Myeloperoxidase deletion prevents high-fat diet-induced obesity and insulin resistance

• Published in: Diabetes (New York, N.Y.) Vol. 63; no. 12; pp. 4172 - 4185
• Main Authors: Wang, Qilong, Xie, Zhonglin, Zhang, Wencheng, Zhou, Jun, Wu, Yue, Zhang, Miao, Zhu, Huaiping, Zou, Ming-Hui
• Format: Journal Article
• Language: English
• Published: United States American Diabetes Association 01-12-2014
• Subjects: Adipose Tissue - immunology; Adipose Tissue, Brown - immunology; Adipose Tissue, Brown - metabolism; Animals; Body Temperature Regulation - physiology; Cell Count; Cytokines; Diet, High-Fat - adverse effects; Glucose Tolerance Test; Inflammation - immunology; Insulin resistance; Insulin Resistance - genetics; Insulin Resistance - immunology; Ion Channels - metabolism; Macrophages - cytology; Macrophages - immunology; Mice; Mice, Knockout; Mitochondria - metabolism; Mitochondrial Proteins - metabolism; Neutrophils - cytology; Neutrophils - immunology; Obesity; Obesity - enzymology; Obesity - genetics; Obesity - immunology; Obesity Studies; Oxygen; Oxygen Consumption; Peroxidase - genetics; Peroxidase - immunology; Peroxidase - metabolism; Protein expression; Rodents; Uncoupling Protein 1; Up-Regulation
• ISSN: 0012-1797; 1939-327X
• DOI: 10.2337/db14-0026

Activation of myeloperoxidase (MPO), a heme protein primarily expressed in granules of neutrophils, is associated with the development of obesity. However, whether MPO mediates high-fat diet (HFD)-induced obesity and obesity-associated insulin resistance remains to be determined. Here, we found that consumption of an HFD resulted in neutrophil infiltration and enhanced MPO expression and activity in epididymal white adipose tissue, with an increase in body weight gain and impaired insulin signaling. MPO knockout (MPO(-/-)) mice were protected from HFD-enhanced body weight gain and insulin resistance. The MPO inhibitor 4-aminobenzoic acid hydrazide reduced peroxidase activity of neutrophils and prevented HFD-enhanced insulin resistance. MPO deficiency caused high body temperature via upregulation of uncoupling protein-1 and mitochondrial oxygen consumption in brown adipose tissue. Lack of MPO also attenuated HFD-induced macrophage infiltration and expression of proinflammatory cytokines. We conclude that activation of MPO in adipose tissue contributes to the development of obesity and obesity-associated insulin resistance. Inhibition of MPO may be a potential strategy for prevention and treatment of obesity and insulin resistance.