The Absence of Adiponectin Alters Niacin’s Effects on Adipose Tissue Inflammation in Mice

Obesity is an immunometabolic disease associated with chronic inflammation and the dysregulation of pro- and anti-inflammatory cytokines. One hallmark of obesity is reduced concentrations of the anti-inflammatory adipokine, adiponectin. Pharmacologic doses of niacin produce multiple metabolic benefi...

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Main Authors: Emily C. Graff, Han Fang, Desiree Wanders, Robert L. Judd
Format: Article
Language:English
Published: MDPI AG 2020-08-01
Series:Nutrients
Subjects:
Online Access:https://www.mdpi.com/2072-6643/12/8/2427
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author Emily C. Graff
Han Fang
Desiree Wanders
Robert L. Judd
author_facet Emily C. Graff
Han Fang
Desiree Wanders
Robert L. Judd
author_sort Emily C. Graff
collection DOAJ
description Obesity is an immunometabolic disease associated with chronic inflammation and the dysregulation of pro- and anti-inflammatory cytokines. One hallmark of obesity is reduced concentrations of the anti-inflammatory adipokine, adiponectin. Pharmacologic doses of niacin produce multiple metabolic benefits, including attenuating high-fat diet (HFD)-induced adipose tissue inflammation and increasing adiponectin concentrations. To determine if adiponectin mediates the anti-inflammatory effects of niacin, male C57BL/6J (WT) and adiponectin null (<i>Adipoq</i><sup>-/-</sup>) mice were maintained on a low-fat diet (LFD) or HFD for 6 weeks, before being administered either vehicle or niacin (360 mg/kg/day) for 5 weeks. HFD-fed mice had increased expression of genes associated with macrophage recruitment (<i>Ccl2</i>) and number (<i>Cd68</i>), and increased crown-like structure (CLS) number in adipose tissue. While niacin attenuated <i>Ccl2</i> expression, there were no effects on <i>Cd68</i> or CLS number. The absence of adiponectin did not hinder the ability of niacin to reduce <i>Ccl2</i> expression. HFD feeding increased gene expression of inflammatory markers in the adipose tissue of WT and <i>Adipoq<sup>-/-</sup></i> mice. While niacin tended to decrease the expression of inflammatory markers in WT mice, niacin increased their expression in HFD-fed <i>Adipoq<sup>-/-</sup></i> mice. Therefore, our results indicate that the absence of adiponectin alters the effects of niacin on markers of adipose tissue inflammation in HFD-fed mice, suggesting that the effects of niacin on tissue cytokines may involve adiponectin.
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spelling doaj.art-b3fd27441ea84e3da8450fb6a452edbf2023-11-20T10:00:06ZengMDPI AGNutrients2072-66432020-08-01128242710.3390/nu12082427The Absence of Adiponectin Alters Niacin’s Effects on Adipose Tissue Inflammation in MiceEmily C. Graff0Han Fang1Desiree Wanders2Robert L. Judd3Department of Pathobiology, Auburn University, Auburn, AL 36849, USAPennington Biomedical Research Center, Louisiana State University, Baton Rouge, LA 70808, USADepartment of Nutrition, Georgia State University, Atlanta, GA 30302, USADepartment of Anatomy, Physiology and Pharmacology, Auburn University, Auburn, AL 36849, USAObesity is an immunometabolic disease associated with chronic inflammation and the dysregulation of pro- and anti-inflammatory cytokines. One hallmark of obesity is reduced concentrations of the anti-inflammatory adipokine, adiponectin. Pharmacologic doses of niacin produce multiple metabolic benefits, including attenuating high-fat diet (HFD)-induced adipose tissue inflammation and increasing adiponectin concentrations. To determine if adiponectin mediates the anti-inflammatory effects of niacin, male C57BL/6J (WT) and adiponectin null (<i>Adipoq</i><sup>-/-</sup>) mice were maintained on a low-fat diet (LFD) or HFD for 6 weeks, before being administered either vehicle or niacin (360 mg/kg/day) for 5 weeks. HFD-fed mice had increased expression of genes associated with macrophage recruitment (<i>Ccl2</i>) and number (<i>Cd68</i>), and increased crown-like structure (CLS) number in adipose tissue. While niacin attenuated <i>Ccl2</i> expression, there were no effects on <i>Cd68</i> or CLS number. The absence of adiponectin did not hinder the ability of niacin to reduce <i>Ccl2</i> expression. HFD feeding increased gene expression of inflammatory markers in the adipose tissue of WT and <i>Adipoq<sup>-/-</sup></i> mice. While niacin tended to decrease the expression of inflammatory markers in WT mice, niacin increased their expression in HFD-fed <i>Adipoq<sup>-/-</sup></i> mice. Therefore, our results indicate that the absence of adiponectin alters the effects of niacin on markers of adipose tissue inflammation in HFD-fed mice, suggesting that the effects of niacin on tissue cytokines may involve adiponectin.https://www.mdpi.com/2072-6643/12/8/2427obesityinflammationimmuneniacinadipokines
spellingShingle Emily C. Graff
Han Fang
Desiree Wanders
Robert L. Judd
The Absence of Adiponectin Alters Niacin’s Effects on Adipose Tissue Inflammation in Mice
Nutrients
obesity
inflammation
immune
niacin
adipokines
title The Absence of Adiponectin Alters Niacin’s Effects on Adipose Tissue Inflammation in Mice
title_full The Absence of Adiponectin Alters Niacin’s Effects on Adipose Tissue Inflammation in Mice
title_fullStr The Absence of Adiponectin Alters Niacin’s Effects on Adipose Tissue Inflammation in Mice
title_full_unstemmed The Absence of Adiponectin Alters Niacin’s Effects on Adipose Tissue Inflammation in Mice
title_short The Absence of Adiponectin Alters Niacin’s Effects on Adipose Tissue Inflammation in Mice
title_sort absence of adiponectin alters niacin s effects on adipose tissue inflammation in mice
topic obesity
inflammation
immune
niacin
adipokines
url https://www.mdpi.com/2072-6643/12/8/2427
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