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氧化应激对冠状动脉微循环的血管运动调节:精氨酸酶的作用。

Vasomotor regulation of coronary microcirculation by oxidative stress: role of arginase.

机构信息

Department of Medical Physiology, Scott & White Healthcare, Texas A&M Health Science Center , Temple, TX , USA ; Department of Surgery, College of Medicine, Scott & White Healthcare, Texas A&M Health Science Center , Temple, TX , USA.

出版信息

Front Immunol. 2013 Aug 19;4:237. doi: 10.3389/fimmu.2013.00237. eCollection 2013.

Abstract

Overproduction of reactive oxygen species, i.e., oxidative stress, is associated with the activation of redox signaling pathways linking to inflammatory insults and cardiovascular diseases by impairing endothelial function and consequently blood flow dysregulation due to microvascular dysfunction. This review focuses on the regulation of vasomotor function in the coronary microcirculation by endothelial nitric oxide (NO) during oxidative stress and inflammation related to the activation of L-arginine consuming enzyme arginase. Superoxide produced in the vascular wall compromises vasomotor function by not only scavenging endothelium-derived NO but also inhibiting prostacyclin synthesis due to formation of peroxynitrite. The upregulation of arginase contributes to the deficiency of endothelial NO and microvascular dysfunction in various vascular diseases by initiating or following oxidative stress and inflammation. Hydrogen peroxide, a diffusible and stable oxidizing agent, exerts vasodilator function and plays important roles in the physiological regulation of coronary blood flow. In occlusive coronary ischemia, the release of hydrogen peroxide from the microvasculature helps to restore vasomotor function of coronary collateral microvessels with exercise training. However, excessive production and prolonged exposure of microvessels to hydrogen peroxide impairs NO-mediated endothelial function by reducing L-arginine availability through hydroxyl radical-dependent upregulation of arginase. The redox signaling can be a double-edged sword in the microcirculation, which helps tissue survival in one way by improving vasomotor regulation and elicits oxidative stress and tissue injury in the other way by causing vascular dysfunction. The impact of vascular arginase on the development of vasomotor dysfunction associated with angiotensin II receptor activation, hypertension, ischemia-reperfusion, hypercholesterolemia, and inflammatory insults is discussed.

摘要

活性氧(ROS)的过度产生,即氧化应激,与氧化还原信号通路的激活有关,这些信号通路与炎症损伤和心血管疾病有关,通过损害内皮功能,进而导致血管舒张功能障碍和血流调节异常。本综述重点讨论了内皮一氧化氮(NO)在氧化应激和炎症相关的情况下,调节冠状动脉微循环的血管舒缩功能,这种情况与消耗 L-精氨酸的酶——精氨酸酶的激活有关。血管壁中产生的超氧阴离子不仅通过清除内皮源性 NO,还通过形成过氧亚硝酸盐抑制前列环素合成,从而损害血管舒缩功能。在各种血管疾病中,精氨酸酶的上调通过引发或紧随氧化应激和炎症导致内皮 NO 缺乏和微血管功能障碍。过氧化氢是一种可扩散和稳定的氧化剂,具有血管舒张功能,在冠状动脉血流的生理调节中发挥重要作用。在闭塞性冠状动脉缺血中,微脉管系统从微脉管系统释放的过氧化氢有助于通过运动训练恢复冠状侧支微血管的血管舒缩功能。然而,微脉管系统中过氧化氢的过度产生和长时间暴露会通过羟基自由基依赖性精氨酸酶上调减少 L-精氨酸的可用性,从而损害 NO 介导的内皮功能。氧化还原信号在微循环中可能是一把双刃剑,一方面通过改善血管舒缩调节有助于组织存活,另一方面通过引起血管功能障碍导致氧化应激和组织损伤。讨论了血管性精氨酸酶在血管舒缩功能障碍的发展中的作用,这种功能障碍与血管紧张素Ⅱ受体激活、高血压、缺血再灌注、高胆固醇血症和炎症损伤有关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/92cb/3746455/8faee4e8e203/fimmu-04-00237-g001.jpg

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