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Effects of Simvastatin on Glucose Metabolism in Mouse MIN6 Cells

The aim of this study was to investigate the effects of simvastatin on insulin secretion in mouse MIN6 cells and the possible mechanism. MIN6 cells were, respectively, treated with 0 μM, 2 μM, 5 μM, and 10 μM simvastatin for 48 h. Radio immunoassay was performed to measure the effect of simvastatin...

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Autores principales: Zhou, Jieqiong, Li, Weihua, Xie, Qiang, Hou, Yuxi, Zhan, Shaopeng, Yang, Xi, Xu, Xiaofeng, Cai, Jun, Huang, Zhengrong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4065655/
https://www.ncbi.nlm.nih.gov/pubmed/24995341
http://dx.doi.org/10.1155/2014/376570
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author Zhou, Jieqiong
Li, Weihua
Xie, Qiang
Hou, Yuxi
Zhan, Shaopeng
Yang, Xi
Xu, Xiaofeng
Cai, Jun
Huang, Zhengrong
author_facet Zhou, Jieqiong
Li, Weihua
Xie, Qiang
Hou, Yuxi
Zhan, Shaopeng
Yang, Xi
Xu, Xiaofeng
Cai, Jun
Huang, Zhengrong
author_sort Zhou, Jieqiong
collection PubMed
description The aim of this study was to investigate the effects of simvastatin on insulin secretion in mouse MIN6 cells and the possible mechanism. MIN6 cells were, respectively, treated with 0 μM, 2 μM, 5 μM, and 10 μM simvastatin for 48 h. Radio immunoassay was performed to measure the effect of simvastatin on insulin secretion in MIN6 cells. Luciferase method was used to examine the content of ATP in MIN6 cells. Real-time PCR and western blotting were performed to measure the mRNA and protein levels of inward rectifier potassium channel 6.2 (Kir6.2), voltage-dependent calcium channel 1.2 (Ca(v)1.2), and glucose transporter-2 (GLUT2), respectively. ATP-sensitive potassium current and L-type calcium current were recorded by whole-cell patch-clamp technique. The results showed that high concentrations of simvastatin (5 μM and 10 μM) significantly reduced the synthesis and secretion of insulin compared to control groups in MIN6 cells (P < 0.05). ATP content in simvastatin-treated cells was lower than in control cells (P < 0.05). Compared with control group, the mRNA and protein expression of Kir6.2 increased with treatment of simvastatin (P < 0.05), and mRNA and protein expression of Ca(v)1.2 and GLUT2 decreased in response to simvastatin (P < 0.05). Moreover, simvastatin increased the ATP-sensitive potassium current and reduced the L-type calcium current. These results suggest that simvastatin inhibits the synthesis and secretion of insulin through a reduction in saccharometabolism in MIN6 cells.
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spelling pubmed-40656552014-07-03 Effects of Simvastatin on Glucose Metabolism in Mouse MIN6 Cells Zhou, Jieqiong Li, Weihua Xie, Qiang Hou, Yuxi Zhan, Shaopeng Yang, Xi Xu, Xiaofeng Cai, Jun Huang, Zhengrong J Diabetes Res Research Article The aim of this study was to investigate the effects of simvastatin on insulin secretion in mouse MIN6 cells and the possible mechanism. MIN6 cells were, respectively, treated with 0 μM, 2 μM, 5 μM, and 10 μM simvastatin for 48 h. Radio immunoassay was performed to measure the effect of simvastatin on insulin secretion in MIN6 cells. Luciferase method was used to examine the content of ATP in MIN6 cells. Real-time PCR and western blotting were performed to measure the mRNA and protein levels of inward rectifier potassium channel 6.2 (Kir6.2), voltage-dependent calcium channel 1.2 (Ca(v)1.2), and glucose transporter-2 (GLUT2), respectively. ATP-sensitive potassium current and L-type calcium current were recorded by whole-cell patch-clamp technique. The results showed that high concentrations of simvastatin (5 μM and 10 μM) significantly reduced the synthesis and secretion of insulin compared to control groups in MIN6 cells (P < 0.05). ATP content in simvastatin-treated cells was lower than in control cells (P < 0.05). Compared with control group, the mRNA and protein expression of Kir6.2 increased with treatment of simvastatin (P < 0.05), and mRNA and protein expression of Ca(v)1.2 and GLUT2 decreased in response to simvastatin (P < 0.05). Moreover, simvastatin increased the ATP-sensitive potassium current and reduced the L-type calcium current. These results suggest that simvastatin inhibits the synthesis and secretion of insulin through a reduction in saccharometabolism in MIN6 cells. Hindawi Publishing Corporation 2014 2014-06-04 /pmc/articles/PMC4065655/ /pubmed/24995341 http://dx.doi.org/10.1155/2014/376570 Text en Copyright © 2014 Jieqiong Zhou et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Zhou, Jieqiong
Li, Weihua
Xie, Qiang
Hou, Yuxi
Zhan, Shaopeng
Yang, Xi
Xu, Xiaofeng
Cai, Jun
Huang, Zhengrong
Effects of Simvastatin on Glucose Metabolism in Mouse MIN6 Cells
title Effects of Simvastatin on Glucose Metabolism in Mouse MIN6 Cells
title_full Effects of Simvastatin on Glucose Metabolism in Mouse MIN6 Cells
title_fullStr Effects of Simvastatin on Glucose Metabolism in Mouse MIN6 Cells
title_full_unstemmed Effects of Simvastatin on Glucose Metabolism in Mouse MIN6 Cells
title_short Effects of Simvastatin on Glucose Metabolism in Mouse MIN6 Cells
title_sort effects of simvastatin on glucose metabolism in mouse min6 cells
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4065655/
https://www.ncbi.nlm.nih.gov/pubmed/24995341
http://dx.doi.org/10.1155/2014/376570
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