Angiotensin 1-7 stimulates brown adipose tissue and reduces diet-induced obesity

Am J Physiol Endocrinol Metab. 2018 Feb 1;314(2):E131-E138. doi: 10.1152/ajpendo.00192.2017. Epub 2017 Oct 24.

Abstract

The renin-angiotensin system is a key regulator of metabolism with beneficial effects of the angiotensin 1-7 (Ang 1-7) peptide. We hypothesized that the antiobesity effect of Ang 1-7 was related to the stimulation of brown adipose tissue (BAT). We administered Ang 1-7 (0.54 mg kg-1 day-1) for 28 days via implanted micro-osmotic pumps to mice with high-fat diet (HFD)-induced obesity. Ang 1-7 treatment reduced body weight, upregulated thermogenesis, and ameliorated impaired glucose homeostasis without affecting food consumption. Furthermore, Ang 1-7 treatment enlarged BAT and the increased expression of UCP1, PRDM16, and prohibitin. Alterations in PRDM16 expression correlated with increased AMPK and phosphorylation of mTOR. Ang 1-7 treatment elevated thermogenesis in subcutaneous white adipose tissue without altering UCP1 expression. These changes occurred in the context of decreased lipid accumulation in BAT from HFD-fed mice, preserved insulin signaling concomitant with phosphorylation of hormone-sensitive lipase and decreased expression of perilipin. These data suggest that Ang 1-7 induces brown adipocyte differentiation leading to upregulation of thermogenesis and improved metabolic profile in diet-induced obesity. Enhancing Ang 1-7 action represents a promising therapy to increase BAT and to reduce the metabolic complications associated with diet-induced obesity.

Keywords: Ang 1–7; PRDM16; UCP1; high-fat diet; obesity.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adipocytes, Brown / drug effects
  • Adipocytes, Brown / physiology
  • Adipose Tissue, Brown / drug effects*
  • Adipose Tissue, Brown / metabolism
  • Angiotensin I / pharmacology*
  • Animals
  • Body Weight / drug effects
  • Cell Proliferation / drug effects
  • Diet, High-Fat*
  • Energy Metabolism / drug effects
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Obesity / etiology
  • Obesity / prevention & control*
  • Peptide Fragments / pharmacology*
  • Thermogenesis / drug effects*

Substances

  • Peptide Fragments
  • Angiotensin I
  • angiotensin I (1-7)