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血清素摄取抑制剂可调节血小板内的钙离子动员。

Serotonin uptake inhibitors modulate intracellular Ca2+ mobilization in platelets.

作者信息

Helmeste D M, Tang S W, Reist C, Vu R

机构信息

Department of Psychiatry, Veterans Administration Medical Center, Long Beach, CA 90822, USA.

出版信息

Eur J Pharmacol. 1995 Feb 15;288(3):373-7. doi: 10.1016/0922-4106(95)90051-9.

Abstract

The serotonin uptake inhibitors sertraline, paroxetine and fluoxetine were compared with imipramine and the calmodulin antagonists N-(6-aminohexyl)-5-chloro-1-naphthalene-sulfonamide (W-7) and calmidazolium, for their effects on intracellular Ca2+ mobilization in human platelets. All serotonin uptake inhibitors and calmodulin antagonists augmented thrombin-mediated increases in intracellular Ca2+. Sertraline, calmidazolium and W-7 also caused large dose-dependent increases in baseline levels of intracellular Ca2+. There was a rough correlation between the ability to elevate intracellular Ca2+ and potencies for inhibition of calmodulin. Neomycin, an inhibitor of inositol trisphosphate (IP3) generation, significantly inhibited the effects of sertaline. This is consistent with a role of IP3 and calmodulin in the effects of these drugs.

摘要

将血清素摄取抑制剂舍曲林、帕罗西汀和氟西汀与丙咪嗪以及钙调蛋白拮抗剂N-(6-氨基己基)-5-氯-1-萘磺酰胺(W-7)和氯米达唑进行比较,观察它们对人血小板细胞内Ca2+动员的影响。所有血清素摄取抑制剂和钙调蛋白拮抗剂均增强了凝血酶介导的细胞内Ca2+增加。舍曲林、氯米达唑和W-7还导致细胞内Ca2+基线水平出现大剂量依赖性增加。提高细胞内Ca2+的能力与抑制钙调蛋白的效力之间存在大致的相关性。肌醇三磷酸(IP3)生成抑制剂新霉素显著抑制了舍曲林的作用。这与IP3和钙调蛋白在这些药物作用中的作用一致。

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