KEY POINTS: Dietary nitrate supplementation increases plasma nitrite concentration, which provides an oxygen-independent source of nitric oxide and can delay skeletal muscle fatigue. Nitrate supplementation has been shown to increase myofibre calcium release and force production in mouse skeletal muscle during contractions at a supra-physiological oxygen tension, but it is unclear whether nitrite exposure can delay fatigue development and improve myofibre calcium handling at a near-physiological oxygen tension. Single mouse muscle fibres acutely treated with nitrite had a lower force and cytosolic calcium concentration during single non-fatiguing contractions at a near-physiological oxygen tension. Nitrite treatment delayed fatigue development during repeated fatiguing isometric contractions at near-physiological, but not at supra-physiological, oxygen tension in combination with better maintenance of myofilament calcium sensitivity and sarcoplasmic reticulum calcium pumping. These findings improve understanding of the mechanisms by which increased skeletal muscle nitrite exposure might be ergogenic and imply that this is related to improved calcium handling.
ABSTRACT: Dietary nitrate (NO) supplementation, which increases plasma nitrite (NO) concentration, has been reported to attenuate skeletal muscle fatigue development. Sarcoplasmic reticulum (SR) calcium (Ca) release is enhanced in isolated single skeletal muscle fibres following NOsupplementation or NOincubation at a supra-physiologicalbut it is unclear whether NOincubation can alter Cahandling and fatigue development at a near-physiological. We hypothesised that NOtreatment would improve Cahandling and delay fatigue at a physiologicalin intact single mouse skeletal muscle fibres. Each muscle fibre was perfused with Tyrode solution pre-equilibrated with either 20% (∼150 Torr) or 2% O( = 15.6 Torr) in the absence and presence of 100 µM NaNO. At supra-physiological(i.e. 20% O), time to fatigue was lowered by 34% with NaNO(control: 257 ± 94 vs. NaNO: 159 ± 46 s, Cohen's d = 1.63, P < 0.05), but extended by 21% with NaNOat 2% O(control: 308 ± 217 vs. NaNO: 368 ± 242 s, d = 1.14, P < 0.01). During the fatiguing contraction protocol completed with NaNOat 2% O, peak cytosolic Caconcentration ([Ca]) was not different (P > 0.05) but [Ca]accumulation between contractions was lower, concomitant with a greater SR Capumping rate (P < 0.05) compared to the control condition. These results demonstrate that increased exposure to NOblunts fatigue development at near-physiological, but not at supra-physiological,through enhancing SR Capumping rate in single skeletal muscle fibres. These findings extend our understanding of the mechanisms by which increased NOexposure can mitigate skeletal muscle fatigue development. 3 2 3 2 2 2 2 2 2 2 2 2 2 2 2 2c c2 2 --2+ ---2+ -2+ 2+ 2+ 2+ 2+ -2+ -P O2P O2P O2P O2P O2P O2P O2
