## Abstract The creatine kinase reaction has been studied by ^31^P NMR in exercising human calf muscle. Quantitative analysis of high energy phosphates and saturation transfer study of the creatine kinase flux in the direction of ATP synthesis (__V__~for~) were performed at rest and during exercise
Creatine loading and resting skeletal muscle phosphocreatine flux: a saturation-transfer NMR study
β Scribed by Wiedermann, D
- Book ID
- 104390803
- Publisher
- Springer
- Year
- 2001
- Tongue
- English
- Weight
- 154 KB
- Volume
- 13
- Category
- Article
- ISSN
- 0968-5243
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β¦ Synopsis
31
P saturation-transfer nuclear magnetic resonance spectroscopy was used to study skeletal muscle phosphocreatine (PCr) flux in healthy male volunteers. Data analysis included consideration of effects from incomplete saturation and radiofrequency spillover. Spectra were recorded from the resting gastrocnemius muscle before and after 6 days of creatine monohydrate (Crβ’H 2 O) intake (20 g/day). Parallel to an improved muscle performance during maximal intermittent exercise following Crβ’H 2 O supplementation, the concentration of PCr increased (P= 0.01) by 23% (34.9 9 2.8 mmol/l vs. 28.6 9 2.7 mmol/l), whereas other metabolites were unaffected (inorganic phosphate: 4.3 9 1.4 mmol/l, free intracellular Mg 2 + : 1.190.7 mmol/l, cytosolic pH: 7.049 0.02). Forward and reverse fluxes through the creatine kinase (CK) reaction did not change significantly from their baseline levels (6 for : 11.8 95.4 mmol/l per second vs. 15.3 96.8 mmol/l per second, (6 rev : 9.59 3.4 mmol/l per second vs. 10.9 9 3.7 mmol/l per second). The rate of PCr resynthesis in resting muscle is not limited by the CK reaction, which is near equilibrium. Consequently, the post-load increase in total creatine has no effect on the unidirectional CK reaction rates.
π SIMILAR VOLUMES
The steady-state kinetics of the creatine kinase reaction in rabbit skeletal muscle in vivo was investigated using inversion and saturation magnetization transfer techniques. Both techniques determined the forward rate of this reaction (creatine phosphate ATP) as approximately 0.3 s-1. This correspo
Off-resonance saturation caused a reduction of the 3.04 ppm NMR signal from the methyl protons of creatine in rat hindleg skeletal muscle. 1 H-NMR spectra were recorded over a 200 kHz range of off-resonance saturation frequencies. The span of frequencies over which the creatine signal was reduced gr