bopinddolol:药理基础和临床意义

T. Nagatomo, Y. Hosohata, T. Ohnuki, Takashi Nakamura, K. Hattori, J. Suzuki, M. Ishiguro
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引用次数: 5

摘要

Bopindolol是一种β 1-和β 2-肾上腺素受体(ARs)的非选择性拮抗剂,通过药理学、分子生物学技术和分子模型研究发现,Bopindolol具有一些独特的性质。Bopindolol能持续阻断β 1-和β 2- ar,具有内在的拟交感神经和膜稳定作用,抑制肾素分泌,并与5-HT受体相互作用。此外,我们最近的分子模型研究确定了bopindolol和β - ar亚型之间可能的相互作用位点。回顾的研究支持我们的发现,bopinddolol对β 1-和β 2- ar无选择性,对β 3-AR亚型具有低亲和力,并且具有可能有益于心血管疾病治疗的药理特性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Bopindolol: Pharmacological Basis and Clinical Implications
: Bopindolol, a non-selective antagonist of beta 1- and beta 2-adrenoceptors (ARs), has been found by pharmacological, molecular biological techniques and molecular modeling to have several unique properties. Bopindolol produces sustained blockade of beta 1- and beta 2-ARs, has intrinsic sympathomimetic as well as membrane stabilizing actions, inhibits renin secretion, and interacts with 5-HT receptors. Also, our recent molecular modeling studies identified possible interaction sites between bopindolol and beta-AR subtypes. The reviewed studies support our findings that bopindolol is non-selective for beta 1- and beta 2-ARs, has low affinity for beta 3-AR subtype and has pharmacological properties that are likely to be beneficial in the treatment of cardiovascular diseases.
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