Chronic endothelin-1 infusion causes adipocyte hyperplasia in rats

Obesity (Silver Spring). 2016 Mar;24(3):643-53. doi: 10.1002/oby.21394. Epub 2016 Feb 1.

Abstract

Objective: The aim of this study was to investigate the regulatory mechanism of endothelin-1 (ET-1), an endothelium-derived vasoconstrictor, on adipogenesis in vitro and in vivo.

Methods: 3T3-L1 preadipocytes were used to explore the mechanisms mediating ET-1 actions on preadipocyte proliferation and adipocyte differentiation. To investigate the in vivo effect of ET-1, male Sprague-Dawley rats were infused with ET-1 or saline for 4 weeks via intraperitoneally implanted osmotic pumps, and the fat pad weight and adipocyte size of adipose tissues were measured.

Results: ET-1 stimulated preadipocyte proliferation and increased the cell number at the mitotic clonal expansion stage of adipocyte differentiation via the endothelin A receptor (ETAR) and activation of the protein kinase C (PKC) pathway. ET-1, via ETAR, inhibited adipocyte differentiation partially through an ERK-dependent pathway. Furthermore, no significant difference in the body weight and fat pad weight was observed in either ET-1- or saline-infused rats. Compared with saline-infused rats, the adipocyte cell number was significantly increased but the adipocyte size was significantly decreased in ET-1-infused rats.

Conclusions: Chronic ET-1 infusion increased the number of small adipocytes without the change of white adipose tissue mass in rats, which were associated with ET-1-stimulated preadipocyte proliferation, but not ET-1-suppressed adipocyte differentiation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 3T3-L1 Cells / drug effects
  • Adipocytes / drug effects*
  • Adipocytes / metabolism
  • Adipogenesis / drug effects
  • Adipose Tissue / metabolism
  • Animals
  • Body Weight / drug effects
  • Cell Differentiation / drug effects*
  • Dose-Response Relationship, Drug
  • Endothelin-1 / metabolism
  • Endothelin-1 / pharmacology*
  • Hyperplasia / etiology*
  • Hyperplasia / metabolism
  • Male
  • Mice
  • Obesity / metabolism
  • Rats
  • Rats, Sprague-Dawley
  • Receptor, Endothelin A / drug effects*
  • Receptor, Endothelin A / metabolism

Substances

  • Endothelin-1
  • Receptor, Endothelin A