By Michael A. Conway (Author), Joseph F. Clark (Author)
ISBN-10: 0080530087
ISBN-13: 9780080530086
ISBN-10: 0121863409
ISBN-13: 9780121863401
Creatine and Creatine Phosphate: medical and medical views is an updated precis of either the clinical and clinical points of creatine and creatine phosphate metabolism and therapy.It covers intimately the fundamental biochemistry, bioenergetics and biophysics of those brokers with specific emphasis on their position at the cardiovascular and muscle structures. glossy in vivo myocardial and skeletal muscle measurements are defined, and the significance of the molecules in cardiovascular drugs, game technology and cardiac surgical procedure are highlighted.This publication is designed for these drawn to the fundamental clinical heritage to creatine and creatine phosphate, and in addition for physicians treating or learning middle and vascular sickness. The e-book can also be important for activities scientists who desire to gather a complete wisdom of the molecule that's at present being promoted for functionality and workout programmes.
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Additional info for Creatine and Creatine Phosphate: Scientific and Clinical Perspectives
Example text
Indeed, Clark et al. (1994) found that mitochondrial CK cannot phosphorylate fl-GPA under all experimental conditions studied. 3. Acute fl-GPA administration Chronic administration of/3-GPA appears to create a number of technical problems, including conflicting results from different groups, and possible adaptive and pathological responses that may or may not be directly related to the depletion of Cr and PCr. Comparisons between studies are also complicated as there are differences in both the diet and the age of the animals under investigation.
1992, 1993). 8/zmol/g wet weight, respectively). This normal [creatine] in muscle cannot, therefore, account for the decreased PCr levels. Since there is extensive muscle fibre regeneration in m d x muscle (unlike the human EXPERIMENTALOBSERVATIONSOF PCr AND Cr METABOLISM 41 D M D condition), the decreased PCr level cannot simply be explained by a decreased muscle bulk in muscular dystrophy. These findings raise the question as to what is the cause of the decreased PCr and what effect it has on pathogenesis?
21,202-207. , Wallimann, T. and Carafoli, E. (1990). ATP binding site of mitochondrial creatine kinase: affinity labeling of Asp-335 with CIRATE F E B S Lett. 273, 139-143. I. A. (1988). The cardiac contractile failure induced by chronic creatine and phosphocreatine deficiency. J. Mol. Cell. Cardiol. 20, 465-479. S. V. (1991). Discrete subcellular localization of a cytoplasmic and a mitochondrial isozyme of creatine kinase in intestinal epithelial cells. Cell Motil. Cytoskeleton 19, 169-179. K.
Creatine and Creatine Phosphate: Scientific and Clinical Perspectives by Michael A. Conway (Author), Joseph F. Clark (Author)
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