首页> 外文期刊>Journal of the American College of Cardiology >Time courses of apoptosis and cell proliferation and their relationship to arterial remodeling and restenosis after angioplasty in an atherosclerotic rabbit model.
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Time courses of apoptosis and cell proliferation and their relationship to arterial remodeling and restenosis after angioplasty in an atherosclerotic rabbit model.

机译:动脉粥样硬化兔模型中血管成形术后细胞凋亡和细胞增殖的时程及其与动脉重塑和再狭窄的关系。

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OBJECTIVES: We sought to evaluate whether cellular mass changes (including apoptosis and proliferation) after arterial injury could interact with restenosis and arterial remodeling. BACKGROUND: The mechanisms controlling arterial remodeling after angioplasty remain poorly understood. Apoptosis and cell proliferation have been previously described after balloon angioplasty. However, their importance in the occurrence of arterial remodeling and restenosis is unknown. METHODS: Atherosclerosis was induced in 48 femoral arteries of New Zealand White rabbits by air-desiccation and a high-cholesterol diet. One month later, angioplasty was performed in 40 arteries. Apoptosis, cell proliferation, residual stenosis and arterial remodeling were evaluated at 2 h and 3, 7, 14, 21 and 28 days after angioplasty. RESULTS: Cell proliferation and apoptosis profiles were similar, but the peak in cell proliferation occurred approximately four days earlier than the peak in apoptosis in the neointima and media. Apoptosis density was positively correlated with arterial remodeling in the neointima and media (r = 0.69, p = 0.005 and r = 0.50, p = 0.05, respectively). Moreover, residual stenosis was inversely correlated with apoptosis density in the neointima and media (r = -0.62, p = 0.008 and r = -0.52, p = 0.04, respectively). In contrast, cell proliferation was independent of restenosis and arterial remodeling. CONCLUSIONS: In this model, cell proliferation preceded apoptosis throughout the four weeks after angioplasty. Apoptosis was inversely correlated with restenosis. Interestingly, apoptosis was also related to enlargement remodeling after balloon angioplasty.
机译:目的:我们试图评估动脉损伤后细胞质量的变化(包括凋亡和增殖)是否可能与再狭窄和动脉重构相互作用。背景:血管成形术后控制动脉重塑的机制仍知之甚少。先前已经描述了球囊血管成形术后的凋亡和细胞增殖。但是,它们在动脉重塑和再狭窄发生中的重要性尚不清楚。方法:通过空气干燥和高胆固醇饮食在新西兰白兔的48条股动脉中诱发动脉粥样硬化。一个月后,在40条动脉中进行了血管成形术。在血管成形术后2小时和3、7、14、21和28天评估细胞凋亡,细胞增殖,残余狭窄和动脉重塑。结果:细胞增殖和凋亡特征相似,但是细胞增殖的峰值比新内膜和培养基中的凋亡峰值提前约四天。细胞凋亡密度与新内膜和中膜的动脉重构呈正相关(r = 0.69,p = 0.005和r = 0.50,p = 0.05)。此外,残余狭窄与新内膜和中膜的细胞凋亡密度呈负相关(r = -0.62,p = 0.008和r = -0.52,p = 0.04)。相反,细胞增殖与再狭窄和动脉重构无关。结论:在该模型中,在血管成形术后的四个星期内,细胞增殖先于凋亡。细胞凋亡与再狭窄呈负相关。有趣的是,凋亡也与球囊血管成形术后的肿大重塑有关。

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