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2000
Volume 11, Issue 1
  • ISSN: 1573-3998
  • E-ISSN: 1875-6417

Abstract

Pancreatic β-cells secrete insulin when blood glucose levels become high. However, when β-cells are chronically exposed to hyperglycemia, their function gradually deteriorates. Although such phenomena are called as β-cell glucose toxicity, its molecular mechanism remained unclear. This manuscript describes the possible mechanism for such β-cell dysfunction. In the diabetic state, nuclear expression levels of pancreatic transcription factors PDX-1 and MafA are decreased. In addition, incretin receptor expression in β- cells is decreased, which is likely involved in the impairment of incretin effects in diabetes. Taken together, it is likely that down-regulation of pancreatic transcription factors and/or incretin receptors are involved in β-cell dysfunction observed in type 2 diabetes.

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/content/journals/cdr/10.2174/1573399811666141216160217
2015-03-01
2025-05-30
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/content/journals/cdr/10.2174/1573399811666141216160217
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  • Article Type:
    Research Article
Keyword(s): GLP-1 receptor; MafA; Pancreatic β-cells; PDX-1; reactive oxygen species
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