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多巴胺能对肾上腺素能神经传递的抑制作用作为多巴胺受体机制研究的模型。

Dopaminergic inhibition of adrenergic neurotransmission as a model for studies on dopamine receptor mechanisms.

作者信息

Steinsland O S, Hieble J P

出版信息

Science. 1978 Jan 27;199(4327):443-5. doi: 10.1126/science.22933.

Abstract

Dopamine and apomorphine produced concentration-dependent inhibition of adrenergic neurotransmission in the isolated, perfused, rabbit ear artery. The inhibitory action of both dopamine and apomorphine was competitively antagonized by haloperidol and several other antipsychotic drugs. The calculated affinities of these drugs for the dopaminergic receptor correlate closely with both the pharmacological potencies of these drugs in vivo and their reported potencies as inhibitors of [3H]haloperidol binding to "dopamine receptors" in brain homogenates.

摘要

多巴胺和阿扑吗啡对离体灌注兔耳动脉的肾上腺素能神经传递产生浓度依赖性抑制作用。多巴胺和阿扑吗啡的抑制作用均被氟哌啶醇和其他几种抗精神病药物竞争性拮抗。计算得出这些药物对多巴胺能受体的亲和力与它们在体内的药理效力以及它们作为[3H]氟哌啶醇与脑匀浆中“多巴胺受体”结合抑制剂的报道效力密切相关。

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