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1 Laboratory of Cardiac Energetics, National Heart, Lung, and Blood Institute, Bethesda, Maryland 20892; and 2 Department of Human Anatomy and Cell Biology, University of Liverpool, Liverpool L69 3BX, United Kingdom
Received 14 August 1995; accepted in final form 6 September 1996.
Ryschon, T. W., J. C. Jarvis, S. Salmons, and R. S. Balaban.
High-energy phosphates and tension production in rabbit tibialis
anterior/extensor digitorum longus muscles. J. Appl. Physiol. 82(3): 1024-1029, 1997.
The effects of
repetitive muscle contraction on energy state and tension production
were studied in rabbit tibialis anterior/extensor digitorum longus
muscles that had been subjected to 90 days of continuous indirect
electrical stimulation at 10 Hz. Anesthetized chronically stimulated
and control rabbits were challenged with 15 min of stimulation at 4 and
15 tetani/min.
Pi-to-phosphocreatine (PCr) ratio
(Pi/PCr) was measured in vivo before, during, and
after acute stimulation by
31P-magnetic resonance
spectroscopy, and tension was recorded at the same time. Although
Pi/PCr was low at rest, it was
significantly higher in chronically stimulated muscle than in control
muscle (0.20 ± 0.02 vs. 0.05 ± 0.01, P < 0.05). Stimulation of control muscle for 15 min at both 4 and 15 tetani/min induced a significant rise in Pi/PCr, whereas the same
conditions in chronically stimulated muscle did not produce any
significant departure from initial levels. The tension produced by
control muscle fell to 93 ± 3% of its initial value during
stimulation at 4 tetani/min and to 61 ± 7% at 15 tetani/min,
respectively. In chronically stimulated muscle, on the other hand,
tension was potentiated above its initial level at both stimulation
rates (135 ± 15 and 138 ± 11%, respectively) and remained
significantly elevated throughout each trial. The ability of
chronically stimulated muscle to sustain high levels of activity with
minimal perturbations in Pi/PCr or
decrement in tension is attributable to cellular adaptations that
include a well-documented increase in oxidative capacity.
fatigue; chronic stimulation; 31P-magnetic resonance spectroscopy
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