Daiga M. Helmeste , Siu W. Tang , Christopher Reist , Ryan Vu
{"title":"Erratum to: ‘Serotonin uptake inhibitors modulate intracellular Ca2+ mobilization in platelets’ Eur. j. pharmacol. — Mol. pharmacol. sect. 288 (1995) 373–477","authors":"Daiga M. Helmeste , Siu W. Tang , Christopher Reist , Ryan Vu","doi":"10.1016/0922-4106(95)90034-9","DOIUrl":null,"url":null,"abstract":"<div><p>The serotonin uptake inhibitors sertraline, paroxetine and fluoxetine were compared with imipramine and the calmodulin antagonists <em>N</em>-(6-aminohexyl)-5-chloro-1-naphthalene-sulfonamide (W-7) and calmidazolium, for their effects on intracellular Ca<sup>2+</sup> mobilization in human platelets. All serotonin uptake inhibitors and calmodulin antagonists augmented thrombin-mediated increases in intracellular Ca<sup>2+</sup>. Sertraline, calmidazolium and W-7 also caused large dose-dependent increases in baseline levels of intracellular Ca<sup>2+</sup>. There was a rough correlation between the ability to elevate intracellular Ca<sup>2+</sup> and potencies for inhibition of calmodulin. Neomycin, an inhibitor of inositol trisphosphate (IP<sub>3</sub>) generation, significantly inhibited the effects of sertaline. This is consistent with a role of IP<sub>3</sub> and calmodulin in the effects of these drugs.</p></div>","PeriodicalId":100502,"journal":{"name":"European Journal of Pharmacology: Molecular Pharmacology","volume":"290 2","pages":"Pages 173-174"},"PeriodicalIF":0.0000,"publicationDate":"1995-07-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0922-4106(95)90034-9","citationCount":"3","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"European Journal of Pharmacology: Molecular Pharmacology","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/0922410695900349","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
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.