Animal Models of Pancreatic Diseases

A special issue of Biology (ISSN 2079-7737). This special issue belongs to the section "Physiology".

Deadline for manuscript submissions: 31 December 2024 | Viewed by 632

Special Issue Editors


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Guest Editor
Department of Surgery, University of Virginia School of Medicine, Charlottesville, VA 22908, USA
Interests: pancreas; type 1 diabetes; islet transplantation; immunology; immunotherapies; biochemistry

E-Mail Website
Guest Editor
Department of Surgery, University of Virginia School of Medicine, Charlottesville, VA 22908, USA
Interests: kidney, pancreas and islet transplant; transplantation tolerance; gene therapy; xenotransplantation; transplant immunosuppression; pancreas

Special Issue Information

Dear Colleagues,

Animal models play a pivotal role in advancing our understanding of pancreatic diseases, including pancreatitis, pancreatic cancer and diabetes. These models, predominantly rodents, provide valuable insights into the etiology, pathogenesis and potential therapeutic interventions for these conditions. For example, in the context of pancreatitis, both acute and chronic forms have been replicated in rodents through methods such as cerulein administration or ethanol exposure. These studies have been instrumental in elucidating the inflammatory cascades and fibrotic changes observed in human pancreatitis and have helped identify potential therapeutic targets. In the realm of pancreatic cancer research, genetically engineered mouse models (GEMMs) simulate human pancreatic cancer development by introducing key mutations such as Kras, p53 and Smad4 mutations. This enables researchers to investigate various stages of tumor development, from initiation to metastasis. Additionally, xenograft and patient-derived xenograft (PDX) models, that involve the transplantation of human tumor cells or tissues into mice, provide invaluable platforms for testing novel anticancer therapies and personalized medicine approaches. In diabetes research, several animal models have been employed to study both type 1 and type 2 diabetes. For instance, the non-obese diabetic (NOD) mouse model has played a pivotal role in elucidating the autoimmune basis of type 1 diabetes. Chemically induced models, such as streptozotocin-treated rodents, closely mimic the beta-cell destruction characteristic of autoimmune diabetes, and have helped delineate underlying mechanisms, discover novel immunotherapies for promoting islet or pancreas graft survival, and identify potential regenerative therapies. Diet-induced obesity rodents and genetically modified mice (e.g., ob/ob and db/db) have been instrumental in replicating insulin resistance and obesity, key features of type 2 diabetes, and facilitating research on insulin signaling pathways and glucose metabolism. Animal models also serve as vital platforms for the preclinical testing of potential treatments, guiding therapeutic development and contributing to improved patient outcomes in pancreatic diseases. This Special Issue explores novel and diverse animal models used in pancreatic disease research, and highlights the key findings and contributions made to date. 

Dr. Preeti Chhabra
Dr. Kenneth Brayman
Guest Editors

Manuscript Submission Information

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Keywords

  • animal models
  • pancreatic diseases
  • pancreatitis
  • pancreatic cancer
  • diabetes
  • pathogenesis
  • therapeutic targets
  • preclinical testing

Published Papers (1 paper)

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Research

14 pages, 5747 KiB  
Article
Mesenchymal Stem Cell-Derived Exosomes Loaded with Selenium or Nano Selenium as a Novel Therapeutic Paradigm for Streptozotocin-Induced Type 1 Diabetes in Rats
by Dlovan Y. Khalil, Ridah H. Hussein and Wafaa M. El-Kholy
Biology 2024, 13(4), 253; https://doi.org/10.3390/biology13040253 - 11 Apr 2024
Viewed by 503
Abstract
Type 1 diabetes mellitus (T1DM) is a metabolic disorder characterized by hyperglycemia due to insulin insufficiency as a consequence of the pancreatic β-cells’ auto-immune attack. Nowadays, the application of mesenchymal stem cell-derived exosomes (MSCs-Exs) as the main cell-free therapy for diabetes treatment is [...] Read more.
Type 1 diabetes mellitus (T1DM) is a metabolic disorder characterized by hyperglycemia due to insulin insufficiency as a consequence of the pancreatic β-cells’ auto-immune attack. Nowadays, the application of mesenchymal stem cell-derived exosomes (MSCs-Exs) as the main cell-free therapy for diabetes treatment is becoming more and more extensive. In non-autologous therapy, researchers are moving towards a new strategy based on loading MSC-Exs with certain drugs, aimed at maintaining and maximizing the function of exosomes at the function site and enhancing their efficiency and safety. This study aims to explore and compare the therapeutic potentialities of mesenchymal stem cell-derived exosomes (MSCs-Exs) loaded with either selenium (Se) or nano selenium (NSe), a natural antioxidant micronutrient, in the management of T1DM in rats. In our 4-week experiment, six rat groups were included, namely, control, Ex+Se, Ex+NSe, STZ-diabetic (D), D+ Ex+Se, and D+Ex+NSe groups. Both diabetic-treated groups showed marked pancreatic regenerative antioxidant, immunomodulatory, anti-inflammatory, and anti-apoptotic capacities, with the D+Ex+NSe injection showing superiority in managing diabetes hazards, as evidenced by various biochemical and histological assessments. Full article
(This article belongs to the Special Issue Animal Models of Pancreatic Diseases)
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