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Post‐exercise intramuscular O<sub>2</sub> supply is tightly coupled with a higher proximal‐to‐distal ATP synthesis rate in human tibialis anterior

17

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50

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2020

Year

Abstract

Phosphorus magnetic resonance spectroscopy (<sup>31</sup> P MRS) of human tibialis anterior (TA) revealed a strong proximo-distal gradient in the post-exercise phosphocreatine (PCr) recovery rate constant (k<sub>PCr</sub> ), a measure of muscle oxidative capacity. The aim of this study was to investigate whether this k<sub>PCr</sub> gradient is related to O<sub>2</sub> supply, resting phosphorylation potential, muscle fibre type, or type of exercise. Fifteen male volunteers performed continuous isometric ankle dorsiflexion at 30% maximum force until exhaustion. At multiple locations along the TA, we measured the oxidative PCr resynthesis rate (V<sub>PCr</sub> = k<sub>PCr</sub> × PCr depletion) by <sup>31</sup> P MRS, the oxyhaemoglobin recovery rate constant (k<sub>O2Hb</sub> ) by near infrared spectroscopy, and muscle perfusion with MR intravoxel incoherent motion imaging. The k<sub>O2Hb</sub> , k<sub>PCr</sub> , V<sub>PCr</sub> and muscle perfusion depended on measurement location (P < 0.001, P < 0.001, P = 0.032 and P = 0.003, respectively), all being greater proximally. The k<sub>O2Hb</sub> and muscle perfusion correlated with k<sub>PCr</sub> (r = 0.956 and r = 0.852, respectively) and V<sub>PCr</sub> (r = 0.932 and r = 0.985, respectively), the latter reflecting metabolic O<sub>2</sub> consumption. Resting phosphorylation potential (PCr/inorganic phosphate) was also higher proximally (P < 0.001). The surrogate for fibre type, carnosine content measured by <sup>1</sup> H MRS, did not differ between distal and proximal TA (P = 0.884). Performing intermittent exercise to avoid exercise ischaemia, still led to larger k<sub>PCr</sub> proximally than distally (P = 0.013). In conclusion, the spatial k<sub>PCr</sub> gradient is strongly associated with the spatial variation in O<sub>2</sub> supply. It cannot be explained by exercise-induced ischaemia nor by fibre type. Our findings suggest it is driven by a higher proximal intrinsic mitochondrial oxidative capacity, apparently to support contractile performance of the TA.

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