First published online August 4, 2005
Journal of Experimental Biology 208, 3159-3167 (2005)
Published by The Company of Biologists 2005
doi: 10.1242/jeb.01703
Cost of transport is increased after cold exposure in Monodelphis domestica: training for inefficiency
Paul J. Schaeffer1,2,*,
Jason J. Villarin1,
,
David J. Pierotti1,
Daniel P. Kelly2,3 and
Stan L. Lindstedt1
1 Department of Biological Sciences, Physiology and Functional Morphology
Group, Northern Arizona University, Flagstaff, AZ 86011, USA
2 Center for Cardiovascular Research and Department of Medicine, Washington
University School of Medicine, St Louis, MO 63110, USA
3 Department of Molecular Biology and Pharmacology, and Department of
Pediatrics, Washington University School of Medicine, St Louis, MO 63110,
USA

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Fig. 1. Cost of transport during locomotion. Using an open flow metabolic system,
O2 was measured
as a function of running speed on a motorized treadmill. The cold-acclimated
animals had significantly higher O2 utilization as a function of
speed such that on average 15% more oxygen was consumed while running at the
same speed as thermoneutral controls. Values are means ±
S.E.M. at each speed. CS, cold, sedentary;
CT, cold, trained; TnS, thermoneutral, sedentary; TnT, thermoneutral,
trained.
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Fig. 2. Kinetics of single twitch contractions. (A) Time to peak tension per gram
of force produced (TPTg) for single twitches of the semitendinosus
muscle by the four experimental groups (as in
Table 1) was significantly
increased by cold acclimation but not by exercise training. There is a trend
for increased time required to generate force with either the TnT or CS
treatment group, but only those animals subjected to both treatments (CT)
showed a statistically significant slowing of twitch speed. (B) Half
relaxation time per gram of force produced ( RTg) for single
twitches by semitendinosus muscles of the four experimental groups. The
RTg was significantly longer in cold-acclimated but not by
exercise-trained animals. Both cold groups had a longer relaxation rate;
however, post-hoc pairwise comparison showed this effect was only
statistically significant in the CT group. Values are means ±
S.E.M. and different superscripted letters
indicate significant pairwise differences between groups. CS, cold, sedentary;
CT, cold, trained; TnS, thermoneutral, sedentary; TnT, thermoneutral,
trained.
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Fig. 3. Maximal shortening velocity. Maximal muscle shortening velocity
(vmax, muscle lengths ML s1)
was significantly lower following both cold acclimation and exercise training.
The extent of the effect tended to increase more with cold acclimation than
with exercise training. Values are means ±
S.E.M. and different superscripted letters
indicate significant pairwise differences between groups. CS, cold, sedentary;
CT, cold, trained; TnS, thermoneutral, sedentary; TnT, thermoneutral,
trained.
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Fig. 4. Fatigue index. The fatigue index is a measure of the percent of force
production capacity remaining after a fatiguing series of contractions, and is
thus a measure of muscle endurance. The fatigue index of semitendinosus
muscles from the four groups was significantly increased only by cold
acclimation, and the CT group showed the highest resistance to fatigue. Values
are means ± S.E.M. and different
superscripted letters indicate significant pairwise differences between
groups. CS, cold, sedentary; CT, cold, trained; TnS, thermoneutral, sedentary;
TnT, thermoneutral, trained.
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Fig. 5. Monodelphis domestica UCP-3 expression. The expression of the mRNA
encoding a putative homolog of uncoupling protein 3 (Md-UCP3) was induced in
hindlimb skeletal muscle of cold-acclimated animals, as detected by northern
blot. Intensity of 28S RNA, stained with Ethidium Bromide, is included as a
loading control.
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© The Company of Biologists Ltd 2005