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Decreased hepatic gluconeogenesis in transgenic rats with increased circulating angiotensin-(1-7)

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Item Type:Article
Title:Decreased hepatic gluconeogenesis in transgenic rats with increased circulating angiotensin-(1-7)
Creators Name:Bilman, V. and Mares-Guia, L. and Nadu, A.P. and Bader, M. and Campagnole-Santos, M.J. and Santos, R.A.S. and Santos, S.H.S.
Abstract:The renin-angiotensin (Ang) system (RAS) plays an important role in the control of glucose metabolism and glycemia. Several studies demonstrated that the effects of angiotensin-(1-7) are mainly opposite to the actions of biological angiotensin II. Recent studies have demonstrated that rats with increased circulating angiotensin-(1-7), acting through the G protein coupled receptor Mas, have enhanced glucose tolerance and insulin sensitivity, presenting improved metabolic parameters. However, there is no data regarding the role of angiotensin-(1-7)-Mas axis in hepatic glycemic metabolism. In the present study, the gluconeogenesis and glycogenolysis was investigated in Sprague-Dawley (SD) and in TGR(A1-7)3292 (TGR) rats which present approximately twofold increase in plasma Ang-(1-7) levels compared to SD. The pyruvate administration in fasted rats showed a decreased synthesis of glucose in TGR compared to the SD rats, pointing to a downregulation of gluconeogenesis. Supporting this data, the mRNA evaluation of gluconeogenic enzymes showed a significant reduction in phosphoenolpyruvate carboxykinase reinforced by a significantly diminished expression of hepatocyte nuclear factor 4{alpha} (HNF-4{alpha}), responsible for the regulation of gluconeogenic enzymes. In conclusion our data show that the improved glucose metabolism induced by Ang-(1-7) could be due, at least in part, to a downregulation of hepatic gluconeogenesis.
Keywords:Angiotensin I, Gluconeogenesis, Liver, Peptide Fragments, Animals, Rats
Source:Peptides
ISSN:0196-9781
Publisher:Elsevier (U.S.A.)
Volume:37
Number:2
Page Range:247-251
Date:October 2012
Official Publication:https://doi.org/10.1016/j.peptides.2012.08.002
PubMed:View item in PubMed

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