Atwal K S
Bristol-Myers Squibb Pharmaceutical Research Institute, Princeton, New Jersey 08543-4000.
J Cardiovasc Pharmacol. 1994;24 Suppl 4:S12-7.
KATP openers are recognized as having a therapeutic potential for the treatment of various cardiovascular and noncardiovascular diseases. However, the first-generation agents open KATP in a variety of tissues that limit their potential clinical utility. This review describes our studies aimed at the identification of a common pharmacophore among structurally diverse KATP openers and the discovery of tissue-selective agents that may offer advantages over the first-generation agents for the treatment of cardiovascular diseases. Compounds (e.g., BMS-182264) combining the structural features of KATP openers cromakalim and pinacidil, show smooth-muscle relaxing and antihypertensive activities comparable to their predecessors, indicating cromakalim and pinacidil may express their biologic effects through similar structural requirements. The hypothesis about common features is further supported by radioligand-binding studies showing cromakalim, pinacidil, and the combination compound BMS-182264 bind to a similar receptor site in rat aortic smooth-muscle cells. Regardless of having a pharmacologic profile similar to cromakalim and pinacidil in vascular smooth muscle, BMS-182264 had no effect on action potential duration in guinea pig papillary muscle, indicating smooth-muscle selectivity for BMS-182264. We demonstrate that no correlation exists between anti-ischemic and smooth-muscle relaxing potencies for a variety of structurally different KATP openers. Efforts to find KATP openers selective for the ischemic myocardium led to the identification of BMS-180448 which, despite having similar anti-ischemic potency to cromakalim, was significantly less active as a smooth-muscle relaxant. This compound was shown to be efficacious as an anti-ischemic agent in vivo without affecting hemodynamic variables, a potential liability of first-generation compounds.(ABSTRACT TRUNCATED AT 250 WORDS)
钾离子通道开放剂被认为在治疗各种心血管疾病和非心血管疾病方面具有治疗潜力。然而,第一代药物在多种组织中开放钾离子通道,这限制了它们的潜在临床应用。本综述描述了我们旨在确定结构多样的钾离子通道开放剂之间的共同药效基团以及发现组织选择性药物的研究,这些组织选择性药物在治疗心血管疾病方面可能比第一代药物更具优势。结合钾离子通道开放剂克罗卡林和平尼地尔结构特征的化合物(如BMS - 182264),显示出与它们的前身相当的平滑肌舒张和降压活性,表明克罗卡林和平尼地尔可能通过相似的结构要求来发挥其生物学效应。放射性配体结合研究表明克罗卡林、平尼地尔和复合化合物BMS - 182264在大鼠主动脉平滑肌细胞中结合到相似的受体位点,这进一步支持了关于共同特征的假设。尽管BMS - 182264在血管平滑肌中的药理作用与克罗卡林和平尼地尔相似,但它对豚鼠乳头肌的动作电位持续时间没有影响,表明BMS - 182264具有平滑肌选择性。我们证明,对于各种结构不同的钾离子通道开放剂,抗缺血效力和平滑肌舒张效力之间不存在相关性。寻找对缺血心肌有选择性的钾离子通道开放剂的努力导致了BMS - 180448的发现,尽管它与克罗卡林具有相似的抗缺血效力,但作为平滑肌松弛剂的活性明显较低。该化合物在体内被证明是一种有效的抗缺血药物,而不影响血流动力学变量,这是第一代化合物的一个潜在问题。(摘要截断于250字)