Phosphocreatine kinetics at the onset of contractions in skeletal muscle of MM creatine kinase knockout mice

被引:35
作者
Roman, BB
Meyer, RA
Wiseman, RW
机构
[1] Michigan State Univ, Dept Physiol, Mol Imaging Res Ctr, E Lansing, MI 48824 USA
[2] Michigan State Univ, Dept Radiol, Mol Imaging Res Ctr, E Lansing, MI 48824 USA
[3] Univ Illinois, Med Ctr, Dept Cardiol, Chicago, IL USA
来源
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY | 2002年 / 283卷 / 06期
关键词
skeletal muscle energetics; metabolic modeling; phosphorus nuclear magnetic resonance spectroscopy; phosphocreatine;
D O I
10.1152/ajpcell.00210.2002
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Phosphocreatine (PCr) depletion during isometric twitch stimulation at 5 Hz was measured by P-31-NMR spectroscopy in gastrocnemius muscles of pentobarbital-anesthetized MM creatine kinase knockout (MMKO) vs. wild-type C57B (WT) mice. PCr depletion after 2 s of stimulation, estimated from the difference between spectra gated to times 200 ms and 140 s after 2-s bursts of contractions, was 2.2 +/- 0.6% of initial PCr in MMKO muscle vs. 9.7 +/- 1.6% in WT muscles (mean +/- SE, n = 7, P < 0.001). Initial PCr/ATP ratio and intracellular pH were not significantly different between groups, and there was no detectable change in intracellular pH or ATP in either group after 2 s. The initial difference in net PCr depletion was maintained during the first minute of continuous 5-Hz stimulation. However, there was no significant difference in the quasi-steadystate PCr level approached after 80 s (MMKO 36.1 +/- 3.5 vs. WT 35.5 +/- 4.4% of initial PCr; n = 5-6). A kinetic model of ATPase, creatine kinase, and adenylate kinase fluxes during stimulation was consistent with the observed PCr depletion in MMKO muscle after 2 s only if ADP-stimulated oxidative phosphorylation was included in the model. Taken together, the results suggest that cytoplasmic ADP more rapidly increases and oxidative phosphorylation is more rapidly activated at the onset of contractions in MMKO compared with WT muscles.
引用
收藏
页码:C1776 / C1783
页数:8
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