Aerobic exercise training improves skeletal muscle function and Ca(2+) handling-related protein expression in sympathetic hyperactivity-induced heart failure


Autoria(s): Bueno Junior, C. R.; Ferreira, J. C. B.; Pereira, M. G.; Bacurau, Aline Villa Nova; Brum, Patricia Chakur
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

18/10/2012

18/10/2012

2010

Resumo

Bueno CR Jr, Ferreira JC, Pereira MG, Bacurau AV, Brum PC. Aerobic exercise training improves skeletal muscle function and Ca(2+) handling-related protein expression in sympathetic hyperactivity-induced heart failure. J Appl Physiol 109: 702-709, 2010. First published July 1, 2010; doi: 10.1152/japplphysiol.00281.2010.-The cellular mechanisms of positive effects associated with aerobic exercise training on overall intrinsic skeletal muscle changes in heart failure (HF) remain unclear. We investigated potential Ca(2+) abnormalities in skeletal muscles comprising different fiber compositions and investigated whether aerobic exercise training would improve muscle function in a genetic model of sympathetic hyperactivity-induced HF. A cohort of male 5-mo-old wild-type (WT) and congenic alpha(2A)/alpha(2C) adrenoceptor knockout (ARKO) mice in a C57BL/6J genetic background were randomly assigned into untrained and trained groups. Exercise training consisted of a 8-wk running session of 60 min, 5 days/wk (from 5 to 7 mo of age). After completion of the exercise training protocol, exercise tolerance was determined by graded treadmill exercise test, muscle function test by Rotarod, ambulation and resistance to inclination tests, cardiac function by echocardiography, and Ca(2+) handling-related protein expression by Western blot. alpha(2A)/alpha(2C)ARKO mice displayed decreased ventricular function, exercise intolerance, and muscle weakness paralleled by decreased expression of sarcoplasmic Ca(2+) release-related proteins [alpha(1)-, alpha(2)-, and beta(1)-subunits of dihydropyridine receptor (DHPR) and ryanodine receptor (RyR)] and Ca(2+) reuptake-related proteins [sarco(endo) plasmic reticulum Ca(2+)-ATPase (SERCA) 1/2 and Na(+)/Ca(2+) exchanger (NCX)] in soleus and plantaris. Aerobic exercise training significantly improved exercise tolerance and muscle function and reestablished the expression of proteins involved in sarcoplasmic Ca(2+) handling toward WT levels. We provide evidence that Ca(2+) handling-related protein expression is decreased in this HF model and that exercise training improves skeletal muscle function associated with changes in the net balance of skeletal muscle Ca(2+) handling proteins.

Fundacao de Amparo a Pesquisa do Estado de Sao Paolo-Brasil (FAPESP)[05/59740-7]

Fundacao de Amparo a Pesquisa do Estado de Sao Paolo-Brasil (FAPESP)[06/57836-0R]

Fundacao de Amparo a Pesquisa do Estado de Sao Paolo-Brasil (FAPESP)[2009/03143-1]

Fundacao de Amparo a Pesquisa do Estado de Sao Paolo-Brasil (FAPESP)[2008/50777-3]

Conselho Nacional de Pesquisa e Desenvolvimento-Brasil (CNPq)[BPQ 301519/2008-0]

Identificador

JOURNAL OF APPLIED PHYSIOLOGY, v.109, n.3, p.702-709, 2010

8750-7587

http://producao.usp.br/handle/BDPI/17318

10.1152/japplphysiol.00281.2010

http://dx.doi.org/10.1152/japplphysiol.00281.2010

Idioma(s)

eng

Publicador

AMER PHYSIOLOGICAL SOC

Relação

Journal of Applied Physiology

Direitos

restrictedAccess

Copyright AMER PHYSIOLOGICAL SOC

Palavras-Chave #cardiac diseases #muscular abnormalities #treadmill running #Ca(2+) transient #GENETIC MODEL #MYOCARDIAL-INFARCTION #CARDIAC DYSFUNCTION #MICE #RATS #ABNORMALITIES #INTOLERANCE #CAPACITY #FATIGUE #FLOW #Physiology #Sport Sciences
Tipo

article

original article

publishedVersion