SEROTONIN UPTAKE INHIBITORS MODULATE INTRACELLULAR CA2+ MOBILIZATION IN PLATELETS

被引:49
作者
HELMESTE, DM [1 ]
TANG, SW [1 ]
REIST, C [1 ]
VU, R [1 ]
机构
[1] VET ADM MED CTR,DEPT PSYCHIAT,LONG BEACH,CA 90822
来源
EUROPEAN JOURNAL OF PHARMACOLOGY-MOLECULAR PHARMACOLOGY SECTION | 1995年 / 288卷 / 03期
关键词
5-HT; (5-HYDROXYTRYPTAMINE; SEROTONIN) UPTAKE INHIBITOR; CALMODULIN; CA2+; PLATELET; THROMBIN;
D O I
10.1016/0922-4106(95)90051-9
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
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.
引用
收藏
页码:373 / 377
页数:5
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