Liu Victor W T, Huang Paul L
Cardiovascular Research Center, Massachusetts General Hospital and Harvard Medical School, Boston, MA 02114, United States.
Cardiovasc Res. 2008 Jan;77(1):19-29. doi: 10.1016/j.cardiores.2007.06.024.
Nitric oxide (NO) is a gaseous molecule that plays many key roles in the cardiovascular system. Each of the enzymes that generate NO--neuronal, inducible and endothelial NO synthase-has been genetically disrupted in mice. This review discusses the cardiovascular phenotypes of each of the NO synthase (NOS) gene knockout mice, and the insights gained into the roles of NO in the cardiovascular system. Mice lacking the endothelial isoform are hypertensive, have endothelial dysfunction and show a more severe outcome in response to vascular injury, to stroke and cerebral ischaemia, and to diet-induced atherosclerosis. Mice lacking the neuronal isoform show a less severe outcome in response to stroke and cerebral ischaemia but have increased diet-induced atherosclerosis. Mice lacking the inducible isoform show reduced hypotension to septic shock. Together, NOS gene knockout mice have been useful tools that complement our other approaches to studying the multiple roles of NO in the cardiovascular system.
一氧化氮(NO)是一种气态分子,在心血管系统中发挥着许多关键作用。产生NO的每种酶——神经元型、诱导型和内皮型一氧化氮合酶——在小鼠中都已被基因敲除。本综述讨论了每种一氧化氮合酶(NOS)基因敲除小鼠的心血管表型,以及在了解NO在心血管系统中的作用方面所获得的见解。缺乏内皮型异构体的小鼠患有高血压,存在内皮功能障碍,并且在应对血管损伤、中风和脑缺血以及饮食诱导的动脉粥样硬化时表现出更严重的后果。缺乏神经元型异构体的小鼠在应对中风和脑缺血时表现出不太严重的后果,但饮食诱导的动脉粥样硬化有所增加。缺乏诱导型异构体的小鼠对感染性休克的低血压反应减弱。总之,NOS基因敲除小鼠是有用的工具,补充了我们研究NO在心血管系统中多种作用的其他方法。