Short-Term Caloric Restriction Attenuates Obesity-Induced Pro-Inflammatory Response in Male Rhesus Macaques

Nutrients. 2020 Feb 18;12(2):511. doi: 10.3390/nu12020511.

Abstract

White adipose tissue (WAT) hypertrophy is an essential hallmark of obesity and is associated with the activation of resident immune cells. While the benefits of caloric restriction (CR) on health span are generally accepted, its effects on WAT physiology are not well understood. We previously demonstrated that short-term CR reverses obesity in male rhesus macaques exposed to a high-fat Western-style diet (WSD). Here, we analyzed subcutaneous WAT biopsies collected from this cohort of animals before and after WSD and following CR. This analysis showed that WSD induced adipocyte hypertrophy and inhibited β-adrenergic-simulated lipolysis. CR reversed adipocyte hypertrophy, but WAT remained insensitive to β-adrenergic agonist stimulation. Whole-genome transcriptional analysis revealed that β3-adrenergic receptor and de novo lipogenesis genes were downregulated by WSD and remained downregulated after CR. In contrast, WSD-induced pro-inflammatory gene expression was effectively reversed by CR. Furthermore, peripheral blood monocytes isolated during the CR period exhibited a significant reduction in the production of pro-inflammatory cytokines compared to those obtained after WSD. Collectively, this study demonstrates that short-term CR eliminates an obesity-induced pro-inflammatory response in WAT and peripheral monocytes.

Keywords: adipose tissue; caloric restriction; high-fat diet; nonhuman primates; obesity; transcriptome; western-style diet.

MeSH terms

  • Adipose Tissue, White / metabolism*
  • Adipose Tissue, White / pathology
  • Adrenergic beta-Agonists
  • Animals
  • Caloric Restriction*
  • Cytokines / metabolism*
  • Diet, High-Fat / adverse effects*
  • Down-Regulation
  • Hypertrophy / diet therapy
  • Hypertrophy / etiology
  • Inflammation Mediators / metabolism*
  • Lipogenesis / genetics
  • Lipolysis
  • Macaca mulatta
  • Male
  • Monocytes / metabolism
  • Obesity / diet therapy*
  • Obesity / etiology
  • Obesity / metabolism*
  • Obesity / pathology
  • Receptors, Adrenergic, beta-3 / genetics

Substances

  • Adrenergic beta-Agonists
  • Cytokines
  • Inflammation Mediators
  • Receptors, Adrenergic, beta-3