Intermittent High Glucose Enhances Apoptosis in INS-1 Cells

Joint Authors

Shi, Xiao-li
Ren, Yue-zhong
Wu, Jing

Source

Experimental Diabetes Research

Issue

Vol. 2011, Issue 2011 (31 Dec. 2011), pp.1-7, 7 p.

Publisher

Hindawi Publishing Corporation

Publication Date

2011-06-21

Country of Publication

Egypt

No. of Pages

7

Main Subjects

Diseases

Abstract EN

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.

American Psychological Association (APA)

Shi, Xiao-li& Ren, Yue-zhong& Wu, Jing. 2011. Intermittent High Glucose Enhances Apoptosis in INS-1 Cells. Experimental Diabetes Research،Vol. 2011, no. 2011, pp.1-7.
https://search.emarefa.net/detail/BIM-496177

Modern Language Association (MLA)

Shi, Xiao-li…[et al.]. Intermittent High Glucose Enhances Apoptosis in INS-1 Cells. Experimental Diabetes Research No. 2011 (2011), pp.1-7.
https://search.emarefa.net/detail/BIM-496177

American Medical Association (AMA)

Shi, Xiao-li& Ren, Yue-zhong& Wu, Jing. Intermittent High Glucose Enhances Apoptosis in INS-1 Cells. Experimental Diabetes Research. 2011. Vol. 2011, no. 2011, pp.1-7.
https://search.emarefa.net/detail/BIM-496177

Data Type

Journal Articles

Language

English

Notes

Includes bibliographical references

Record ID

BIM-496177