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波那普明及其代谢产物在离体大鼠心房中的抗胆碱能活性。

Anticholinergic activity of bornaprine and its metabolites in the isolated rat atrium.

作者信息

Hufford C D, Elmarakby S A, Walker L A

机构信息

Department of Pharmacognosy, University of Mississippi, University.

出版信息

Pharmacology. 1991;42(1):23-7. doi: 10.1159/000138764.

Abstract

These studies evaluated the antimuscarinic activity of bornaprine hydrochloride, a synthetic anticholinergic drug utilized in the treatment of parkinsonism. Several of its metabolites were also evaluated. Biological activity was assessed by the ability of the compounds to inhibit the negative inotropic response to carbachol in the isolated left atrium of the rat. Bornaprine showed a pA2 value (concentration required to reduce the agonist response by 50%) of 7.27 +/- 0.21. The exo and endo epimers were approximately equipotent in this regard. One metabolite, the 5-hydroxyl, showed similar activity to the parent compound, whereas 2 other hydroxylated metabolites showed much less effect.

摘要

这些研究评估了盐酸博那普明的抗毒蕈碱活性,盐酸博那普明是一种用于治疗帕金森病的合成抗胆碱能药物。还对其几种代谢物进行了评估。通过化合物抑制大鼠离体左心房对卡巴胆碱的负性肌力反应的能力来评估生物活性。博那普明的pA2值(使激动剂反应降低50%所需的浓度)为7.27±0.21。在这方面,外型和内型差向异构体的效力大致相当。一种代谢物,即5-羟基代谢物,显示出与母体化合物相似的活性,而其他两种羟基化代谢物的作用则小得多。

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