Bariatric surgery relieves type 2 diabetes and modulates inflammatory factors and coronary endothelium eNOS/iNOS expression in db/db mice

被引:17
作者
Liu, Bingyang [1 ]
Kuang, Lirun [2 ]
Liu, Jingang [2 ]
机构
[1] China Med Univ, Dept Endocrinol, Shengjing Hosp, Shenyang 110004, Liaoning Provin, Peoples R China
[2] China Med Univ, Dept Gen Surg, Shengjing Hosp, Shenyang 110004, Liaoning Provin, Peoples R China
关键词
bariatric surgery; type 2 diabetes mellitus; obesity; vascular dysfunction; NECROSIS-FACTOR-ALPHA; GASTRIC BYPASS; INSULIN SENSITIVITY; ACYLATED PEPTIDE; WEIGHT-LOSS; LIFE-STYLE; GHRELIN; ADIPONECTIN; PREVALENCE; MECHANISMS;
D O I
10.1139/cjpp-2013-0034
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Overexpression of endothelial nitric oxide synthetase (eNOS)/inducible nitric oxide synthase (iNOS) and inhibition of inflammatory factors can improve vascular function. We hypothesized that bariatric (gastric bypass) surgery could inhibit inflammatory factors and improve the eNOS/iNOS expression of coronary arterioles in the db/db mice. The animals were randomly allocated to the following groups: sham-operated lean mice, lean mice that underwent surgery, sham-operated db/db mice, and db/db mice that underwent surgery (5, 10, 20, and 30 days post-operation). The plasma levels of adiponectin, ghrelin, and IL-6, as well as the protein expression of eNOS/iNOS in coronary arterioles were measured with Western blot. Bariatric surgery decreased body mass and blood glucose levels in db/db mice. Ghrelin receptor and GHS-R1a expression in the hypothalamus were increased in db/db mice, but surgery attenuated GHS-R1a expression. Bariatric surgery elevated plasma concentration and protein expression of adiponectin and ghrelin, and attenuated plasma concentration and protein expression of IL-6. Coronary protein expression of eNOS and SOD2 was lower in the sham-operated db/db mice, and bariatric surgery increased eNOS and SOD2 expression. Gastric bypass surgery upregulates ghrelin and adiponectin expression, and decreases IL-6 expression, which might induce up-regulation of eNOS and SOD2, and down-regulation of iNOS. These interactions could counteract the endothelium dysfunction in type 2 diabetes mellitus.
引用
收藏
页码:70 / 77
页数:8
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