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Effects of hypoxia on cerebral and muscle haemodynamics during knee extensions in healthy subjects
Authors:Paulo Sergio Chagas Gomes  Cristiane Matsuura  Yagesh N. Bhambhani
Affiliation:1. Laboratório Crossbridges, Programa de Pós-gradua??o em Ciências do Exercício e do Esporte, Universidade Gama Filho, Rua Manoel Vitorino 553, Piedade, Rio de Janeiro, RJ, 20748-900, Brazil
2. Instituto de Biologia, Universidade do Estado do Rio de Janeiro, Rio de Janeiro, Brazil
3. Faculty of Rehabilitation Medicine, University of Alberta, Edmonton, Canada
Abstract:A hypoxic model was used to investigate changes in localized cerebral and muscle haemodynamics during knee extension (KE) in healthy individuals. Thirty-one young healthy volunteers performed one set of KE until failure under hypoxia (14 % O2) or normoxia (21 % O2) at 50, 75 or 100 % of 1 repetition maximum, in random order, on three occasions. Prefrontal cerebral and vastus lateralis muscle oxygenation and blood volume (Cox, Mox, Cbv and Mbv, respectively) were recorded simultaneously by near-infrared spectroscopy. Hypoxia induced significant declines in Cox [?0.017 ± 0.016 optical density (OD) units] and Mox (?0.014 ± 0.026 OD units) and increases in Cbv (0.017 ± 0.027 OD units) and Mbv (0.016 ± 0.023 OD units) at rest. Hypoxia significantly reduced total work (TW) performed during KE at each exercise intensity. Cox, Cbv, Mox, and Mbv changes during KE did not differ between normoxia and hypoxia. Correlations between TW done and Cox changes under normoxia (r = 0.04, p = 0.182) and hypoxia (r = 0.05, p = 0.122) were not significant. However, TW was significantly correlated with Mox under both normoxia (R 2 = 0.24, p = 0.000) and hypoxia (R 2 = 0.15, p = 0.004). Since changes in Cox and Mox reflect alterations in the balance between oxygen delivery and extraction in these tissues, which, in the brain, is an index of neuronal activation, we conclude that: (1) limitation of KE performance was mediated peripherally under both normoxia and hypoxia, with no additional effect of hypoxia, and (2) because of the low common variance with Mox additional intramuscular factors likely play a role in limiting KE performance.
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