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环境性低氧状态下的骨骼肌能量代谢:迈向共识

Skeletal muscle energy metabolism in environmental hypoxia: climbing towards consensus.

作者信息

Horscroft James A, Murray Andrew J

机构信息

Department of Physiology, Development and Neuroscience, University of Cambridge, Downing Street, CB2 3EG Cambridge, UK.

出版信息

Extrem Physiol Med. 2014 Nov 28;3(1):19. doi: 10.1186/2046-7648-3-19. eCollection 2014.

Abstract

Skeletal muscle undergoes metabolic remodelling in response to environmental hypoxia, yet aspects of this process remain controversial. Broadly, environmental hypoxia has been suggested to induce: (i) a loss of mitochondrial density; (ii) a substrate switch away from fatty acids and towards other substrates such as glucose, amino acids and ketone bodies; and (iii) a shift from aerobic to anaerobic metabolism. There remains a lack of a consensus in these areas, most likely as a consequence of the variations in degree and duration of hypoxic exposure, as well as the broad range of experimental parameters used as markers of metabolic processes. To attempt to resolve some of the controversies, we performed a comprehensive review of the literature pertaining to hypoxia-induced changes in skeletal muscle energy metabolism. We found evidence that mass-specific mitochondrial function is decreased prior to mass-specific mitochondrial density, implicating intra-mitochondrial changes in the response to environmental hypoxia. This loss of oxidative capacity does not appear to be matched by a loss of glycolytic capacity, which on the whole is not altered by environmental hypoxia. Environmental hypoxia does however induce a selective attenuation of fatty acid oxidation, whilst glucose uptake is maintained or increased, perhaps to support glycolysis in the face of a downregulation of oxidative metabolism, optimising the pathways of ATP synthesis for the hypoxic environment.

摘要

骨骼肌会因环境缺氧而发生代谢重塑,然而这一过程的某些方面仍存在争议。一般来说,环境缺氧被认为会导致:(i)线粒体密度降低;(ii)底物从脂肪酸转向其他底物,如葡萄糖、氨基酸和酮体;(iii)从有氧代谢转变为无氧代谢。这些领域仍缺乏共识,很可能是由于缺氧暴露的程度和持续时间不同,以及用作代谢过程标志物的实验参数范围广泛所致。为了试图解决一些争议,我们对与缺氧诱导的骨骼肌能量代谢变化相关的文献进行了全面综述。我们发现有证据表明,在质量特异性线粒体密度降低之前,质量特异性线粒体功能就已下降,这表明线粒体内部的变化参与了对环境缺氧的反应。氧化能力的这种丧失似乎并未伴随着糖酵解能力的丧失,总体而言,糖酵解能力不会因环境缺氧而改变。然而,环境缺氧确实会导致脂肪酸氧化的选择性减弱,同时葡萄糖摄取维持不变或增加,这可能是为了在氧化代谢下调的情况下支持糖酵解,从而为缺氧环境优化ATP合成途径。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a8b6/4253994/1c87c0dfbd51/13728_2014_67_Fig1_HTML.jpg

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