; Wu, J.; Shen, R.; Kou, X. A multifunctional anti-AD approach: Design, synthesis, X-ray crystal structure, biological evaluation and molecular docking of chrysin derivatives. Eur. J. Med. Chem. 2022, 233, 114216. [Google Scholar] [CrossRef] [PubMed]
  78. Lee, Y.H.; Kim, H.J.; Yoo, H.; Jung, S.Y.; Kwon, B.J.; Kim, N.J.; Jin, C.; Lee, Y.S. Synthesis of (2-amino)ethyl derivatives of quercetin 3-O-methyl ether and their antioxidant and neuroprotective effects. Bioorg Med. Chem. 2015, 23, 4970–4979. [Google Scholar] [CrossRef] [PubMed]
  79. Sun, J.; Li, F.; Zhao, Y.; Zhao, L.; Qiao, C.; Li, Z.; Guo, Q.; Lu, N. LZ-207, a Newly Synthesized Flavonoid, Induces Apoptosis and Suppresses Inflammation-Related Colon Cancer by Inhibiting the NF-kappaB Signaling Pathway. PLoS ONE 2015, 10, e0127282. [Google Scholar] [CrossRef]
  80. Helgren, T.R.; Sciotti, R.J.; Lee, P.; Duffy, S.; Avery, V.M.; Igbinoba, O.; Akoto, M.; Hagen, T.J. The synthesis, antimalarial activity and CoMFA analysis of novel aminoalkylated quercetin analogs. Bioorg. Med. Chem. Lett. 2015, 25, 327–332. [Google Scholar] [CrossRef] [PubMed]
  81. Mukherjee, A.; Mishra, S.; Kotla, N.K.; Manna, K.; Roy, S.; Kundu, B.; Bhattacharya, D.; Das Saha, K.; Talukdar, A. Semisynthetic Quercetin Derivatives with Potent Antitumor Activity in Colon Carcinoma. ACS Omega 2019, 4, 7285–7298. [Google Scholar] [CrossRef]
  82. Chen, H.; Mrazek, A.A.; Wang, X.; Ding, C.; Ding, Y.; Porro, L.J.; Liu, H.; Chao, C.; Hellmich, M.R.; Zhou, J. Design, synthesis, and characterization of novel apigenin analogues that suppress pancreatic stellate cell proliferation in vitro and associated pancreatic fibrosis in vivo. Bioorg. Med. Chem. 2014, 22, 3393–3404. [Google Scholar] [CrossRef] [PubMed]
  83. Wang, J.; Li, T.; Zhao, T.; Wu, T.; Liu, C.; Ding, H.; Li, Z.; Bian, J. Design of wogonin-inspired selective cyclin-dependent kinase 9 (CDK9) inhibitors with potent in vitro and in vivo antitumor activity. Eur. J. Med. Chem. 2019, 178, 782–801. [Google Scholar] [CrossRef]
  84. Feng, S.; Zhou, H.; Wu, D.; Zheng, D.; Qu, B.; Liu, R.; Zhang, C.; Li, Z.; Xie, Y.; Luo, H.B. Nobiletin and its derivatives overcome multidrug resistance (MDR) in cancer: Total synthesis and discovery of potent MDR reversal agents. Acta Pharm. Sin. B 2020, 10, 327–343. [Google Scholar] [CrossRef] [PubMed]
  85. Lombardo, E.; Sabellico, C.; Hajek, J.; Stankova, V.; Filipsky, T.; Balducci, V.; De Vito, P.; Leone, S.; Bavavea, E.I.; Silvestri, I.P.; et al. Protection of cells against oxidative stress by nanomolar levels of hydroxyflavones indicates a new type of intracellular antioxidant mechanism. PLoS ONE 2013, 8, e60796. [Google Scholar] [CrossRef] [PubMed]
  86. Zhu, S.; Yang, C.; Zhang, L.; Wang, S.; Ma, M.; Zhao, J.; Song, Z.; Wang, F.; Qu, X.; Li, F.; et al. Development of M10, myricetin-3-O-beta-d-lactose sodium salt, a derivative of myricetin as a potent agent of anti-chronic colonic inflammation. Eur. J. Med. Chem. 2019, 174, 9–15. [Google Scholar] [CrossRef] [PubMed]
  87. Li, F.; Yang, C.; Zhang, L.; Li, W. Synthesis of myricetin derivatives and evaluation of their hypoglycemic activities. Med. Chem. Res. 2023, 32, 76–84. [Google Scholar] [CrossRef]
  88. Li, M.; Li, Y.; Ludwik, K.A.; Sandusky, Z.M.; Lannigan, D.A.; O’Doherty, G.A. Stereoselective Synthesis and Evaluation of C6’’-Substituted 5a-Carbasugar Analogues of SL0101 as Inhibitors of RSK1/2. Org. Lett. 2017, 19, 2410–2413. [Google Scholar] [CrossRef]
