• 1. Department of Cardiovascular Surgery, Third Hospital of Mianyang, Mianyang, 621000, Sichuan, P.R.China;
  • 2. Department of Cardiovascular Surgery, West China Hospital, Sichuan University, Chengdu, 610041, P.R.China;
HU Jia, Email: humanjia@msn.com
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Objective  To investigate the effect and mechanism of epigallocatechin-3-gallate (EGCG) on restenosis of the vein graft. Methods  Totally 90 Sprague-Dawley rats were randomly divided a the control group, a vein graft group and an EGCG+vein graft group. At week 1, 2 and 4, the intimal and tunica thickness of the venous graft wall was evaluated by hematoxylin-eosin staining, and the expression of Ki-67 was assessed by immunohistochemistry analysis, and then the expression of hairy and enhancer of split-1 (HES1) was measured by Western blot assay. Results  At week 2, the intimal thickness (46.76±4.89 μmvs. 8.93±0.82 μm, 46.76±4.89 μmvs. 34.24±3.57 μm), tunica thickness (47.28±4.37vs. 16.33±1.52 μm, 47.28±4.37vs. 36.27±3.29 μm), positive cell rate of Ki-67 (21.59%±2.29%vs. 1.12%±0.22%, 21.59%±2.29%vs. 15.38%±1.30%), expression of HES1 respectively increased in the experimental group than those in the control group and the EGCG+vein graft group (P<0.05, respectively). At week 4, the intimal thickness (66.38±6.23 μmvs. 8.29±0.79 μm, 66.38±6.23 μmvs. 48.39±4.23 μm), tunica thickness (63.27±6.18 μmvs. 15.29±1.49 μm, 63.27±6.18 μmvs. 44.63±4.49 μm), positive cell rate of Ki-67 (33.19%±3.03%vs. 1.09%±0.19%, 33.19%±3.03%vs. 24.37%±2.73%), expression of HES1 increased in the experimental group than those in the control group and EGCG+vein graft group (P<0.05, respectively). Conclusion  EGCG may inhibite restenosis of vein graft by inhibiting Notch signal pathway.

Citation: ZHANG Yi, GU Jun, LIU Linbo, LIAO Zhijie, ZHANG Hongwei, YANG Peng, FAN Kangjun, LIANG Huaimin, XIAO Zhenghua, HU Jia. Inhibitory effect and mechanism of epigallocatechin-3-gallate on autogenous vein graft stenosis in rat models. Chinese Journal of Clinical Thoracic and Cardiovascular Surgery, 2017, 24(10): 791-796. doi: 10.7507/1007-4848.201704044 Copy

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