Improved lipid and glucose metabolism in transgenic rats with increased circulating angiotensin-(1-7)

Arterioscler Thromb Vasc Biol. 2010 May;30(5):953-61. doi: 10.1161/ATVBAHA.109.200493. Epub 2010 Mar 4.

Abstract

Objective: Obesity and diabetes remain among the world's most pervasive health problems. Although the importance of angiotensin II for metabolic regulation is well documented, the role of the angiotensin-(1-7)/Mas axis in this process is poorly understood. The aim of this study was to evaluate the effect of increased angiotensin-(1-7) plasma levels in lipid and glucose metabolism using transgenic rats that express an angiotensin-(1-7)-releasing fusion protein, TGR(A1-7)3292 (TGR).

Methods and results: The increased angiotensin-(1-7) levels in TGR induced enhanced glucose tolerance, insulin sensitivity, and insulin-stimulated glucose uptake. In addition, TGR presented decreased triglycerides and cholesterol levels, as well as a significant decrease in abdominal fat mass, despite normal food intake. These alterations were accompanied by a marked decrease of angiotensinogen expression and increased Akt in adipose tissue. Furthermore, augmented plasma levels and expression in adipose tissue was observed for adiponectin. Accordingly, angiotensin-(1-7) stimulation increased adiponectin production by primary adipocyte culture, which was blocked by the Mas antagonist A779. Circulating insulin and muscle glycogen content were not altered in TGR.

Conclusion: These results show that increased circulating angiotensin-(1-7) levels lead to prominent changes in glucose and lipid metabolism.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adipocytes / metabolism
  • Adiponectin / blood
  • Adipose Tissue / cytology
  • Adipose Tissue / drug effects
  • Adipose Tissue / metabolism*
  • Adiposity
  • Angiotensin I
  • Angiotensin II / analogs & derivatives
  • Angiotensin II / blood*
  • Angiotensin II / genetics
  • Angiotensin II / pharmacology
  • Animals
  • Biomarkers / blood
  • Blood Glucose / drug effects
  • Blood Glucose / metabolism*
  • Body Weight
  • Cells, Cultured
  • Cholesterol / blood
  • Insulin / blood
  • Leptin / blood
  • Lipid Metabolism* / drug effects
  • Lipid Metabolism* / genetics
  • Male
  • Peptide Fragments / blood*
  • Peptide Fragments / genetics
  • Peptide Fragments / pharmacology
  • Proto-Oncogene Mas
  • Proto-Oncogene Proteins / antagonists & inhibitors
  • Proto-Oncogene Proteins / metabolism
  • Proto-Oncogene Proteins c-akt / metabolism
  • Rats
  • Rats, Sprague-Dawley
  • Rats, Transgenic
  • Receptors, G-Protein-Coupled / antagonists & inhibitors
  • Receptors, G-Protein-Coupled / metabolism
  • Time Factors
  • Triglycerides / blood
  • Up-Regulation

Substances

  • 7-Ala-angiotensin (1-7)
  • Adiponectin
  • Adipoq protein, rat
  • Biomarkers
  • Blood Glucose
  • Insulin
  • Leptin
  • Peptide Fragments
  • Proto-Oncogene Mas
  • Proto-Oncogene Proteins
  • Receptors, G-Protein-Coupled
  • Triglycerides
  • Angiotensin II
  • Angiotensin I
  • Cholesterol
  • Proto-Oncogene Proteins c-akt
  • angiotensin I (1-7)