  89. Seley-Radtke, K.L.; Yates, M.K. The evolution of nucleoside analogue antivirals: A review for chemists and non-chemists. Part 1: Early structural modifications to the nucleoside scaffold. Antivir. Res. 2018, 154, 66–86. [Google Scholar] [CrossRef]
  90. Ludwik, K.A.; Campbell, J.P.; Li, M.; Li, Y.; Sandusky, Z.M.; Pasic, L.; Sowder, M.E.; Brenin, D.R.; Pietenpol, J.A.; O’Doherty, G.A.; et al. Development of a RSK Inhibitor as a Novel Therapy for Triple-Negative Breast Cancer. Mol Cancer Ther. 2016, 15, 2598–2608. [Google Scholar] [CrossRef]
  91. Xu, D.; Hu, M.J.; Wang, Y.Q.; Cui, Y.L. Antioxidant Activities of Quercetin and Its Complexes for Medicinal Application. Molecules 2019, 24, 1123. [Google Scholar] [CrossRef] [PubMed]
  92. Suganthy, N.; Devi, K.P.; Nabavi, S.F.; Braidy, N.; Nabavi, S.M. Bioactive effects of quercetin in the central nervous system: Focusing on the mechanisms of actions. Biomed. Pharmacother. 2016, 84, 892–908. [Google Scholar] [CrossRef] [PubMed]
  93. Qi, Y.; Guo, L.; Jiang, Y.; Shi, Y.; Sui, H.; Zhao, L. Brain delivery of quercetin-loaded exosomes improved cognitive function in AD mice by inhibiting phosphorylated tau-mediated neurofibrillary tangles. Drug Deliv. 2020, 27, 745–755. [Google Scholar] [CrossRef]
  94. Wang, S.; Chen, Y.; Xia, C.; Yang, C.; Chen, J.; Hai, L.; Wu, Y.; Yang, Z. Synthesis and evaluation of glycosylated quercetin to enhance neuroprotective effects on cerebral ischemia-reperfusion. Bioorg. Med. Chem. 2022, 73, 117008. [Google Scholar] [CrossRef] [PubMed]
  95. Tron, G.C.; Pirali, T.; Billington, R.A.; Canonico, P.L.; Sorba, G.; Genazzani, A.A. Click chemistry reactions in medicinal chemistry: Applications of the 1,3-dipolar cycloaddition between azides and alkynes. Med. Res. Rev. 2008, 28, 278–308. [Google Scholar] [CrossRef] [PubMed]
  96. Matos, A.M.; Man, T.; Idrissi, I.; Souza, C.C.; Mead, E.; Dunbar, C.; Wolak, J.; Oliveira, M.C.; Evans, D.; Grayson, J.; et al. Discovery of N-methylpiperazinyl flavones as a novel class of compounds with therapeutic potential against Alzheimer’s disease: Synthesis, binding affinity towards amyloid β oligomers (Aβo) and ability to disrupt Aβo-PrPC interactions. Pure Appl. Chem. 2019, 91, 1107–1136. [Google Scholar] [CrossRef]
  97. Kandemir, K.; Tomas, M.; McClements, D.J.; Capanoglu, E. Recent advances on the improvement of quercetin bioavailability. Trends Food Sci. Technol. 2022, 119, 192–200. [Google Scholar] [CrossRef]
Bioengineering 10 01127 g002
Figure 2. Quercetin and structurally related flavonoid natural products.
Figure 2. Quercetin and structurally related flavonoid natural products.
Bioengineering 10 01127 g002
Bioengineering 10 01127 g003
Figure 3. Synthetic flavonoids employing basic amine-containing groups as a means to improve physiochemical and/or pharmacological properties. Synthetic modifications to the parent natural product are highlighted with dashed-lines.
Figure 3. Synthetic flavonoids employing basic amine-containing groups as a means to improve physiochemical and/or pharmacological properties. Synthetic modifications to the parent natural product are highlighted with dashed-lines.
Bioengineering 10 01127 g003
Bioengineering 10 01127 g004
Figure 4. Synthetic flavonoids employing sugars as a means to improve physiochemical and/or pharmacological properties. Synthetic modifications to the parent natural product are highlighted with dashed-lines.
