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生物人工心脏瓣膜的体外钙化:一种新方法的报告及相关生化因素综述

In vitro calcification of bioprosthetic heart valves: report of a novel method and review of the biochemical factors involved.

作者信息

Bernacca G M, Mackay T G, Wheatley D J

机构信息

University Department of Cardiac Surgery, Royal Infirmary, Glasgow.

出版信息

J Heart Valve Dis. 1992 Sep;1(1):115-30.

PMID:1341215
Abstract

The lifetime of bioprosthetic heart valves is limited by primary tissue failure and calcification of the valve leaflets. There are indications that synthetic elastomeric materials may also be subject to this problem. The mechanism of calcification is not known, but it is of interest that calcification can be induced in tissue even in the absence of cellular mechanisms, outside the body. Many hypotheses relate to inhibitory or promotory factors rather than primary instigators of calcification and none has led to a satisfactory solution of the problem. The study of calcification in replacement valves generally utilises in vivo test methods i.e. complex biologic systems. This creates difficulty in defining the primary factors involved. The use of in vitro test methods, including a novel fatigue tester method, has been reviewed. Various test media have been used, including simple salt solutions (allowing definition and controlled modification of the calcification medium) and bovine plasma. Comparison of static and dynamic in vitro methods with the rat subcutaneous implant model indicated a lower degree of calcification in vitro: the calcification achieved was, however, significantly greater than similar material not subject to calcification processes. Dynamic in vitro tests produced greater calcification than static in vitro tests. Porcine aortic valve material, in static tests, behaved similarly to bovine pericardium. In vitro calcification testing has a useful role to play in the economic screening of new materials or modifications of existing materials prior to in vivo testing. It may also aid the definition of the mechanism of calcification and hence the development of solutions to the problem.

摘要

生物人工心脏瓣膜的使用寿命受限于原发性组织衰竭和瓣膜小叶的钙化。有迹象表明,合成弹性体材料也可能存在这个问题。钙化的机制尚不清楚,但有趣的是,即使在体外没有细胞机制的情况下,钙化也能在组织中诱导产生。许多假说涉及钙化的抑制或促进因素,而非钙化的主要诱因,且没有一个假说能令人满意地解决这个问题。对置换瓣膜钙化的研究通常采用体内测试方法,即复杂的生物系统。这给确定其中的主要因素带来了困难。本文综述了包括一种新型疲劳测试仪方法在内的体外测试方法的应用。已使用了各种测试介质,包括简单盐溶液(可对钙化介质进行定义和可控修改)和牛血浆。将体外静态和动态方法与大鼠皮下植入模型进行比较表明,体外钙化程度较低:然而,所实现的钙化明显大于未经历钙化过程的类似材料。动态体外测试产生的钙化比静态体外测试更多。在静态测试中,猪主动脉瓣材料的表现与牛心包相似。体外钙化测试在体内测试之前对新材料或现有材料的改进进行经济筛选方面具有有用的作用。它还可能有助于确定钙化的机制,从而找到解决该问题的方法。

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