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存在一种新的血浆因子的证据,该因子与ADP诱导的血小板聚集起协同作用。

Evidence for the presence of a new plasma factor which acts synergistically to ADP induced platelet aggregation.

作者信息

Dikshit M, Srimal R C

机构信息

Division of Pharmacology, Central Drug Research Institute, Lucknow, India.

出版信息

Life Sci. 1990;47(2):117-26. doi: 10.1016/0024-3205(90)90224-f.

Abstract

The existence of a new factor (AF) in mice acting synergistically with known proaggregatory stimuli has been suggested by the present study in the plasma of mice challenged with intravenous collagen and adrenaline. Indomethacin, nordihydroguaretic acid (NDGA), BW 755C, phentolamine, cimetidine and ketanserin could not block the response of AF. Activity of the factor remained unaltered after treatment with pancreatic phospholipase A2, collagenase, CP/CPK, trypsin and heparin. Fractionation of the plasma indicated the presence of AF in acetone precipitate. Activity was destroyed by pronase and it was lost after dialysis and charcoal treatment. Existence of such a factor which is heat resistant, is of low molecular weight and is proaggregatory in nature in the thrombotic mice plasma and which requires calcium ions for the expression of its activity, has not been reported earlier.

摘要

本研究在静脉注射胶原蛋白和肾上腺素的小鼠血浆中发现,小鼠体内存在一种新因子(AF),它与已知的促聚集刺激物协同作用。吲哚美辛、去甲二氢愈创木酸(NDGA)、BW 755C、酚妥拉明、西咪替丁和酮色林均不能阻断AF的反应。用胰磷脂酶A2、胶原酶、CP/CPK、胰蛋白酶和肝素处理后,该因子的活性保持不变。血浆分级分离表明丙酮沉淀物中存在AF。该活性被链霉蛋白酶破坏,经透析和活性炭处理后丧失。血栓形成小鼠血浆中存在这样一种耐热、低分子量且本质上具有促聚集性且其活性表达需要钙离子的因子,此前尚未见报道。

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