## Abstract The forward and reverse rates through the creatineβkinase (CK) catalyzed reaction, phosphocreatine + ADP + H^+^ \documentclass{article}\pagestyle{empty}\begin{document}$\'\mathop \mathbin{\lower.3ex\hbox{$\buildrel\textstyle\rightarrow\over {\smash{\leftarrow}\vphantom{\_{\vbox to.5ex{\
31P magnetization transfer studies of creatine kinase kinetics in living rabbit brain
β Scribed by Hadessa Degani; Jeffery R. Alger; Robert G. Shulman; Ognen A. C. Petroff; James W. Prichard
- Publisher
- John Wiley and Sons
- Year
- 1987
- Tongue
- English
- Weight
- 616 KB
- Volume
- 5
- Category
- Article
- ISSN
- 0740-3194
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β¦ Synopsis
The kinetics of the CK reaction in the living rabbit brain was studied by three 31P magnetization transfer methods: inversion recovery (IR), inversion transfer (IT), and steady-state saturation transfer (SSST). Longitudinal relaxation rates (tau -1) were determined from IR and IT experiments. The values were 0.88 +/- 0.08 s-1 for PCr and 2.45 +/- 0.39 s-1 for gamma-ATP. Analysis of the results of SSST experiments in which gamma-ATP was saturated yielded a forward rate constant kF of 0.53 +/- 0.07 s-1. Upon saturation of PCr no change in the gamma-ATP signal could be detected in SSST. An average reverse rate constant (kR +/- S.D.) of 0.52 +/- 0.04 s-1 was estimated by analyzing IT data from three experiments with selective inversion of gamma-ATP. The standard error of kR was 50%. The average [PCr]/[ATP] of 1.21 +/- 0.16 together with the values of kF and kR yielded a forward-to-reverse flux ratio of 1.23. Within our limits of accuracy this ratio was not significantly different from 1.0, thus suggesting that in the brain the forward and reverse CK fluxes are equal.
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
## Abstract ^31^P magnetic resonance spectroscopy was used to investigate changes in high energy phosphate levels and creatine kinase (CK) kinetics induced in the human visual cortex during photic stimulation. CK kinetics was evaluated by measuring the apparent unidirectional rate constant (__k__~f
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