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Mangiferin induces islet regeneration in aged mice through regulating p16(INK4a)
Previous studies by our group on mangiferin demonstrated that it exerts an antihyperglycemic 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,...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
D.A. Spandidos
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5881804/ https://www.ncbi.nlm.nih.gov/pubmed/29512742 http://dx.doi.org/10.3892/ijmm.2018.3524 |
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author | Wang, Hailian He, Xia Lei, Tiantian Liu, Yilong Huai, Guoli Sun, Minghan Deng, Shaoping Yang, Hongji Tong, Rongsheng Wang, Yi |
author_facet | Wang, Hailian He, Xia Lei, Tiantian Liu, Yilong Huai, Guoli Sun, Minghan Deng, Shaoping Yang, Hongji Tong, Rongsheng Wang, Yi |
author_sort | Wang, Hailian |
collection | PubMed |
description | Previous studies by our group on mangiferin demonstrated that it exerts an antihyperglycemic 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 p27(Kip1) and p16(INK4a) 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 p16(INK4a), suggesting that mangiferin induced β-cell proliferation via the regulation of p16(INK4a). 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. |
format | Online Article Text |
id | pubmed-5881804 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | D.A. Spandidos |
record_format | MEDLINE/PubMed |
spelling | pubmed-58818042018-04-12 Mangiferin induces islet regeneration in aged mice through regulating p16(INK4a) Wang, Hailian He, Xia Lei, Tiantian Liu, Yilong Huai, Guoli Sun, Minghan Deng, Shaoping Yang, Hongji Tong, Rongsheng Wang, Yi Int J Mol Med Articles Previous studies by our group on mangiferin demonstrated that it exerts an antihyperglycemic 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 p27(Kip1) and p16(INK4a) 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 p16(INK4a), suggesting that mangiferin induced β-cell proliferation via the regulation of p16(INK4a). 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. D.A. Spandidos 2018-06 2018-03-01 /pmc/articles/PMC5881804/ /pubmed/29512742 http://dx.doi.org/10.3892/ijmm.2018.3524 Text en Copyright: © Wang et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made. |
spellingShingle | Articles Wang, Hailian He, Xia Lei, Tiantian Liu, Yilong Huai, Guoli Sun, Minghan Deng, Shaoping Yang, Hongji Tong, Rongsheng Wang, Yi Mangiferin induces islet regeneration in aged mice through regulating p16(INK4a) |
title | Mangiferin induces islet regeneration in aged mice through regulating p16(INK4a) |
title_full | Mangiferin induces islet regeneration in aged mice through regulating p16(INK4a) |
title_fullStr | Mangiferin induces islet regeneration in aged mice through regulating p16(INK4a) |
title_full_unstemmed | Mangiferin induces islet regeneration in aged mice through regulating p16(INK4a) |
title_short | Mangiferin induces islet regeneration in aged mice through regulating p16(INK4a) |
title_sort | mangiferin induces islet regeneration in aged mice through regulating p16(ink4a) |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5881804/ https://www.ncbi.nlm.nih.gov/pubmed/29512742 http://dx.doi.org/10.3892/ijmm.2018.3524 |
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