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Differences in the central anorectic effects of glucagon-like peptide-1 and exendin-4 in rats.

Publication ,  Journal Article
Barrera, JG; D'Alessio, DA; Drucker, DJ; Woods, SC; Seeley, RJ
Published in: Diabetes
December 2009

OBJECTIVE: Glucagon-like peptide (GLP)-1 is a regulatory peptide synthesized in the gut and the brain that plays an important role in the regulation of food intake. Both GLP-1 and exendin (Ex)-4, a long-acting GLP-1 receptor (GLP-1r) agonist, reduce food intake when administered intracerebroventricularly, whereas Ex4 is much more potent at suppressing food intake when given peripherally. It has generally been hypothesized that this difference is due to the relative pharmacokinetic profiles of GLP-1 and Ex4, but it is possible that the two peptides control feeding via distinct mechanisms. RESEARCH DESIGN AND METHODS: In this study, the anorectic effects of intracerebroventricular GLP-1 and Ex4, and the sensitivity of these effects to GLP-1r antagonism, were compared in rats. In addition, the GLP-1r dependence of the anorectic effect of intracerebroventricular Ex4 was assessed in GLP-1r(-/-) mice. RESULTS: Intracerebroventricular Ex4 was 100-fold more potent than GLP-1 at reducing food intake, and this effect was insensitive to GLP-1r antagonism. However, GLP-1r antagonists completely blocked the anorectic effect of intraperitoneal Ex4. Despite the insensitivity of intracerebroventricular Ex4 to GLP-1r antagonism, intracerebroventricular Ex4 failed to reduce food intake in GLP-1r(-/-) mice. CONCLUSIONS: These data suggest that although GLP-1rs are required for the actions of Ex4, there appear to be key differences in how GLP-1 and Ex4 interact with central nervous system GLP-1r and in how Ex4 interacts with GLP-1r in the brain versus the periphery. A better understanding of these unique differences may lead to expansion and/or improvement of GLP-1-based therapies for type 2 diabetes and obesity.

Duke Scholars

Published In

Diabetes

DOI

EISSN

1939-327X

Publication Date

December 2009

Volume

58

Issue

12

Start / End Page

2820 / 2827

Location

United States

Related Subject Headings

  • Venoms
  • Rats, Long-Evans
  • Rats
  • Proto-Oncogene Proteins c-fos
  • Peptides
  • Mice, Inbred C57BL
  • Mice
  • Injections, Intraventricular
  • Injections, Intraperitoneal
  • Immunohistochemistry
 

Citation

APA
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ICMJE
MLA
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Barrera, J. G., D’Alessio, D. A., Drucker, D. J., Woods, S. C., & Seeley, R. J. (2009). Differences in the central anorectic effects of glucagon-like peptide-1 and exendin-4 in rats. Diabetes, 58(12), 2820–2827. https://doi.org/10.2337/db09-0281
Barrera, Jason G., David A. D’Alessio, Daniel J. Drucker, Stephen C. Woods, and Randy J. Seeley. “Differences in the central anorectic effects of glucagon-like peptide-1 and exendin-4 in rats.Diabetes 58, no. 12 (December 2009): 2820–27. https://doi.org/10.2337/db09-0281.
Barrera JG, D’Alessio DA, Drucker DJ, Woods SC, Seeley RJ. Differences in the central anorectic effects of glucagon-like peptide-1 and exendin-4 in rats. Diabetes. 2009 Dec;58(12):2820–7.
Barrera, Jason G., et al. “Differences in the central anorectic effects of glucagon-like peptide-1 and exendin-4 in rats.Diabetes, vol. 58, no. 12, Dec. 2009, pp. 2820–27. Pubmed, doi:10.2337/db09-0281.
Barrera JG, D’Alessio DA, Drucker DJ, Woods SC, Seeley RJ. Differences in the central anorectic effects of glucagon-like peptide-1 and exendin-4 in rats. Diabetes. 2009 Dec;58(12):2820–2827.

Published In

Diabetes

DOI

EISSN

1939-327X

Publication Date

December 2009

Volume

58

Issue

12

Start / End Page

2820 / 2827

Location

United States

Related Subject Headings

  • Venoms
  • Rats, Long-Evans
  • Rats
  • Proto-Oncogene Proteins c-fos
  • Peptides
  • Mice, Inbred C57BL
  • Mice
  • Injections, Intraventricular
  • Injections, Intraperitoneal
  • Immunohistochemistry