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Glucagon-like peptide-1(1-37) can enhance blood glucose homeostasis in mice

  • Lifen Zhao
  • , Haifeng Ye
  • , Dongqing Li
  • , Xun Lao
  • , Juan Li
  • , Zhenghua Wang
  • , Lei Xiao
  • , Zirong Wu
  • , Jing Huang*
  • *此作品的通讯作者
  • East China Normal University
  • Swiss Federal Institute of Technology Zurich

科研成果: 期刊稿件文章同行评审

摘要

Glucagon-like peptide-1 (GLP-1) is produced by the posttranslational processing of proglucagon and acts as a regulator of various homeostatic events. No blood glucose regulation role of GLP-1(1-37) has previously been identified. However, our findings in this study clearly showed that GLP-1(1-37) could lower blood glucose levels both in normal and diabetic mice. In vitro stability analysis demonstrated that GLP-1(1-37) was more stable than GLP-1(7-37), with 94.7% of the initial amount of peptide left after a 4. h exposure to mouse serum. Moreover, GLP-1(1-37) was confirmed to be a highly potent agonist of the GLP-1 receptor (GLP-1R) by measuring the expression of the luciferase reporter gene expression in transiently transfected human embryonic kidney (HEK293) cells. Unlike the glucose lowering effect of GLP-1(7-37), the glucose-lowering effect of GLP-1(1-37) could not be blocked by the GLP-1R antagonist exendin(9-39), suggesting that GLP-1(1-37) might activate the GLP-1R via a different mechanism. Therefore, our findings suggest that GLP-1(1-37) could be a potential therapeutic drug for the treatment of type 2 diabetes in the future.

源语言英语
页(从-至)1-5
页数5
期刊Regulatory Peptides
178
1-3
DOI
出版状态已出版 - 10 10月 2012

联合国可持续发展目标

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  1. 可持续发展目标 3 - 良好健康与福祉
    可持续发展目标 3 良好健康与福祉

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