Alleviation of Hyperglycemia Induced Vascular Endothelial Injury by Exenatide Might Be Related to the Reduction of Nitrooxidative Stress

• Published in: BioMed research international 2013-01, Vol.2013 (2013), p.1-11
• Main Authors: Wang, Wen, Wang, Yun, Zhang, Mei, Huang, Wen, Xiong, Hai-yan, Xu, Chun-ling, Zhao, Qian, Wang, Si-yu
• Format: Article
• Language: English
• Subjects: Animals; Aorta, Thoracic - drug effects; Aorta, Thoracic - pathology; Cardiovascular Abnormalities - complications; Cardiovascular Abnormalities - drug therapy; Cardiovascular Abnormalities - pathology; Diabetes Mellitus, Experimental - complications; Diabetes Mellitus, Experimental - drug therapy; Diabetes Mellitus, Experimental - metabolism; Endothelium, Vascular - drug effects; Endothelium, Vascular - injuries; Hyperglycemia - complications; Hyperglycemia - drug therapy; Hyperglycemia - metabolism; Male; Nitric Oxide - metabolism; Nitric Oxide Synthase Type II - metabolism; Oxidative Stress - drug effects; Peptides - administration & dosage; Rats; Venoms - administration & dosage
• ISSN: 2314-6133; 2314-6141
• DOI: 10.1155/2013/843657

We will investigate the effects of exenatide on vascular endothelial injury and nitrooxidative stress in hyperglycemia both in vivo and in vitro and explore the role of nitrooxidative stress in endothelium-protective action of exenatide. Healthy male Wistar rats were randomly divided into 4 groups: control, diabetes mellitus (DM) model, low dose of exenatide treatment, and high doseof exenatide treatment. In vitro study showed that, compared with control group, the DM rats exhibited a lowered endothelium-dependent relaxation and damaged structural integrity of thoracic aortas, and there was a significant increase in plasma nitrotyrosine concentration. These parameters were improved after treatment with either low dose or high dose of exenatide for 45 days. In vitro study showed that exendin-4 (the active ingredient of exenatide) attenuated HUVECs injury induced by high glucose, with improving cell viability and attenuating cell apoptosis. Exendin-4 also significantly alleviated the increased malondialdehyde (MDA), nitrotyrosine content, and inducible nitric oxide synthase (iNOS) expression induced by high glucose in HUVECs. In conclusion, this study demonstrates that exenatide treatment can alleviate the vascular endothelial injury, as well as attenuating the nitrooxidative stress in hyperglycemia, implying that the endothelium-protective effect of exenatide might be related to the reduction of nitrooxidative stress.