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[基因型在抗精神病药物致僵效应中的作用]

[The role of the genotype in the cataleptogenic effect of neuroleptics].

作者信息

Skrinskaia Iu A, Nikulina E M, Popova N K

出版信息

Eksp Klin Farmakol. 1992 Nov-Dec;55(6):7-9.

PMID:1363957
Abstract

The cataleptogenic effects of three neuroleptics from one chemical group was investigated in 8 mice strains (CBA, A/He, C57B1/6, C3H/He, BALB/c, AKR, DD, and CC57Br. Despite significant interstrain, differences in the action of the drugs, haloperidol (0.5 mg/kg) and trifluperidol (0.5 mg/kg) produced much greater cataleptogenic action than fluspirilene (2 mg/kg). At the same time the intensity of catalepsy in various mice strains after haloperidol was not coincident with that after trifluperidol (r = 0.22): CBA mice displayed the maximum catalepsy, but AKR, DD and CC57Br mice, the minimum when haloperidol was given; with trifluperidol, the maximum catalepsy was observed in AKR mice, but absent in DD mice. Fluspirilene induced catalepsy only in CBA and A/He mice. Thus, the presence of catalepsy, a side effect of most neuroleptics, is largely predetermined by hereditary factors.

摘要

研究了来自同一化学组的三种抗精神病药物对8种小鼠品系(CBA、A/He、C57B1/6、C3H/He、BALB/c、AKR、DD和CC57Br)的致僵作用。尽管不同品系之间药物作用存在显著差异,但氟哌啶醇(0.5mg/kg)和三氟哌多(0.5mg/kg)产生的致僵作用比氟斯必灵(2mg/kg)大得多。同时,氟哌啶醇给药后不同小鼠品系的僵住强度与三氟哌多给药后的僵住强度不一致(r = 0.22):给予氟哌啶醇时,CBA小鼠僵住程度最大,而AKR、DD和CC57Br小鼠最小;给予三氟哌多时,AKR小鼠僵住程度最大,而DD小鼠无僵住现象。氟斯必灵仅在CBA和A/He小鼠中诱导出僵住。因此,僵住作为大多数抗精神病药物的一种副作用,在很大程度上由遗传因素决定。

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