Journal of Applied Physiology  AJP: Regulatory, Integrative and Comparative Physiology
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J Appl Physiol (March 17, 2005). doi:10.1152/japplphysiol.00084.2005
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Submitted on January 25, 2005
Accepted on March 10, 2005

Response of XIAP, ARC, and FLIP apoptotic suppressors to 8-weeks of treadmill running in rat heart and skeletal muscle

Parco M Siu1, Randall W Bryner1, Zsolt Murlasits1, and Stephen E Alway1*

1 Laboratory of Muscle Biology and Sarcopenia, Division of Exercise Physiology, West Virginia University School of Medicine, Morgantown, WV, USA

* To whom correspondence should be addressed. E-mail: salway{at}hsc.wvu.edu.

Although it has been demonstrated that exercise training has an anti-apoptotic effect on postmitotic myocytes, the mechanisms responsible for this effect are still largely unclear. Since the anti-apoptotic effect of exercise training in postmitotic myocytes could be possibly mediated by the upregulation of apoptotic suppressors, this study examined the effect of endurance training on endogenous apoptotic suppressors including XIAP, ARC, and FLIP in skeletal and cardiac muscles. Eight adult Sprague Dawley rats were trained 5 days weekly for 8 weeks on treadmill and eight sedentary rats served as controls. Soleus and ventricle muscles were dissected 2 days after the last training session. The mRNA content of XIAP, ARC, and FLIP was estimated by RT-PCR with ribosomal 18S RNA used as an internal control. The protein expression of XIAP, ARC, FLIPS and FLIP{alpha} was assessed by Western immunoblot. Following training, mRNA content of ARC and FLIP was not different between the control and trained animals whereas XIAP mRNA content was elevated by 22% and 14% in the trained soleus and cardiac muscles, respectively, relative to the control samples. No difference was found in the protein content of FLIPS and FLIP{alpha} between control and trained muscles while XIAP and ARC protein content was increased by 18% and 38%, correspondingly, in the soleus muscle of trained animals. Furthermore, negative relationships were found between XIAP and apoptotic DNA fragmentation as well as ARC and caspase-3 activity. These findings are consistent with the hypothesis that the modulation of apoptotic suppressors is involved in training-induced attenuation of apoptosis in skeletal and cardiac muscles.




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