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钙调蛋白拮抗剂W-7可抑制血小板活化因子诱导的人血小板聚集。

Calmodulin antagonist W-7 inhibits aggregation of human platelets induced by platelet activating factor.

作者信息

Levy J V

出版信息

Proc Soc Exp Biol Med. 1983 Mar;172(3):393-5. doi: 10.3181/00379727-172-3-rc1.

Abstract

Experiments were done to test the hypothesis that aggregation of human platelets induced by platelet activating factor (PAF) may be mediated by calmodulin-dependent processes. W-7 [N-(6-aminohexyl)-5-chloro-1-naphthalene sulfonamide], a potent calmodulin antagonist, caused dose-dependent inhibition of PAF induced aggregation of human platelets in vitro. The ED50 for W-7 was 51.5 +/- 9.5 microM (mean +/- SEM). This concentration is known to be platelet calmodulin-specific. These data are consistent with the hypothesis.

摘要

开展实验以检验如下假说

血小板活化因子(PAF)诱导的人血小板聚集可能由钙调蛋白依赖性过程介导。W-7 [N-(6-氨基己基)-5-氯-1-萘磺酰胺],一种有效的钙调蛋白拮抗剂,在体外对PAF诱导的人血小板聚集产生剂量依赖性抑制。W-7的半数有效剂量(ED50)为51.5 +/- 9.5微摩尔(平均值 +/- 标准误)。已知该浓度具有血小板钙调蛋白特异性。这些数据与该假说相符。

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