Suppr超能文献

外周血血小板的药物易损性。

Drug vulnerability of peripheral blood platelets.

作者信息

Djaldetti M

出版信息

Arch Toxicol Suppl. 1983;6:21-32. doi: 10.1007/978-3-642-69083-9_3.

Abstract

The effect of antiinflammatory drugs (aspirin, Voltaren), cytotoxic drugs (cyclophosphamide, vincristine), antibiotics (penicillin, chloramphenicol), as well as of dipyridamole on the different ultrastructural and metabolic parameters of human platelets was examined in vitro. Almost all drugs caused a decreased platelet aggregation but of different degrees. The alteration of the internal structure consisted of a decrease in the number of platelet granules, displacement of the granules and mitochondrial damage. The surface alterations affected the number and appearance of platelet pseudopodia. With the exception of Voltaren the drugs exerted an inhibitory effect on platelet protein synthesizing capacity and on their phagocytotic ability. Voltaren stimulated the ability of platelets to engulf latex particles.

摘要

在体外研究了抗炎药(阿司匹林、扶他林)、细胞毒性药物(环磷酰胺、长春新碱)、抗生素(青霉素、氯霉素)以及双嘧达莫对人血小板不同超微结构和代谢参数的影响。几乎所有药物都导致血小板聚集减少,但程度不同。内部结构的改变包括血小板颗粒数量减少、颗粒移位和线粒体损伤。表面改变影响血小板伪足的数量和外观。除扶他林外,这些药物对血小板蛋白质合成能力及其吞噬能力均有抑制作用。扶他林刺激血小板吞噬乳胶颗粒的能力。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验