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抗抑郁药和抗精神病药对人血小板中5HT2受体介导的信号转导系统的影响。

Effects of Antidepressants and antipsychotics on the 5HT2 receptor-mediated signal transducing system in human platelets.

作者信息

Ohsuka N, Mashiko H, Kaneko M, Kumashiro H

机构信息

Department of Neuropsychiatry, Fukushima Medical College, Japan.

出版信息

Psychopharmacology (Berl). 1995 Oct;121(4):428-32. doi: 10.1007/BF02246490.

Abstract

The IC50 values of the antidepressants amoxapine, mianserin, desipramine, clomipramine and imipramine, and the antipsychotics spiroperidol, chlorpromazine, levomepromazine and haloperidol for 3H-ketanserin binding, 5HT-induced intracellular Ca2+ increase, 5HT-induced shape change and 3H-paroxetine binding in human platelets were measured and the correlations of each parameter were examined. Results were as follows. Both the antidepressants and the antipsychotics had inhibitory effects on 3H-ketanserin binding, 5HT-induced intracellular Ca2+ increase and 5HT-induced shape change and there were significant positive correlations between the IC50 values of these three parameters. On the other hand, there were no significant correlations between the IC50 values in 3H-paroxetine binding and those in the other three parameters. These results suggest that 3H-ketanserin binding, 5HT-induced intracellular Ca2+ increase and 5HT-induced shape change are useful and reliable tools for the assessment of the effects of the antidepressants and the antipsychotics on the 5HT2 receptor-mediated signal transducing system in human platelets.

摘要

测定了抗抑郁药阿莫沙平、米安色林、地昔帕明、氯米帕明和丙咪嗪,以及抗精神病药螺哌啶醇、氯丙嗪、左美丙嗪和氟哌啶醇对人血小板中3H-酮色林结合、5-羟色胺(5HT)诱导的细胞内钙离子(Ca2+)增加、5HT诱导的形态变化和3H-帕罗西汀结合的半数抑制浓度(IC50)值,并检测了各参数之间的相关性。结果如下。抗抑郁药和抗精神病药均对3H-酮色林结合、5HT诱导的细胞内Ca2+增加和5HT诱导的形态变化有抑制作用,且这三个参数的IC50值之间存在显著正相关。另一方面,3H-帕罗西汀结合的IC50值与其他三个参数的IC50值之间无显著相关性。这些结果表明,3H-酮色林结合、5HT诱导的细胞内Ca2+增加和5HT诱导的形态变化是评估抗抑郁药和抗精神病药对人血小板中5HT2受体介导的信号转导系统作用的有用且可靠的工具。

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