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吡贝地尔的视网膜多巴胺能受体亲和力及眼部药代动力学特征

Retinal dopaminergic receptor affinity and ocular pharmacokinetic profile of piribedil.

作者信息

Lapalus P, Denis P, Drici M, Fredj-Reygrobellet D, Elena P P

机构信息

Department of Experimental and Clinical Pharmacology, Faculté de Médecine, Nice, France.

出版信息

J Neurol. 1992;239 Suppl 1:S17-21. doi: 10.1007/BF00819562.

Abstract

Binding studies on retinal dopamine receptors have revealed the existence of both D1 and D2 receptors. Human retina micro-autoradiographs confirm the distribution of dopaminergic receptors in the plexiform layers. Piribedil, a dopaminergic agonist, is able to bind to D2 receptors, while its metabolite (S584) preferentially displaces D1-specific radioligands. These results demonstrate that piribedil has a dopamine-like pharmacological profile including direct interaction with receptors. When instilled into the rabbit eye, piribedil penetrates rapidly and accumulates in the pigmented epithelia--the iris ciliary body and chorioretina--before being rapidly cleared. Macro-autoradiographs confirm this distribution and show the levels to be compatible with the affinity of piribedil for retinal dopaminergic receptors.

摘要

对视网膜多巴胺受体的结合研究揭示了D1和D2受体的存在。人类视网膜显微放射自显影片证实了多巴胺能受体在神经丛层中的分布。多巴胺能激动剂匹莫齐特能够与D2受体结合,而其代谢产物(S584)则优先置换D1特异性放射性配体。这些结果表明,匹莫齐特具有类似多巴胺的药理学特征,包括与受体的直接相互作用。当滴入兔眼时,匹莫齐特迅速渗透并积聚在色素上皮——虹膜睫状体和脉络膜视网膜——中,然后迅速清除。宏观放射自显影片证实了这种分布,并显示其水平与匹莫齐特对视网膜多巴胺能受体的亲和力相符。

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