Volume 28, Issue S1 1164.6
Physiology
Free Access

Effects of exercise and body temperature on eNOS, SIRT1, SIRT3 and Hsp70 expression in rat plantaris muscles (1164.6)

Taylor Hodge

Taylor Hodge

Department of Kinesiology & Health Sciences College of William & Mary, Williamsburg, VA, United States

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Joseph Starnes

Joseph Starnes

Department of Kinesiology University of North Carolina at Greensboro, Greensboro, NC, United States

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Bryan Feger

Bryan Feger

Department of Kinesiology University of North Carolina at Greensboro, Greensboro, NC, United States

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Lindsay Hixson

Lindsay Hixson

Department of Kinesiology University of North Carolina at Greensboro, Greensboro, NC, United States

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M. Brennan Harris

M. Brennan Harris

Department of Kinesiology & Health Sciences College of William & Mary, Williamsburg, VA, United States

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Abstract

Previously, we have demonstrated a dramatic increase in mitochondrial biogenesis in skeletal muscle of rats exercise trained while maintaining a constant core temperature. In this study, we explored the role of body temperature during exercise on the expression of multiple proteins (eNOS, SIRT1, SIRT3, and Hsp70) believed to play a role in mitochondrial biogenesis. Female, Sprague-Dawley rats (5 mos of age) were divided into three groups sedentary (S), exercise in 22°C room (ET), and exercise while maintaining core temperature (E). Exercised animals trained for 5 weeks on a motor-driven treadmill at 30 m/min, 60 min/day, 5 days/wk during final 2 wks. Core temperature was held constant in E by reducing room temp to 6-8°C. Plantaris cytochrome oxidase activity (μmoles O2/min/g wet wt) was significantly (P<0.05) elevated in both ET (37.00±2.10) and E (47.14±4.11) versus S (24.15±1.37) and significantly greater in E versus ET. Preliminary results reveal no significant differences in SIRT1, SIRT3, or eNOS expression in the soleus muscles of S, E, or ET. Hsp70 was significantly (P<0.05) elevated in the ET group. These data suggest that although mitochondrial biogenesis increases in this model, eNOS, SIRT1 and SIRT3 do not parallel this increase and may not play a role in this process.