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微循环中血小板聚集与血流流变学相关的病理生理学方面。

Pathophysiological aspects of platelet aggregation in relation to blood flow rheology in microcirculation.

作者信息

Neri Serneri G G

出版信息

Ric Clin Lab. 1981;11 Suppl 1:39-46.

PMID:6765141
Abstract

Platelet aggregates play an important role in rheology of the blood flow in microcirculation. The formation of platelet aggregates markedly raise the threshold diameter of the vessel at which the inversion of Fahraeus-Lindquist effect takes place. In different diseases (ischemic heart disease, diabetes) thromboxane A2 production by platelets is increased and, as a consequence, platelet aggregate formation is facilitated. Platelet aggregation is modulated by several mechanisms, among which thromboxane A2 and thrombin increase and prostacyclin decrease formation of platelet aggregates. Prostacyclin is able also to increase blood red cells deformability thus it appears one of the most important factors for the control of blood flow rheology in microcirculation. However, prostacyclin production is limited in time, and repeated and close periods of venous stasis induce exhaustion of prostacyclin production and increase the formation of platelet aggregates.

摘要

血小板聚集体在微循环血流变学中起重要作用。血小板聚集体的形成显著提高了发生法赫瑞厄斯-林德奎斯特效应反转时的血管临界直径。在不同疾病(缺血性心脏病、糖尿病)中,血小板生成血栓素A2增加,结果促进了血小板聚集体的形成。血小板聚集受多种机制调节,其中血栓素A2和凝血酶增加而前列环素减少血小板聚集体的形成。前列环素还能够增加血液红细胞的变形能力,因此它似乎是控制微循环血流变学的最重要因素之一。然而,前列环素的生成在时间上是有限的,反复且紧密的静脉淤滞期会导致前列环素生成耗竭并增加血小板聚集体的形成。

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