Wessex Cardiothoracic Centre, BUPA Hospital, Southampton, UK.
Oxid Med Cell Longev. 2009 Nov-Dec;2(5):259-69. doi: 10.4161/oxim.2.5.9441.
During physiological processes molecules undergo chemical changes involving reducing and oxidizing reactions. A molecule with an unpaired electron can combine with a molecule capable of donating an electron. The donation of an electron is termed as oxidation whereas the gaining of an electron is called reduction. Reduction and oxidation can render the reduced molecule unstable and make it free to react with other molecules to cause damage to cellular and sub-cellular components such as membranes, proteins and DNA. In this paper, we have discussed the formation of reactive oxidant species originating from a variety of sources such as nitric oxide (NO) synthase (NOS), xanthine oxidases (XO), the cyclooxygenases, nicotinamide adenine dinucleotide phosphate (NAD(P)H) oxidase isoforms and metal-catalysed reactions. In addition, we present a treatise on the physiological defences such as specialized enzymes and antioxidants that maintain reduction-oxidation (redox) balance. We have also given an account of how enzymes and antioxidants can be exhausted by the excessive production of reactive oxidant species (ROS) resulting in oxidative stress/nitrosative stress, a process that is an important mediator of cell damage. Important aspects of redox imbalance that triggers the activity of a number of signalling pathways including transcription factors activity, a process that is ubiquitous in cardiovascular disease related to ischemia/reperfusion injury have also been presented.
在生理过程中,分子会经历涉及还原和氧化反应的化学变化。具有未配对电子的分子可以与能够提供电子的分子结合。电子的供体称为氧化,而电子的获得称为还原。还原和氧化可以使还原分子不稳定,并使其自由与其他分子反应,从而对细胞和亚细胞成分(如膜、蛋白质和 DNA)造成损伤。在本文中,我们讨论了源自多种来源的活性氧化剂的形成,例如一氧化氮(NO)合酶(NOS)、黄嘌呤氧化酶(XO)、环氧化酶、烟酰胺腺嘌呤二核苷酸磷酸(NAD(P)H)氧化酶同工型和金属催化反应。此外,我们还介绍了维持氧化还原(redox)平衡的生理防御机制,如专门的酶和抗氧化剂。我们还说明了在活性氧(ROS)过度产生的情况下,酶和抗氧化剂如何被耗尽,从而导致氧化应激/硝化应激,这是细胞损伤的重要介导过程。还介绍了引发许多信号通路(包括转录因子活性)活性的氧化还原失衡的重要方面,这一过程在与缺血/再灌注损伤相关的心血管疾病中普遍存在。