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J Appl Physiol 101: 477-485, 2006. First published April 6, 2006; doi:10.1152/japplphysiol.00042.2006
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Maximal oxygen consumption in relation to subordinate traits in lines of house mice selectively bred for high voluntary wheel running

Enrico L. Rezende, Fernando R. Gomes, Jessica L. Malisch, Mark A. Chappell, and Theodore Garland, Jr.

Department of Biology, University of California, Riverside, California

Submitted 13 January 2006 ; accepted in final form 27 March 2006

We studied relations between maximal O2 consumption (VO2 max) during forced exercise and subordinate traits associated with blood O2 transport and cellular respiration in four lines of mice selectively bred for high voluntary wheel running (S lines) and their four nonselected control (C) lines. Previously, we reported VO2 max of 59 females at three PO2 (hypoxia = 14% O2, normoxia = 21%, hyperoxia = 30%). Here, we test the hypothesis that variation in VO2 max can be explained, in part, by hemoglobin concentration and PO2 necessary to obtain 50% O2 saturation of Hb (an estimate of Hb affinity for O2) of the blood as well as citrate synthase activity and myoglobin concentration of ventricles and gastrocnemius muscle. Statistical analyses controlled for body mass, compared S and C lines, and also considered effects of the mini-muscle phenotype (present only in S lines and resulting from a Mendelian recessive allele), which reduces hindlimb muscle mass while increasing muscle mass-specific aerobic capacity. Although S lines had higher VO2 max than C, subordinate traits showed no statistical differences when the presence of the mini-muscle phenotype was controlled. However, subordinate traits did account for some of the individual variation in VO2 max. Ventricle size was a positive predictor of VO2 max at all three PO2. Blood Hb concentration was a positive predictor of VO2 max in S lines but a negative predictor in C lines, indicating that the physiological underpinnings of VO2 max have been altered by selective breeding. Mice with the mini-muscle phenotype had enlarged ventricles, with higher mass-specific citrate synthase activity and myoglobin concentration, which may account for their higher VO2 max in hypoxia.

cardiac output; experimental evolution; hemoglobin; hypoxia tolerance; myoglobin



Address for reprint requests and other correspondence: E. L. Rezende, Integrative Ecology Group, Estación Biológica Doñana, CSIC, Apdo. 1056, E-41080 Seville, Spain (e-mail: enrico.rezende{at}ebd.csic.es)




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