4.7 Article

1,25-Dihydroxyvitamin D3 protects obese rats from metabolic syndrome via promoting regulatory T cell-mediated resolution of inflammation

期刊

ACTA PHARMACEUTICA SINICA B
卷 8, 期 2, 页码 178-187

出版社

INST MATERIA MEDICA, CHINESE ACAD MEDICAL SCIENCES
DOI: 10.1016/j.apsb.2018.01.001

关键词

Insulin resistance; Dyslipidemia; MSG-obese rat; Treg cell; Vitamin D-3; 1,25-Dihydroxyvitamin D-3

资金

  1. National Natural Science Foundation of China [81773800, 81471070]
  2. CAMS Innovation Fund for Medical Sciences (CIFMS) [2016-I2M-1-010, 2016-I2M-1-012]

向作者/读者索取更多资源

Vitamin D-3 has been found to produce therapeutic effects on obesity-associated insulin resistance and dyslipidemia through its potent anti-inflammatory activity, but the precise immunomodulatory mechanism remains poorly understood. In the present study we found that 1,25-dihydroxyvitamin D-3 [1,25(OH)(2)D-3], the biologically active form of vitamin D-3, significantly attenuated monosodium glutamate (MSG)-induced obesity and insulin resistance as indicated by body weight reduction, oral glucose tolerance improvement, and a glucose infusion rate increase as detected with hyperinsulinemiceuglycemic clamp. Moreover, 1,25(OH)(2)D-3 not only restored pancreatic islet functions but also improved lipid metabolism in insulin-targeted tissues. The protective effects of 1,25(OH)(2)D-3 on glycolipid metabolism were attributed to its ability to inhibit an obesity-activated inflammatory response in insulin secretory and targeted tissues, as indicated by reduced infiltration of macrophages in pancreas islets and adipose tissue while enhancing the expression of Tgf-beta 1 in liver tissue, which was accompanied by increased infiltration of Treg cells in immune organs such as spleen and lymph node as well as in insulin targeted tissues such as liver, adipose, and muscle. Together, our findings suggest that 1,25(OH)(2)D-3 serves as a beneficial immunomodulator for the prevention and treatment of obesity or metabolic syndrome through its anti-inflammatory effects. (C) 2018 Chinese Pharmaceutical Association and Institute of Materia Medica, Chinese Academy of Medical Sciences. Production and hosting by Elsevier B.V.

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