Niacin increases adiponectin and decreases adipose tissue inflammation in high fat diet-fed mice

PLoS One. 2013 Aug 13;8(8):e71285. doi: 10.1371/journal.pone.0071285. eCollection 2013.

Abstract

Aims: To determine the effects of niacin on adiponectin and markers of adipose tissue inflammation in a mouse model of obesity.

Materials and methods: Male C57BL/6 mice were placed on a control or high-fat diet (HFD) and were maintained on such diets for the duration of the study. After 6 weeks on the control or high fat diets, vehicle or niacin treatments were initiated and maintained for 5 weeks. Identical studies were conducted concurrently in HCA2 (-/-) (niacin receptor(-/-)) mice.

Results: Niacin increased serum concentrations of the anti-inflammatory adipokine, adiponectin by 21% in HFD-fed wild-type mice, but had no effect on lean wild-type or lean or HFD-fed HCA2 (-/-) mice. Niacin increased adiponectin gene and protein expression in the HFD-fed wild-type mice only. The increases in adiponectin serum concentrations, gene and protein expression occurred independently of changes in expression of PPARγ C/EBPα or SREBP-1c (key transcription factors known to positively regulate adiponectin gene transcription) in the adipose tissue. Further, niacin had no effect on adipose tissue expression of ERp44, Ero1-Lα, or DsbA-L (key ER chaperones involved in adiponectin production and secretion). However, niacin treatment attenuated HFD-induced increases in adipose tissue gene expression of MCP-1 and IL-1β in the wild-type HFD-fed mice. Niacin also reduced the expression of the pro-inflammatory M1 macrophage marker CD11c in HFD-fed wild-type mice.

Conclusions: Niacin treatment attenuates obesity-induced adipose tissue inflammation through increased adiponectin and anti-inflammatory cytokine expression and reduced pro-inflammatory cytokine expression in a niacin receptor-dependent manner.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adiponectin / genetics
  • Adiponectin / metabolism*
  • Adipose Tissue / drug effects
  • Adipose Tissue / metabolism*
  • Animals
  • Diet, High-Fat*
  • Gene Expression Regulation / drug effects
  • Macrophages / metabolism
  • Male
  • Mice
  • Mice, Knockout
  • Molecular Chaperones / genetics
  • Molecular Chaperones / metabolism
  • Niacin / metabolism*
  • Niacin / pharmacology
  • Panniculitis / genetics
  • Panniculitis / metabolism*
  • Transcription Factors / genetics
  • Transcription Factors / metabolism

Substances

  • Adiponectin
  • Molecular Chaperones
  • Transcription Factors
  • Niacin