Downregulation of CTRP-3 by Weight Loss In Vivo and by Bile Acids and Incretins in Adipocytes In Vitro

Int J Mol Sci. 2020 Oct 31;21(21):8168. doi: 10.3390/ijms21218168.

Abstract

The adipokine CTRP-3 (C1q/TNF-related protein-3) exerts anti-inflammatory and anti-diabetic effects. Its regulation in obesity and during weight loss is unknown. Serum and adipose tissue (AT) samples were obtained from patients (n = 179) undergoing bariatric surgery (BS). Moreover, patients (n = 131) participating in a low-calorie diet (LCD) program were studied. CTRP 3 levels were quantified by ELISA and mRNA expression was analyzed in AT and in 3T3-L1 adipocytes treated with bile acids and incretins. There was a persistent downregulation of CTRP-3 serum levels during weight loss. CTRP-3 expression was higher in subcutaneous than in visceral AT and serum levels of CTRP-3 were positively related to AT expression levels. A rapid decrease of circulating CTRP-3 was observed immediately upon BS, suggesting weight loss-independent regulatory mechanisms. Adipocytes CTRP-3 expression was inhibited by primary bile acid species and GLP 1. Adipocyte-specific CTRP-3 deficiency increased bile acid receptor expression. Circulating CTRP-3 levels are downregulated during weight loss, with a considerable decline occurring immediately upon BS. Mechanisms dependent and independent of weight loss cause the post-surgical decline of CTRP-3. The data strongly argue for regulatory interrelations of CTRP-3 with bile acids and incretin system.

Keywords: C1q/TNF-related protein-3; bariatric surgery; bile acids; incretins; low calorie diet; obesity.

MeSH terms

  • Adipocytes / drug effects
  • Adipocytes / metabolism*
  • Adipokines / blood
  • Adipokines / genetics
  • Adipokines / metabolism*
  • Adult
  • Animals
  • Bariatric Surgery / methods
  • Bile Acids and Salts / pharmacology*
  • Cells, Cultured
  • Disease Models, Animal
  • Down-Regulation
  • Female
  • Gastrointestinal Agents / pharmacology
  • Glucagon-Like Peptide 1 / pharmacology
  • Humans
  • Incretins / pharmacology*
  • Male
  • Mice
  • Mice, Inbred BALB C
  • Mice, Knockout
  • Obesity / blood
  • Obesity / metabolism*
  • Obesity / pathology
  • Obesity / surgery
  • Tumor Necrosis Factors / blood
  • Tumor Necrosis Factors / genetics
  • Tumor Necrosis Factors / metabolism*
  • Weight Loss*

Substances

  • Adipokines
  • Bile Acids and Salts
  • C1QTNF3 protein, human
  • CORS26 protein, mouse
  • Gastrointestinal Agents
  • Incretins
  • Tumor Necrosis Factors
  • Glucagon-Like Peptide 1