Figure 4. Synthetic flavonoids employing sugars as a means to improve physiochemical and/or pharmacological properties. Synthetic modifications to the parent natural product are highlighted with dashed-lines.
Bioengineering 10 01127 g004
Table 1. Selected preclinical evidence in animal models for the biological effects of quercetin in promoting tissue repair and anti-scarring properties in the anterior segment of the eye.
Table 1. Selected preclinical evidence in animal models for the biological effects of quercetin in promoting tissue repair and anti-scarring properties in the anterior segment of the eye.
Biological
Properties		Model
System		InjuryDrug
Treatment		ResultsRef.
AntifibroticC57BL/6J miceCorneal epithelial and stromal debridementTopical ocular application of 5 mM quercetinReduction in corneal opacity based on slit lamp[36]
New Zealand white rabbitsCorneal lamellar keratectomyTopical ocular application of 5 mM quercetinReduction in corneal haze based on in vivo confocal microscopy[36]
AntioxidativeSprague- Dawley ratsSTZ treatment to induce diabetes-associated complications30–120 mg/kg quercetin administered i.g.Reduced lens opacity based on slit lamp and decreased AGEs[37]
Sprague-Dawley ratsSTZ treatment to induce hyperglycemia90 mg/kg quercetin i.p.Reduced lens opacity based on slit lamp and increased GSH production[38]
Anti-inflammatoryNOD.B10.H2 miceInjection of muscarinic receptor blocker followed by desiccation for 10 days to induce dry eye symptomsTopical ocular application of 0.5% w/v quercetinIncreased tear production and reduced pro-inflammatory cytokine secretion[39]
WT C57BL/6 and T-cell-deficient C57BL/6 miceDesiccation for 10 days and continuous injection of scopolamine hydrobromide to induce dry eye symptomsTopical ocular application of 0.01% w/v quercetinImproved ocular surface barrier function and decreased pro-inflammatory cytokine secretion[40]
(Abbreviations: advanced glycation end products (AGEs); intragastric infusion (i.g.); intraperitoneal (i.p.); milligrams of quercetin per animal weight in kilograms (mg/kg); millimolar (mM); streptozotocin (STZ); weight to volume (w/v); wild-type (WT)).
Disclaimer/Publisher’s Note: The statements, opinions and data contained in all publications are solely those of the individual author(s) and contributor(s) and not of MDPI and/or the editor(s). MDPI and/or the editor(s) disclaim responsibility for any injury to people or property resulting from any ideas, methods, instructions or products referred to in the content.

Share and Cite

MDPI and ACS Style

McKay, T.B.; Emmitte, K.A.; German, C.; Karamichos, D. Quercetin and Related Analogs as Therapeutics to Promote Tissue Repair. Bioengineering 2023, 10, 1127. https://doi.org/10.3390/bioengineering10101127

AMA Style

McKay TB, Emmitte KA, German C, Karamichos D. Quercetin and Related Analogs as Therapeutics to Promote Tissue Repair. Bioengineering. 2023; 10(10):1127. https://doi.org/10.3390/bioengineering10101127

Chicago/Turabian Style

McKay, Tina B., Kyle A. Emmitte, Carrie German, and Dimitrios Karamichos. 2023. "Quercetin and Related Analogs as Therapeutics to Promote Tissue Repair" Bioengineering 10, no. 10: 1127. https://doi.org/10.3390/bioengineering10101127

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop