Quantitative Evaluation of the First Order Creatine-Kinase Reaction Rate Constant in in vivo Shunted Ovine Heart Treated with Oxandrolone Using Magnetization Transfer 31P Magnetic Resonance Spectroscopy (MT-31P-MRS) and 1H/31P Double-Tuned Surface Coil: a Preliminary Study

2018 ◽  
Vol 22 (1) ◽  
pp. 26
Author(s):  
Bijaya Thapa ◽  
Marjanna Dahl ◽  
Eugene Kholmovski ◽  
Phillip Burch ◽  
Deborah Frank ◽  
...  
2000 ◽  
Vol 279 (2) ◽  
pp. E333-E339 ◽  
Author(s):  
A. Horská ◽  
K. W. Fishbein ◽  
J. L. Fleg ◽  
R. G. S. Spencer

Using31P magnetic resonance spectroscopy, creatine kinase (CK) reaction kinetics was assessed in the forearm flexor digitorum profundus muscle of healthy young ( n = 11, age 34.7 ± 5 yr) and older ( n = 20, age 73.5 ± 8 yr) subjects at rest, intermittent exercise at 20% maximum voluntary contraction (MVC), and 40% MVC. Exercise resulted in a significant increase in the average ratio of inorganic phosphate (Pi) to phosphocreatine (PCr) from resting values of 0.073 ± 0.031 (young) and 0.082 ± 0.037 (older) to 0.268 ± 0.140 (young, P < 0.01) and 0.452 ± 0.387 (older, P < 0.01) at 40% MVC. At 40% MVC, intracellular pH decreased significantly, from resting values of 7.08 ± 0.08 (young) and 7.08 ± 0.11 (older) to 6.84 ± 0.19 (young, P < 0.05) and to 6.75 ± 0.25 (older, P < 0.05). Average values of the pseudo-first-order reaction rate k (PCr→ATP) at rest were 0.07 ± 0.04 s−1 in the young and 0.07 ± 0.03 s−1 in the older group. At both exercise levels, the reaction rate constant increased compared with the resting value, but only the difference between the resting value and the 20% MVC value, which showed an 86% higher reaction rate constant in both groups, reached statistical significance ( P < 0.05). No difference in the reaction rate constant between the young and older groups was observed at either exercise level. As with k (PCr→ATP), the average phosphorus flux through the CK reaction increased during exercise at 20% MVC ( P < 0.05 in the older group) but decreased toward resting values at 40% MVC in both groups. The data in our study suggest that normal aging does not significantly affect the metabolic processes associated with the CK reaction.


2017 ◽  
Vol 30 (12) ◽  
pp. e3786 ◽  
Author(s):  
Charlie Y. Wang ◽  
Yuchi Liu ◽  
Shuying Huang ◽  
Mark A. Griswold ◽  
Nicole Seiberlich ◽  
...  

1999 ◽  
Vol 77 (11) ◽  
pp. 1887-1891
Author(s):  
Richard Buist ◽  
Scott Kroeker ◽  
James Peeling

Creatine kinase (CK) catalyzes the reversible phosphorylation of MgADP by phosphocreatine and thus regulates cellular concentrations of ADP and ATP. The temperature dependence of this reaction has been determined in rat brain in vivo between 30 and 40°C using 31P NMR saturation transfer measurements. The pseudo-first-order rate constant for the forward CK reaction, kf, varies little with temperature over this range, with an apparent activation energy Ea = 14.2 ± 4.9 kJ/mol. This is considerably lower than the values of Ea for isolated CK enzymes. However, when changes in [MgADP] and [H+] with temperature are considered, a substrate concentration-independent value of Ea = 65.3 ± 9.7 kJ/mol is obtained for the maximum forward reaction velocity Vmax. This agrees well with literature values for the isolated brain-type isoform of CK.Key words: creatine kinase, activation energy, temperature, brain, rat.


2019 ◽  
Vol 292 ◽  
pp. 01063
Author(s):  
Lubomír Macků

An alternative method of determining exothermic reactor model parameters which include first order reaction rate constant is described in this paper. The method is based on known in reactor temperature development and is suitable for processes with changing quality of input substances. This method allows us to evaluate the reaction substances composition change and is also capable of the reaction rate constant (parameters of the Arrhenius equation) determination. Method can be used in exothermic batch or semi- batch reactors running processes based on the first order reaction. An example of such process is given here and the problem is shown on its mathematical model with the help of simulations.


Metabolites ◽  
2021 ◽  
Vol 11 (3) ◽  
pp. 176
Author(s):  
Justine Deborne ◽  
Noël Pinaud ◽  
Yannick Crémillieux

The aim of this study was to evaluate the potential of a miniaturized implantable nuclear magnetic resonance (NMR) coil to acquire in vivo proton NMR spectra in sub-microliter regions of interest and to obtain metabolic information using magnetic resonance spectroscopy (MRS) in these small volumes. For this purpose, the NMR microcoils were implanted in the right cortex of healthy rats and in C6 glioma-bearing rats. The dimensions of the microcoil were 450 micrometers wide and 3 mm long. The MRS acquisitions were performed at 7 Tesla using volume coil for RF excitation and microcoil for signal reception. The detection volume of the microcoil was measured equal to 450 nL. A gain in sensitivity equal to 76 was found in favor of implanted microcoil as compared to external surface coil. Nine resonances from metabolites were assigned in the spectra acquired in healthy rats (n = 5) and in glioma-bearing rat (n = 1). The differences in relative amplitude of choline, lactate and creatine resonances observed in glioma-bearing animal were in agreement with published findings on this tumor model. In conclusion, the designed implantable microcoil is suitable for in vivo MRS and can be used for probing the metabolism in localized and very small regions of interest in a tumor.


2011 ◽  
Vol 312-315 ◽  
pp. 364-369 ◽  
Author(s):  
Seyed Amir Bahrani ◽  
Catherine Loisel ◽  
Jean Yves Monteau ◽  
Sid Ahmed Rezzoug ◽  
Zoulikha Maache-Rezzoug

Two hydrothermal treatment processes (DV-HMT and DIC treatment) were investigated on standard maize starch for three processing temperatures; 100, 110 and 120°C. The gravimetric change of starch powder during the treatment was analyzed by a simultaneous water diffusion and starch reaction model. The effective diffusivity coefficient (Deff) and reaction rate constant (k) were estimated by minimizing the error between experimental and analytical results. The values of Deff and k clearly increased with temperature. The degree of starch melting was evaluated for the two treatments using the first-order reaction model as a function of processing time. The results suggest that the absorption process is controlled by water–starch reactivity that induces melting phenomenon of starch crystallites, which progresses when temperature increases. The two hydrothermal treatments considerably differ: DIC being more prone to water absorption as demonstrated by the values of Deff and k.


2009 ◽  
Vol 29 (4) ◽  
pp. 661-669 ◽  
Author(s):  
Jehoon Yang ◽  
Su Xu ◽  
Jun Shen

In vivo13C magnetic resonance spectroscopy has been applied to studying brain metabolic processes by measuring 13C label incorporation into cytosolic pools such as glutamate and aspartate. However, the rate of exchange between mitochondrial α-ketoglutarate/oxaloacetate and cytosolic glutamate/aspartate ( Vx) extracted from metabolic modeling has been controversial. Because brain fumarase is exclusively located in the mitochondria, and mitochondrial fumarate is connected to cytosolic aspartate through a chain of fast exchange reactions, it is possible to directly measure Vx from the four-carbon side of the tricarboxylic acid cycle by magnetization transfer. In isoflurane-anesthetized adult rat brain, a relayed 13C magnetization transfer effect on cytosolic aspartate C2 at 53.2ppm was detected after extensive signal averaging with fumarate C2 at 136.1ppm irradiated using selective radiofrequency pulses. Quantitative analysis using Bloch–McConnell equations and a four-site exchange model found that VxE13–19 µmol per g per min (≫ VTCA, the tricarboxylic acid cycle rate) when the longitudinal relaxation time of malate C2 was assumed to be within ±33% of that of aspartate C2. If VxE VTCA, the isotopic exchange between mitochondria and cytosol would be too slow on the time scale of 13C longitudinal relaxation to cause a detectable magnetization transfer effect.


2000 ◽  
Vol 65 (12) ◽  
pp. 857-866
Author(s):  
Mladjen Micevic ◽  
Slobodan Petrovic

The alcoholysis of 1,2,2-trimethylpropyl-methylfluorophosphonate (soman) was examined with a series of alkoxides and in corresponding alcohols: methanol, ethanol, 1-propanol, 2-propanol, 2-methoxyethanol and 2-ethoxyethanol. Soman reacts with the used alkoxides in a second order reaction, first order in each reactant. The kinetics of the reaction between 1,2,2-trimethylpropyl-methylfluorophosphonate and ethanol in the presence of diethylenetriamine was also examined. A third order reaction rate constant was calculated, first order in each reactant. The activation energy, frequency factor and activation entropy were determined on the basis of the kinetic data.


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