Differential expression of stress proteins in rat myocardium after free wheel or treadmill run training

Citation
Eg. Noble et al., Differential expression of stress proteins in rat myocardium after free wheel or treadmill run training, J APP PHYSL, 86(5), 1999, pp. 1696-1701
Citations number
31
Categorie Soggetti
Physiology
Journal title
JOURNAL OF APPLIED PHYSIOLOGY
ISSN journal
87507587 → ACNP
Volume
86
Issue
5
Year of publication
1999
Pages
1696 - 1701
Database
ISI
SICI code
8750-7587(199905)86:5<1696:DEOSPI>2.0.ZU;2-W
Abstract
High intensity treadmill exercise increases the expression of a cardioprote ctive, inducible 72-kDa stress protein (SP72) in cardiac muscle. This inves tigation examined whether voluntary free wheel exercise training would be s ufficient to confer a similar response. Male Sprague-Dawley rats were rando mly assigned to either treadmill (TM-Tr) or free wheel (FW-Tr) training gro ups. By the end of the 8-wk training period, TM-Tr animals ran 1 h/day, 5 d ays/wk up a 10% grade, covering a distance of 8,282 m/wk. FW-Tr rats ran, o n average, 5,300 m/wk, with one-third of the animals covering distances sim ilar to those for the TM-Tr group. At the time of death, hearts of trained and caged sedentary control (Sed) animals were divided into left (LV) and r ight (RV) ventricles. Citrate synthase activity and the relative immunoblot contents of SP72, SP73 (the constitutive isoform of the SP70 family), and a 75-kDa mitochondrial chaperone (SP75) were subsequently determined. LV an d RV did not differ on any measure, and SP73, SP75, and citrate synthase we re not affected by training. Cardiac SP72 levels were elevated over fourfol d in both ventricles of TM-Tr compared with RV of FW-Sed rats. Despite the animals having run a similar total distance, cardiac SP72 content in FW-Tr rats was not different from that in Sed animals. These data indicate that v oluntary exercise training is insufficient to elicit an elevation of SP72 i n rat heart and suggest that exercise intensity may be a critical factor in evoking the cardioprotective SP72 response.