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Intermittent High Glucose Enhances Apoptosis in INS-1 Cells
To investigate the effect of intermittent high glucose (IHG) and sustained high glucose (SHG) on inducing β-cell apoptosis and the potential involved mechanisms, INS-1 beta cells were incubated for 72 h in the medium containing different glucose concentrations: control (5.5 mmol/L), SHG (33.3 mmol/L...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3124292/ https://www.ncbi.nlm.nih.gov/pubmed/21747833 http://dx.doi.org/10.1155/2011/754673 |
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author | Shi, Xiao-li Ren, Yue-zhong Wu, Jing |
author_facet | Shi, Xiao-li Ren, Yue-zhong Wu, Jing |
author_sort | Shi, Xiao-li |
collection | PubMed |
description | To investigate the effect of intermittent high glucose (IHG) and sustained high glucose (SHG) on inducing β-cell apoptosis and the potential involved mechanisms, INS-1 beta cells were incubated for 72 h in the medium containing different glucose concentrations: control (5.5 mmol/L), SHG (33.3 mmol/L), and IHG (5.5 mmol/L and 33.3 mmol/L glucose alternating every 12 h). Cell viability, apoptosis rate, and oxidative-stress markers were determined. The results showed that the apoptosis induced by IHG was more obvious than that by SHG. Simultaneously, the intracellular level of oxidative stress was more significantly increased in INS-1 cells exposed to IHG. These findings suggest that intermittent high glucose could be more deleterious to β-cell than a constant high concentration of glucose, this may be due to the aggravation of oxidative stress triggered by intermittent high glucose. |
format | Online Article Text |
id | pubmed-3124292 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-31242922011-07-11 Intermittent High Glucose Enhances Apoptosis in INS-1 Cells Shi, Xiao-li Ren, Yue-zhong Wu, Jing Exp Diabetes Res Research Article To investigate the effect of intermittent high glucose (IHG) and sustained high glucose (SHG) on inducing β-cell apoptosis and the potential involved mechanisms, INS-1 beta cells were incubated for 72 h in the medium containing different glucose concentrations: control (5.5 mmol/L), SHG (33.3 mmol/L), and IHG (5.5 mmol/L and 33.3 mmol/L glucose alternating every 12 h). Cell viability, apoptosis rate, and oxidative-stress markers were determined. The results showed that the apoptosis induced by IHG was more obvious than that by SHG. Simultaneously, the intracellular level of oxidative stress was more significantly increased in INS-1 cells exposed to IHG. These findings suggest that intermittent high glucose could be more deleterious to β-cell than a constant high concentration of glucose, this may be due to the aggravation of oxidative stress triggered by intermittent high glucose. Hindawi Publishing Corporation 2011 2011-06-21 /pmc/articles/PMC3124292/ /pubmed/21747833 http://dx.doi.org/10.1155/2011/754673 Text en Copyright © 2011 Xiao-li Shi 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 Shi, Xiao-li Ren, Yue-zhong Wu, Jing Intermittent High Glucose Enhances Apoptosis in INS-1 Cells |
title | Intermittent High Glucose Enhances Apoptosis in INS-1 Cells |
title_full | Intermittent High Glucose Enhances Apoptosis in INS-1 Cells |
title_fullStr | Intermittent High Glucose Enhances Apoptosis in INS-1 Cells |
title_full_unstemmed | Intermittent High Glucose Enhances Apoptosis in INS-1 Cells |
title_short | Intermittent High Glucose Enhances Apoptosis in INS-1 Cells |
title_sort | intermittent high glucose enhances apoptosis in ins-1 cells |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3124292/ https://www.ncbi.nlm.nih.gov/pubmed/21747833 http://dx.doi.org/10.1155/2011/754673 |
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