Cycling with blood flow restriction improves performance and muscle K+ regulation and alters the effect of anti-oxidant infusion in humans

被引:60
作者
Christiansen, Danny [1 ,2 ]
Eibye, Kasper H. [1 ]
Rasmussen, Villads [1 ]
Voldbye, Hans M. [1 ]
Thomassen, Martin [1 ]
Nyberg, Michael [1 ]
Gunnarsson, Thomas G. P. [1 ]
Skovgaard, Casper [1 ]
Lindskrog, Mads S. [1 ]
Bishop, David J. [2 ,3 ]
Hostrup, Morten [1 ]
Bangsbo, Jens [1 ]
机构
[1] Univ Copenhagen, Dept Nutr Exercise & Sports NEXS, Sect Integrat Physiol, DK-2100 Copenhagen O, Denmark
[2] Victoria Univ, Inst Hlth & Sport IHES, Melbourne, Vic, Australia
[3] Edith Cowan Univ, Sch Med & Hlth Sci, Perth, WA, Australia
来源
JOURNAL OF PHYSIOLOGY-LONDON | 2019年 / 597卷 / 09期
关键词
Blood flow restriction training; human muscle; antioxidant; reactive oxygen species; N-acetylcysteine; fibre type; single fibre; Na+; K+-ATPase; ion transport; N-ACETYLCYSTEINE INFUSION; RAT SKELETAL-MUSCLE; REACTIVE OXYGEN; INTENSE EXERCISE; FXYD1; PHOSPHORYLATION; ION-TRANSPORT; NA+; ATPASE; FATIGUE; ENDURANCE;
D O I
10.1113/JP277657
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Key points Training with blood flow restriction (BFR) is a well-recognized strategy for promoting muscle hypertrophy and strength. However, its potential to enhance muscle function during sustained, intense exercise remains largely unexplored. In the present study, we report that interval training with BFR augments improvements in performance and reduces net K+ release from contracting muscles during high-intensity exercise in active men. A better K+ regulation after BFR-training is associated with an elevated blood flow to exercising muscles and altered muscle anti-oxidant function, as indicated by a higher reduced to oxidized glutathione (GSH:GSSG) ratio, compared to control, as well as an increased thigh net K+ release during intense exercise with concomitant anti-oxidant infusion. Training with BFR also invoked fibre type-specific adaptations in the abundance of Na+,K+-ATPase isoforms (alpha(1), beta(1), phospholemman/FXYD1). Thus, BFR-training enhances performance and K+ regulation during intense exercise, which may be a result of adaptations in anti-oxidant function, blood flow and Na+,K+-ATPase-isoform abundance at the fibre-type level. We examined whether blood flow restriction (BFR) augments training-induced improvements in K+ regulation and performance during intense exercise in men, and also whether these adaptations are associated with an altered muscle anti-oxidant function, blood flow and/or with fibre type-dependent changes in Na+,K+-ATPase-isoform abundance. Ten recreationally-active men (25 +/- 4 years, 49.7 +/- 5.3 mL kg(-1) min(-1)) performed 6 weeks of interval cycling, where one leg trained without BFR (control; CON-leg) and the other trained with BFR (BFR-leg, pressure: similar to 180 mmHg). Before and after training, femoral arterial and venous K+ concentrations and artery blood flow were measured during single-leg knee-extensor exercise at 25% (Ex1) and 90% of thigh incremental peak power (Ex2) with i.v. infusion of N-acetylcysteine (NAC) or placebo (saline) and a resting muscle biopsy was collected. After training, performance increased more in BFR-leg (23%) than in CON-leg (12%, P < 0.05), whereas K+ release during Ex2 was attenuated only from BFR-leg (P < 0.05). The muscle GSH:GSSG ratio at rest and blood flow during exercise was higher in BFR-leg than in CON-leg after training (P < 0.05). After training, NAC increased resting muscle GSH concentration and thigh net K+ release during Ex2 only in BFR-leg (P < 0.05), whereas the abundance of Na+,K+-ATPase-isoform alpha(1) in type II (51%), beta(1) in type I (33%), and FXYD1 in type I (108%) and type II (60%) fibres was higher in BFR-leg than in CON-leg (P < 0.05). Thus, training with BFR elicited greater improvements in performance and reduced thigh K+ release during intense exercise, which were associated with adaptations in muscle anti-oxidant function, blood flow and Na+,K+-ATPase-isoform abundance at the fibre-type level.
引用
收藏
页码:2421 / 2444
页数:24
相关论文
共 54 条
[1]  
Abe T, 2010, J SPORT SCI MED, V9, P452
[2]   MAXIMAL PERFUSION OF SKELETAL-MUSCLE IN MAN [J].
ANDERSEN, P ;
SALTIN, B .
JOURNAL OF PHYSIOLOGY-LONDON, 1985, 366 (SEP) :233-249
[3]   Glutathione: new roles in redox signaling for an old antioxidant [J].
Aquilano, Katia ;
Baldelli, Sara ;
Ciriolo, Maria R. .
FRONTIERS IN PHARMACOLOGY, 2014, 5
[4]   Muscle oxygen kinetics at onset of intense dynamic exercise in humans [J].
Bangsbo, J ;
Krustrup, P ;
González-Alonso, J ;
Boushel, R ;
Saltin, B .
AMERICAN JOURNAL OF PHYSIOLOGY-REGULATORY INTEGRATIVE AND COMPARATIVE PHYSIOLOGY, 2000, 279 (03) :R899-R906
[5]   FXYD Proteins Reverse Inhibition of the Na+-K+ Pump Mediated by Glutathionylation of Its β1 Subunit [J].
Bibert, Stephanie ;
Liu, Chia-Chi ;
Figtree, Gemma A. ;
Garcia, Alvaro ;
Hamilton, Elisha J. ;
Marassi, Francesca M. ;
Sweadner, Kathleen J. ;
Cornelius, Flemming ;
Geering, Kaethi ;
Rasmussen, Helge H. .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2011, 286 (21) :18562-18572
[6]   Mechanism of oxidative damage of dog kidney Na/K-ATPase [J].
Boldyrev, A ;
Kurella, E .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1996, 222 (02) :483-487
[7]   PSYCHOPHYSICAL BASES OF PERCEIVED EXERTION [J].
BORG, GAV .
MEDICINE AND SCIENCE IN SPORTS AND EXERCISE, 1982, 14 (05) :377-381
[8]   CELLULAR ELECTROPHYSIOLOGICAL BASIS FOR OXYGEN RADICAL INDUCED ARRHYTHMIAS - A PATCH-CLAMP STUDY IN GUINEA-PIG VENTRICULAR MYOCYTES [J].
CERBAI, E ;
AMBROSIO, G ;
PORCIATTI, F ;
CHIARIELLO, M ;
GIOTTI, A ;
MUGELLI, A .
CIRCULATION, 1991, 84 (04) :1773-1782
[9]   Increased FXYD1 and PGC-1 mRNA after blood flow-restricted running is related to fibre type-specific AMPK signalling and oxidative stress in human muscle [J].
Christiansen, D. ;
Murphy, R. M. ;
Bangsbo, J. ;
Stathis, C. G. ;
Bishop, D. J. .
ACTA PHYSIOLOGICA, 2018, 223 (02)