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[诱发尾状核电位的药理学修饰]

[Pharmacological modification of evoked caudate nucleus potentials].

作者信息

Lehmann K, Andreas K

出版信息

Acta Biol Med Ger. 1979;38(9):1323-30.

PMID:550668
Abstract

To stimulation of the Substantia nigra the nucleus caudatoputamen of the rat responds with the release of a short-latent sum action potential that may serve to characterize the interaction between the two nuclear areas. The partly conflicting results reported in the literature about drug effects on this potential prompted us to examine the effectiveness of dopaminergic and cholinergic substances or their antagonists following systematic administration. Chloropromazine increases the amplitude of the potential, while apomorphine has a distinct antagonistic effect. Interesting appear to be the analogical effects of Tricuran, arecoline and apomorphine, and the furtherance of the chloropromazine effect by arecoline.

摘要

刺激大鼠的黑质时,尾状核壳核会以释放短潜伏期总和动作电位做出反应,这可能有助于表征这两个核区之间的相互作用。文献中报道的关于药物对该电位影响的部分相互矛盾的结果促使我们研究多巴胺能和胆碱能物质或其拮抗剂经系统给药后的效果。氯丙嗪会增加电位的幅度,而阿扑吗啡有明显的拮抗作用。曲古抑菌素、槟榔碱和阿扑吗啡的类似作用,以及槟榔碱对氯丙嗪作用的促进作用似乎很有趣。

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