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[乙莫辛和乙噻嗪对脑纹状体系统多巴胺能腺苷酸环化酶的作用]

[Action of etmozin and ethacizin on dopaminergic adenylate cyclase of the striate system of the brain].

作者信息

Baldenkov G N, Ratner E I, Rozenshtraukh L V, Tkachuk V A

出版信息

Biull Eksp Biol Med. 1984 Oct;98(10):448-50.

PMID:6149776
Abstract

The authors studied the effect of phenothiazine and butyrophenone neuroleptics and that of the antiarrhythmic drugs etmozine and etacizine on the dopamine--activated adenylate cyclase of the rabbit brain striatum. It was shown that all the neuroleptics under study prevented the development of the activating effect of dopamine, whereas the antiarrhythmic drugs administered at the same concentrations did not influence adenylate cyclase stimulation with dopamine. The affinity of etmozine and etacizine for dopamine receptors was 15-20 times less than the affinity of the typical neuroleptic trifluoroperazine. It is concluded that application of etmozine and etacizine to the treatment of arrhythmias is not complicated by neuroleptic or other dopaminergic effects of these drugs.

摘要

作者研究了吩噻嗪类和丁酰苯类抗精神病药物以及抗心律失常药物乙吗噻嗪和乙氧噻嗪对兔脑纹状体中多巴胺激活的腺苷酸环化酶的影响。结果表明,所有研究的抗精神病药物均能阻止多巴胺激活作用的发展,而相同浓度下给予的抗心律失常药物对多巴胺刺激腺苷酸环化酶没有影响。乙吗噻嗪和乙氧噻嗪对多巴胺受体的亲和力比对典型抗精神病药物三氟拉嗪的亲和力低15 - 20倍。结论是,使用乙吗噻嗪和乙氧噻嗪治疗心律失常不会因这些药物的抗精神病或其他多巴胺能效应而变得复杂。

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