Erratum to: ‘Serotonin uptake inhibitors modulate intracellular Ca2+ mobilization in platelets’ Eur. j. pharmacol. — Mol. pharmacol. sect. 288 (1995) 373–477

Daiga M. Helmeste , Siu W. Tang , Christopher Reist , Ryan Vu
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引用次数: 3

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.

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更正:“血清素摄取抑制剂调节血小板细胞内Ca2+动员”Eur。j .杂志。-摩尔,药物。第288节(1995)373-477
将血清素摄取抑制剂舍曲林、帕罗西汀和氟西汀与丙咪嗪、钙调素拮抗剂N-(6-氨基己基)-5-氯-1-萘磺酰胺(W-7)和卡咪唑进行比较,研究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素拮抗剂增强凝血酶介导的细胞内Ca2+升高。舍曲林、卡咪唑和W-7也引起细胞内Ca2+基线水平的大剂量依赖性增加。提高细胞内Ca2+的能力与抑制钙调素的能力之间存在粗略的相关性。新霉素是肌醇三磷酸(IP3)生成的抑制剂,能显著抑制舍他林的作用。这与IP3和钙调素在这些药物的作用中的作用是一致的。
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Author index Editorial Keyword index Ba2+ replaces Ca2+/calmodulin in the activation of protein phosphatases and in exocytosis of all major transmitters Potentiation and inhibition of subtypes of neuronal nicotinic acetylcholine receptors by Pb2+
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