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Mangiferin induces islet regeneration in aged mice through regulating p16INK4a
Hailian Wang1, Xia He2, Tiantian Lei3
1Institute of Organ Transplantation, Sichuan Academy of Medical Science and Sichuan Provincial People's Hospital, Chengdu, Sichuan 610072, P.R. China.
Abstract:
Previous studies by our group on mangiferin demonstrated that it exerts an anti‑hyperglycemic effect through the regulation of cell cycle proteins in 3‑month‑old, partially pancreatectomized (PPx) mice. However, β‑cell proliferation is known to become severely restricted with advanced age. Therefore, it is unknown whether mangiferin is able to reverse the diabetic condition and retain β‑cell regeneration capability in aged mice. In the present study, 12‑month‑old C57BL/6J mice that had undergone PPx were subjected to mangiferin treatment (90 mg/kg) for 28 days. Mangiferin‑treated aged mice exhibited decreased blood glucose levels and increased glucose tolerance, which was accompanied with higher serum insulin levels when compared with those in untreated PPx control mice. In addition, islet hyperplasia, elevated β‑cell proliferation and reduced β‑cell apoptosis were also identified in the mice that received mangiferin treatment. Further studies on the mRNA transcript and protein expression levels indicated comparatively increased levels of cyclins D1 and D2 and cyclin‑dependent kinase 4 in mangiferin‑treated mice, while the levels of p27Kip1 and p16INK4a were decreased relative to those in the untreated PPx controls. Of note, mangiferin treatment improved the proliferation rate of islet β‑cells in adult mice overexpressing p16INK4a, suggesting that mangiferin induced β‑cell proliferation via the regulation of p16INK4a. In addition, the mRNA transcription levels of critical genes associated with insulin secretion, including pancreatic and duodenal homeobox 1, glucose transporter 2 and glucokinase, were observed to be upregulated after mangiferin treatment. Taken together, it was indicated that mangiferin treatment significantly induced β‑cell proliferation and inhibited β‑cell apoptosis by regulating cell cycle checkpoint proteins. Furthermore, mangiferin was also demonstrated to regulate genes associated with insulin secretion. Collectively these, results suggest the therapeutic potential of mangiferin in the treatment of diabetes in aged individuals.
Insights
Mangiferin treatment improved blood glucose control and insulin levels in aged diabetic mice. It promoted beta-cell regeneration by regulating cell cycle proteins and enhancing insulin secretion genes.
Area of Science:
- Endocrinology
- Gerontology
- Pharmacology
Background:
- Mangiferin shows anti-hyperglycemic effects by regulating cell cycle proteins in younger mice.
- Beta-cell proliferation capacity diminishes significantly with advanced age.
- The efficacy of mangiferin in aged diabetic models remains unexplored.
Purpose of the Study:
- To investigate mangiferin's potential to reverse diabetes and promote beta-cell regeneration in aged mice.
- To elucidate the molecular mechanisms underlying mangiferin's effects on beta-cells in aging individuals.
Main Methods:
- Aged partially pancreatectomized (PPx) mice were treated with mangiferin (90 mg/kg) for 28 days.
- Assessed blood glucose, glucose tolerance, serum insulin, islet morphology, beta-cell proliferation, and apoptosis.
- Analyzed mRNA and protein expression of cell cycle regulators (cyclins D1/D2, CDK4, p27Kip1, p16INK4a) and insulin secretion genes (PDX1, GLUT2, GK).
Main Results:
- Mangiferin treatment decreased blood glucose and improved glucose tolerance, with increased serum insulin levels.
- Observed islet hyperplasia, enhanced beta-cell proliferation, and reduced beta-cell apoptosis in mangiferin-treated mice.
- Mangiferin upregulated cyclins D1/D2, CDK4, and insulin secretion genes (PDX1, GLUT2, GK), while downregulating p27Kip1 and p16INK4a, suggesting a role in beta-cell proliferation via p16INK4a regulation.
Conclusions:
- Mangiferin effectively induces beta-cell proliferation and inhibits apoptosis in aged diabetic mice by modulating cell cycle checkpoint proteins.
- Mangiferin also regulates key genes involved in insulin secretion, indicating a comprehensive therapeutic effect.
- These findings highlight mangiferin's therapeutic potential for treating diabetes in aged populations.
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