Ginsenoside Re inhibits vascular neointimal hyperplasia in balloon-injured carotid arteries through activating the eNOS/NO/cGMP pathway in rats

被引:17
作者
Gao, Yang [1 ]
Gao, Chen-Ying
Zhu, Ping
Xu, Shang-Fu
Luo, Yun-Mei
Deng, Jiang
Yang, Dan-Li
机构
[1] Zunyi Med Univ, Key Lab Basic Pharmacol, Minist Educ, Zunyi 563003, Guizhou, Peoples R China
基金
中国国家自然科学基金;
关键词
Ginsenoside Re; Neointimal hyperplasia; Balloon injury; Nitric oxide; Endothelial nitric oxide synthase; ENDOTHELIAL DYSFUNCTION; NO; POTENTIALS; CELLS; CGMP; ENOS;
D O I
10.1016/j.biopha.2018.07.044
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Ginsenoside Re (GS-Re) is one of the main ingredients of ginseng, a widely known Chinese traditional medicine, and has a variety of beneficial effects, including vasorelaxation, antioxidative, anti-inflammatory, and anticancer properties. The aims of the present study were to observe the effect of GS-Re on balloon injury-induced neointimal hyperplasia in the arteries and to investigate the mechanisms underlying this effect. A rat vascular neointimal hyperplasia model was generated by rubbing the endothelium of the common carotid artery (CCA) with a balloon, and GS-Re (12.5, 25 or 50 mg/kg/d) were subsequently continuously administered to the rats by gavage for 14 days. After GS-Re treatment, the vessel lumen of injured vessels showed significant increases in the GS-Re 25.0 and 50.0 mg/kg/d (intermediate- and high-dose) groups according to H.E. staining. Additionally, a reduced percentage of proliferating cell nuclear antigen (PCNA)-positive cells and an increased number of SM alpha-actin-positive cells were detected, and the levels of NO, cyclic guanosine monophosphate (cGMP), and eNOS mRNA as well as the phos-eNOS(ser1177)/eNOS protein ratio were obviously upregulated in the intermediate- and high-dose groups. Moreover, the promotive effects of GS-Re on NO and eNOS expression were blocked by L-NAME treatment to different degrees. These results suggested that GS-Re can suppress balloon injury-induced vascular neointimal hyperplasia by inhibiting VSMC proliferation, which is closely related to the activation of the eNOS/NO/cGMP pathway.
引用
收藏
页码:1091 / 1097
页数:7
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