氧化应激
高海拔对人类的影响
超氧化物歧化酶
丙二醛
高原病
缺氧(环境)
谷胱甘肽过氧化物酶
医学
内科学
抗氧化剂
内分泌学
化学
生物化学
氧气
解剖
有机化学
作者
Eduardo Pena,Samia El Alam,Patricia Siqués,Julio Brito
出处
期刊:Antioxidants
[Multidisciplinary Digital Publishing Institute]
日期:2022-01-28
卷期号:11 (2): 267-267
被引量:106
标识
DOI:10.3390/antiox11020267
摘要
Several diseases associated with high-altitude exposure affect unacclimated individuals. These diseases include acute mountain sickness (AMS), high-altitude cerebral edema (HACE), high-altitude pulmonary edema (HAPE), chronic mountain sickness (CMS), and, notably, high-altitude pulmonary hypertension (HAPH), which can eventually lead to right ventricle hypertrophy and heart failure. The development of these pathologies involves different molecules and molecular pathways that might be related to oxidative stress. Studies have shown that acute, intermittent, and chronic exposure to hypobaric hypoxia induce oxidative stress, causing alterations to molecular pathways and cellular components (lipids, proteins, and DNA). Therefore, the aim of this review is to discuss the oxidative molecules and pathways involved in the development of high-altitude diseases. In summary, all high-altitude pathologies are related to oxidative stress, as indicated by increases in the malondialdehyde (MDA) biomarker and decreases in superoxide dismutase (SOD) and glutathione peroxidase (GPx) antioxidant activity. In addition, in CMS, the levels of 8-iso-PGF2α and H2O2 are increased, and evidence strongly indicates an increase in Nox4 activity in HAPH. Therefore, antioxidant treatments seem to be a promising approach to mitigating high-altitude pathologies.
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