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J Appl Physiol (February 3, 2005). doi:10.1152/japplphysiol.00355.2004
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Submitted on April 1, 2004
Accepted on January 25, 2005

Relationship between Intracellular PO2 Recovery Kinetics and Fatigability in Isolated Single Frog Myocytes

Casey A. Kindig1, Brandon Walsh1, Richard A. Howlett1*, Creed M. Stary1, and Michael C. Hogan1

1 Department of Medicine, Physiology Division, University of California-San Diego, La Jolla, CA, USA

* To whom correspondence should be addressed. E-mail: rhowlett{at}ucsd.edu.

In single frog skeletal myocytes, a linear relationship exists between "fatigability" and oxidative capacity. The purpose of this investigation was to study the relationship between the intracellular PO2 (PIO2) offset kinetics and fatigability in single Xenopus laevis myocytes in order to test the hypothesis that PIO2 offset kinetics would be related linearly with myocyte fatigability and, by inference, oxidative capacity. Individual myocytes (n=30) isolated from lumbrical muscle were subjected to a 2-min bout of isometric peak tetanic contractions at either 0.25 or 0.33 Hz frequency while PIO2 was measured continuously via phosphorescence quenching techniques. The mean response time (MRT; time to 63% of the overall response) for PIO2 recovery from contracting values to resting baseline was calculated. Following the initial square-wave constant frequency contraction trial, each cell performed an incremental contraction protocol (i.e., frequency increase every 2-min from 0.167, 0.25, 0.33, 0.5, 1.0, 2.0 Hz until peak tension fell below 50% of initial values [TTF]). TTF values ranged from 3.39 to 10.04 min for the myocytes. The PIO2 recovery MRT ranged from 26 to 146 s. A significant (p<0.05), negative relationship (MRT = -12.68TTF + 168.3, r2 = 0.605) between TTF and PIO2 recovery MRT existed. These data demonstrate a significant correlation between fatigability and oxidative phosphorylation recovery kinetics consistent with the notion that oxidative capacity determines, in part, the speed with which skeletal muscle can recover energetically to alterations in metabolic demand.




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