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Analysis of Trigger Mechanisms for Inflammation in Cardiovascular Disease: Application to Shock and Multiorgan Failure

机译:心血管疾病炎症的触发机制分析:休克和多功能失败的应用

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Cell activation in the microcirculation and inflammatory mediators have become a central focus of research into many cardiovascular diseases. However, the possible trigger mechanisms of inflammation remain less well understood. We summarize here a series of studies designed to investigate the origin of inflammation in acute physiological shock, a potentially lethal condition. A series of basic studies demonstrated that a major source of the inflammatory mediators in shock, produced in an ischemic intestine or after endotoxin administration, is due to the action of digestive enzymes. Many of these enzymes are proteases derived from the pancreas. The proteolytic and lipolytic action of pancreatic enzymes leads to the release of inflammatory mediators from the wall of the intestine. These mediators are transported via the intestinal microcirculation and the lymphatics into the central circulation, where they can initiate an inflammatory cascade with eventual multi-organ failure. These observations offer an opportunity for testing novel interventions against the lethal outcome of shock.
机译:微循环和炎症介质中的细胞活化已成为研究许多心血管疾病的中心重点。然而,炎症可能的触发机制仍然不太清楚。我们总结了这里的一系列研究,旨在探讨急性生理休克中炎症的起源,潜在的致命条件。一系列基本研究表明,在缺血性肠道或内毒素给药后产生的炎症介质的主要来源是由于消化酶的作用。许多这些酶是源自胰腺的蛋白酶。胰酶的蛋白水解和脂肪分解作用导致来自肠壁的炎症介质的释放。这些介质通过肠道微循环和淋巴管输送到中央循环中,在那里它们可以引发具有最终多器官衰竭的炎症级联。这些观察员提供了对休克致命结果进行测试的机会。

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