Literature DB >> 15372300

Local delivery of green tea catechins inhibits neointimal formation in the rat carotid artery injury model.

Dong-Woon Kim1, Young-Sun Park, Young-Gyu Kim, Hainan Piao, Jin-Sook Kwon, Kyung-Kuk Hwang, Tae-Jin Youn, Jong Bum Park, Yeo-Pyo Yun, Agapios Sachinidis, Chan-Hyung Kim, Myeong-Chan Cho, Hee-Yul Ahn.   

Abstract

It has been shown that green tea catechins (GTC) suppress proliferation of vascular smooth muscle cells (VSMCs) and that epigallocatechin-3-gallate (EGCG), which is a major constituent of GTC, selectively inhibits the platelet-derived growth factor-BB (PDGF-BB)-induced intracellular signaling transduction pathway. Vascular smooth muscle cell proliferation is one of major mechanisms of restenosis following percutaneous coronary intervention. This study tested whether GTC can inhibit VSMC proliferation and prevent neointimal formation in a rat carotid artery injury model. Vascular smooth muscle cell proliferation inhibition was analyzed with [3H]thymidine incorporation. Green tea catechins were applied to the endothelium-denuded carotid arteries of rats for 20 min. Angiography and morphometric analysis was performed after 2 weeks. Green tea catechins decreased [3H]thymidine incorporation stimulated with PDGF-BB dose dependently. In the absence of PDGF-BB, the decrement of [3H]thymidine incorporation was evident above a concentration of 10 micro g/ml of GTC. Carotid arteriographic evaluation showed that the minimum luminal diameter in the GTC-treated group (n=12) was 5.9 +/- 1.6 arbitrary units (a.u.) and was significantly larger than in the control group (4.3 +/- 1.4 a.u., n=10) ( P <0.05). The GTC-treated group also showed a significant reduction in neointimal formation compared with the control group (0.29 +/- 0.11 vs 0.42 +/- 0.10 mm2, P < 0.05). To identify the active ingredients, we performed a similar experiment using EGCG. The effects of EGCG were similar to those of GTC. Green tea catechins effectively inhibited VSMC proliferation. Neointimal formation was prevented in the rat carotid artery injury model by local delivery of GTC. As EGCG showed similar effects, it may be one of the major constituents of GTC having these effects.

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Year:  2004        PMID: 15372300     DOI: 10.1007/s00380-004-0768-6

Source DB:  PubMed          Journal:  Heart Vessels        ISSN: 0910-8327            Impact factor:   2.037


  4 in total

1.  Epigallocatechin-3-gallate is a potent phytochemical inhibitor of intimal hyperplasia in the wire-injured carotid artery.

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Journal:  J Vasc Surg       Date:  2013-03-26       Impact factor: 4.268

2.  Effects of simvastatin on cardiohemodynamic responses to ischemia-reperfusion in isolated rat hearts.

Authors:  Xia Zheng; Shen-Jiang Hu
Journal:  Heart Vessels       Date:  2006-03       Impact factor: 2.037

3.  Mitogenesis of vascular smooth muscle cell stimulated by platelet-derived growth factor-bb is inhibited by blocking of intracellular signaling by epigallocatechin-3-O-gallate.

Authors:  Mi Hee Lee; Byeong-Ju Kwon; Min-Ah Koo; Kyung Eun You; Jong-Chul Park
Journal:  Oxid Med Cell Longev       Date:  2013-11-06       Impact factor: 6.543

4.  Recent advances to accelerate re-endothelialization for vascular stents.

Authors:  Tarek M Bedair; Mahmoud A ElNaggar; Yoon Ki Joung; Dong Keun Han
Journal:  J Tissue Eng       Date:  2017-09-28       Impact factor: 7.813

  4 in total

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