Department of Pediatrics, NYU School of Medicine, New York, NY 10016, United States; Department of Physiology & Neuroscience, NYU School of Medicine, New York, NY 10016, United States; Department of Biochemistry and Molecular Pharmacology, NYU School of Medicine, New York, NY 10016, United States.
Pharmacol Ther. 2013 Nov;140(2):167-75. doi: 10.1016/j.pharmthera.2013.06.007. Epub 2013 Jun 19.
Diazoxide has been identified over the past 50years to have a number of physiological effects, including lowering the blood pressure and rectifying hypoglycemia. Today it is used clinically to treat these conditions. More recently, another important mode of action emerged: diazoxide has powerful protective properties against cardiac ischemia. The heart has intrinsic protective mechanisms against ischemia injury; one of which is ischemic preconditioning. Diazoxide mimics ischemic preconditioning. The purpose of this treatise is to review the literature in an attempt to identify the many effectors of diazoxide and discuss how they may contribute to diazoxide's cardioprotective properties. Particular emphasis is placed on the concentration ranges in which diazoxide affects its different targets and how this compares with the concentrations commonly used to study cardioprotection. It is concluded that diazoxide may have several potential effectors that may potentially contribute to cardioprotection, including KATP channels in the pancreas, smooth muscle, endothelium, neurons and the mitochondrial inner membrane. Diazoxide may also affect other ion channels and ATPases and may directly regulate mitochondrial energetics. It is possible that the success of diazoxide lies in this promiscuity and that the compound acts to rebalance multiple physiological processes during cardiac ischemia.
二氮嗪在过去 50 年中被发现具有多种生理作用,包括降低血压和纠正低血糖。如今,它在临床上被用于治疗这些疾病。最近,另一种重要的作用模式出现了:二氮嗪对心肌缺血具有强大的保护作用。心脏具有内在的保护机制来对抗缺血损伤;其中之一是缺血预处理。二氮嗪模拟缺血预处理。本文的目的是回顾文献,试图确定二氮嗪的许多效应物,并讨论它们如何有助于二氮嗪的心脏保护特性。特别强调了二氮嗪影响其不同靶标的浓度范围,以及这与常用于研究心脏保护的浓度的比较。结论是,二氮嗪可能有几个潜在的效应物,可能有助于心脏保护,包括胰腺、平滑肌、内皮细胞、神经元和线粒体内膜中的 KATP 通道。二氮嗪还可能影响其他离子通道和 ATP 酶,并可能直接调节线粒体能量代谢。二氮嗪的成功可能在于其这种混杂性,该化合物在心脏缺血期间作用于重新平衡多个生理过程。