4.7 Article

Metformin directly inhibits ghrelin secretion through AMP-activated protein kinase in rat primary gastric cells

Journal

DIABETES OBESITY & METABOLISM
Volume 15, Issue 3, Pages 276-279

Publisher

WILEY-BLACKWELL
DOI: 10.1111/dom.12021

Keywords

antidiabetic drug; appetite control; biguanides; cellular pharmacology; drug mechanism; metformin

Funding

  1. Canadian Institutes of Health Research [MOP-82795]
  2. Canada foundation for innovation
  3. IWK Research Foundation
  4. Natural Sciences and Engineering Research Council
  5. Nova Scotia Heart and Stroke foundation
  6. Atlee Fund, Department of Obstetrics and Gynecology, Dalhousie University

Ask authors/readers for more resources

The antidiabetic drug Metformin causes weight loss in both diabetic and non-diabetic individuals. Metformin treatment is also associated with lower circulating levels of the orexigenic hormone ghrelin. To test whether Metformin directly affects ghrelin cells, rat primary stomach cells were treated with Metformin and the levels of ghrelin secretion, proghrelin gene expression and activation of adenosine monophosphate-activated protein kinase (AMPK) were examined. Metformin significantly reduced ghrelin secretion and proghrelin mRNA production and both these effects were blocked by co-incubation with the AMPK inhibitor compound C. Furthermore, the AMPK activator 5-amino-1-beta-D-ribofuranosyl-imidazole-4-carboxamide (AICAR) significantly inhibited ghrelin secretion. Additionally, ghrelin cells were shown to express AMPK. Finally, Metformin treatment caused a significant increase in the level of phosphorylated (active) AMPK. Our results show that Metformin directly inhibits stomach ghrelin production and secretion through AMPK. This reduction in ghrelin secretion may be one of the key components in Metformin's mechanism of weight loss.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.7
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available