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

<h4>Aims</h4>To determine the effects of niacin on adiponectin and markers of adipose tissue inflammation in a mouse model of obesity.<h4>Materials and methods</h4>Male C57BL/6 mice were placed on a control or high-fat diet (HFD) and were maintained on such diets for the dura...

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Autores principales: Desiree Wanders, Emily C Graff, B Douglas White, Robert L Judd
Formato: article
Lenguaje:EN
Publicado: Public Library of Science (PLoS) 2013
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Acceso en línea:https://doaj.org/article/11fb98ce65cd48cbb70f19e7da656cda
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Sumario:<h4>Aims</h4>To determine the effects of niacin on adiponectin and markers of adipose tissue inflammation in a mouse model of obesity.<h4>Materials and methods</h4>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.<h4>Results</h4>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.<h4>Conclusions</h4>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.