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Broatch, J. R.

Publications and source records attributed to Broatch, J. R..

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Regulation of Na+,K+-ATPase isoforms and phospholemman (FXYD1) in skeletal muscle fibre types by exercise training and cold-water immersion in men

Little is understood about the fibre type-dependent regulation of Na+,K+-ATPase (NKA) isoforms by exercise training in humans. The main aim of this study was therefore to assess the impact of a period of repeated exercise sessions on NKA-isoform protein abundance in different skeletal muscle fibre types in men. Post-exercise cold-water immersion (CWI) has been reported to increase oxidative stress, which may be one mechanism underlying increases in NKA-isoform expression. Thus, a second aim was to evaluate the effect of CWI on training-induced modulation of NKA-isoform abundance. Vastus lateralis muscle biopsies were obtained from nineteen men at rest before (Pre) and after (Post) six weeks of intense interval cycling, with training sessions followed by passive rest (CON, n=7) or CWI (10{degrees}C; COLD, n=5). Training increased (p<0.05) the abundance of NKA1 and NKA{beta}3 in both type I and type II fibres, NKA{beta}1 in type II fibres, but was without effect on NKA2 and NKA3 (p>0.05). Furthermore, training decreased FXYD1 protein content in type I fibres, which abolished its fibre type-specific expression detected at Pre (p<0.05). CWI was without impact on the responses to training (p>0.05). These results highlight that NKA isoforms are regulated in a fibre type-dependent fashion in response to intense training in humans. This may partly explain the improvement in muscle Na+/K+ handling after a period of intense training. CWI may be performed without adversely or favourably affecting training-induced changes in NKA-isoform abundance.\n\nSummary in key pointsO_LIIt is unclear how Na+,K+-ATPase (NKA) isoforms are regulated in different skeletal muscle fibre types by exercise training in humans, and the effect on phospholemman (FXYD1) protein abundance in different fibre types remains to be elucidated. We investigated the impact of six weeks of training on NKA-isoform protein abundance (1-3, {beta}1-3 and FXYD1) in type I and II muscle fibres in men.\nC_LIO_LIWe show that intense interval training selectively increases the protein content of NKA 1 and {beta}3 in both fibre types, {beta}1 in type II fibres, and decreases FXYD1 in type I fibres.\nC_LIO_LIThese results suggest the favourable impact of intense training on human muscle Na+/K+ regulation could be attributable, in part, to fibre type-dependent modulation of NKA-isoform abundance.\nC_LIO_LIGiven that cold exposure has been shown to modulate cellular redox state, which has been linked to increased NKA expression, we also investigated the effect of exercise training plus cold-water immersion (CWI) on the fibre type-specific responses of NKA isoforms and FXYD1. We found that CWI was without effect on the responses to training.\nC_LI\n\nAbbreviationsAMPK{beta}2, 5 AMP-activated protein kinase subunit {beta}2; CaMKII, Ca2+-calmodulin-dependent protein kinase isoform 2; COLD, cold-water immersion group; CON, control group; Ct, cycle threshold; CV, coefficient of variation; CWI, cold-water immersion; EDL, extensor digitorum longus; FXYD1, phospholemman isoform 1; HSP70, heat-shock protein 70; GXT, graded exercise test; K+, potassium; Km, Michaelis-Menten constant; MHC, myosin heavy chain; Na+, sodium; NF-1, neurofibromatosis type 1; NKA, Na+,K+-ATPase; ROS, reactive oxygen species; SDS-PAGE, sodium dodecyl sulphate polyacrylamide gel electrophoresis; SERCA1, sarco/endoplasmic reticulum Ca2+-ATPase isoform 1; VO2peak, maximum oxygen uptake.

physiology

Post-exercise cold-water immersion increases Na+,K+-ATPase α2-isoform mRNA content in parallel with elevated Sp1 expression in human skeletal muscle

We investigated the effect of a session of sprint-interval exercise on the mRNA content of NKA isoforms (1-3, {beta}1-3) and FXYD1 in human skeletal muscle. To explore some of the cellular stressors involved in this regulation, we evaluated the association between these mRNA responses and those of the transcription factors Sp1, Sp3 and HIF-1. Given cold exposure perturbs muscle redox homeostasis, which may be one mechanism important for increases in NKA-isoform mRNA, we also explored the effect of post-exercise cold-water immersion (CWI) on the mRNA responses. Muscle was sampled from nineteen men before (Pre) and after (+0h, +3h) exercise plus passive rest (CON, n=10) or CWI (10{degrees}C; COLD, n=9). In COLD, exercise increased NKA2 and Sp1 mRNA (+0h, p<0.05). These genes remained unchanged in CON (p>0.05). In both conditions, exercise increased NKA1, NKA{beta}3 and HIF-1 mRNA (+3h; p <0.05), decreased NKA{beta}2 mRNA (+3h; p<0.05), whereas NKA3, NKA{beta}1, FXYD1 and Sp3 mRNA remained unchanged (p>0.05). These human findings highlight 1) sprint-interval exercise increases the mRNA content of NKA 1 and {beta}3, and decreases that of NKA {beta}2, which may relate, in part, to exercise-induced muscle hypoxia, and 2) post-exercise CWI augments NKA2 mRNA, which may be associated with promoted Sp1 activation.

physiology