Zhou Li, Chen Ping, Peng Yating, Ouyang Ruoyun
Department of Respiratory Medicine, The Second Xiangya Hospital, Central South University, 139 Renming Middle Road, Changsha, Hunan 410011, China; Research Unit of Respiratory Disease, Central South University, 139 Renming Middle Road, Changsha, Hunan 410011, China; Treatment Center of Respiratory Disease, Central South University, 139 Renming Middle Road, Changsha, Hunan 410011, China.
Oxid Med Cell Longev. 2016;2016:9626831. doi: 10.1155/2016/9626831. Epub 2016 Sep 28.
Obstructive sleep apnea syndrome (OSAS) is characterized by chronic nocturnal intermittent hypoxia and sleep fragmentations. Neurocognitive dysfunction, a significant and extraordinary complication of OSAS, influences patients' career, family, and social life and reduces quality of life to some extent. Previous researches revealed that repetitive hypoxia and reoxygenation caused mitochondria and endoplasmic reticulum dysfunction, overactivated NADPH oxidase, xanthine oxidase, and uncoupling nitric oxide synthase, induced an imbalance between prooxidants and antioxidants, and then got rise to a series of oxidative stress (OS) responses, such as protein oxidation, lipid peroxidation, and DNA oxidation along with inflammatory reaction. OS in brain could trigger neuron injury especially in the hippocampus and cerebral cortex regions. Those two regions are fairly susceptible to hypoxia and oxidative stress production which could consequently result in cognitive dysfunction. Apart from continuous positive airway pressure (CPAP), antioxidant may be a promising therapeutic method to improve partially reversible neurocognitive function. Understanding the role that OS played in the cognitive deficits is crucial for future research and therapeutic strategy development. In this paper, recent important literature concerning the relationship between oxidative stress and cognitive impairment in OSAS will be summarized and the results can provide a rewarding overview for future breakthrough in this field.
阻塞性睡眠呼吸暂停综合征(OSAS)的特征是慢性夜间间歇性缺氧和睡眠片段化。神经认知功能障碍是OSAS一种显著且特殊的并发症,会影响患者的职业、家庭和社交生活,并在一定程度上降低生活质量。先前的研究表明,反复缺氧和复氧会导致线粒体和内质网功能障碍,过度激活烟酰胺腺嘌呤二核苷酸磷酸(NADPH)氧化酶、黄嘌呤氧化酶和解偶联型一氧化氮合酶,引发促氧化剂和抗氧化剂之间的失衡,进而引发一系列氧化应激(OS)反应,如蛋白质氧化、脂质过氧化和DNA氧化以及炎症反应。大脑中的OS会引发神经元损伤,尤其是在海马体和大脑皮质区域。这两个区域对缺氧和氧化应激的产生相当敏感,进而可能导致认知功能障碍。除持续气道正压通气(CPAP)外,抗氧化剂可能是一种有前景的治疗方法,可部分改善可逆性神经认知功能。了解OS在认知缺陷中所起的作用对于未来的研究和治疗策略的制定至关重要。本文将总结近期有关OSAS中氧化应激与认知障碍关系的重要文献,其结果可为该领域未来的突破提供有益的概述。