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Effect of acute environmental hypoxia on protein metabolism in human skeletal muscle

Title: Effect of acute environmental hypoxia on protein metabolism in human skeletal muscle
Authors: D'Hulst, G.; Jamart, C.; Van Thienen, R.; Hespel, P.; Francaux, M.; Deldicque, L.
Source: Acta Physiologica ; volume 208, issue 3, page 251-264 ; ISSN 1748-1708 1748-1716
Publisher Information: Wiley
Publication Year: 2013
Collection: Wiley Online Library (Open Access Articles via Crossref)
Description: Hypoxia‐induced muscle wasting has been observed in several environmental and pathological conditions. However, the molecular mechanisms behind this loss of muscle mass are far from being completely elucidated, certainly in vivo . When studying the regulation of muscle mass by environmental hypoxia, many confounding factors have to be taken into account, such as decreased protein ingestion, sleep deprivation or reduced physical activity, which make difficult to know whether hypoxia per se causes a reduction in muscle mass. Aim We hypothesized that acute exposure to normobaric hypoxia (11% O 2 ) would repress the activation of the mTOR pathway usually observed after a meal and would activate the proteolytic pathways in skeletal muscle. Methods Fifteen subjects were exposed passively for 4 h to normoxic and hypoxic conditions in a random order after consumption of a light breakfast. A muscle biopsy and a blood sample were taken before, after 1 and 4 h of exposure. Results After 4 h, plasma insulin concentration and the phosphorylation state of PKB and S6K1 in skeletal muscle were higher in hypoxia than in normoxia ( P < 0.05). At the same time, Redd1 mRNA level was upregulated ( P < 0.05), whilst MAFbx mRNA decreased ( P < 0.05) in hypoxia compared with normoxia. Proteasome, cathepsin L and calpain activities were not altered by environmental hypoxia. Conclusion Contrary to our hypothesis and despite an increase in the mRNA level of Redd1, an inhibitor of the mTORC 1 pathway, short‐term acute environmental hypoxia induced a higher response of PKB and S6K1 to a meal, which may be due to increased plasma insulin concentration.
Document Type: article in journal/newspaper
Language: English
DOI: 10.1111/apha.12086
Availability: https://doi.org/10.1111/apha.12086; https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1111%2Fapha.12086; https://onlinelibrary.wiley.com/doi/pdf/10.1111/apha.12086
Rights: http://onlinelibrary.wiley.com/termsAndConditions#vor
Accession Number: edsbas.9F766CE0
Database: BASE