| 2007 JASN IMPACT FACTOR 7.111 | HOME AUTHOR INFO EDITORIAL BOARD SUBSCRIBE FEEDBACK ALERTS HELP | |||
| CURRENT ISSUE | ARCHIVES | JASN Express | ONLINE SUBMISSION | |
Journal of the American Society of Nephrology, Vol 6, 68-74, Copyright © 1995 by American Society of Nephrology
REGULAR ARTICLES |
A Conjard, B Ferrier, M Martin, A Caillette, H Carrier and G Baverel
Laboratoire de Physiopathologie Metabolique et Renale (INSERM C.R.I. 95- 02-01), Faculte de Medecine Alexis Carrel, Lyon, France.
In order to improve knowledge about the mechanisms underlying the alterations of energy metabolism recently observed in the skeletal muscle of patients suffering from chronic renal failure, this study was designed to test (1) whether changes in the activity of key enzymes of energy metabolism occur in the muscle of these patients, and if so (2) whether the different muscle fiber types are equally altered in their metabolic machinery. For this, the maximum activities of 14 enzymes were measured in individual muscle fibers microdissected from biopsies of rectus abdominis muscle obtained from seven normal subjects and seven patients with end-stage renal failure before renal replacement therapy. A large decrease in the activities of beta-hydroxyacyl- coenzyme A dehydrogenase, a key enzyme of the beta-oxidation pathway, of citrate synthase, which initiates the tricarboxylic acid cycle, and of fructose-1,6-bisphosphatase, which contributes to the synthesis of glycogen from lactate, was observed in the three fiber types (slow- twitch oxidative, fast-twitch oxidative-glycolytic, and fast-twitch glycolytic). A smaller reduction of the activities of phosphofructokinase and/or pyruvate kinase, two key enzymes of glycolysis, was also observed in slow-twitch oxidative and/or fast- twitch oxidative-glycolytic fibers. These results demonstrate that the abnormalities of muscle energy metabolism observed in patients with chronic renal failure are due, at least in part, to intrinsic changes in the key enzymes of major energy-providing pathways; they also offer a satisfactory explanation for the defect of oxidative metabolism recently demonstrated in the muscle of these patients.
This article has been cited by other articles:
![]() |
G. R. Adams and N. D. Vaziri Skeletal muscle dysfunction in chronic renal failure: effects of exercise Am J Physiol Renal Physiol, April 1, 2006; 290(4): F753 - F761. [Abstract] [Full Text] [PDF] |
||||
![]() |
C. M. Avesani, S. A. Draibe, M. A. Kamimura, M. A. Dalboni, F. A. B. Colugnati, and L. Cuppari Decreased resting energy expenditure in non-dialysed chronic kidney disease patients Nephrol. Dial. Transplant., December 1, 2004; 19(12): 3091 - 3097. [Abstract] [Full Text] [PDF] |
||||
![]() |
G. J. Kemp, A. V. Crowe, H. K. I. Anijeet, Q. Y. Gong, W. E. Bimson, S. P. Frostick, J. M. Bone, G. M. Bell, and J. N. Roberts Abnormal mitochondrial function and muscle wasting, but normal contractile efficiency, in haemodialysed patients studied non-invasively in vivo Nephrol. Dial. Transplant., June 1, 2004; 19(6): 1520 - 1527. [Abstract] [Full Text] [PDF] |
||||
![]() |
G. K. Sakkas, D. Ball, T. H. Mercer, A. J. Sargeant, K. Tolfrey, and P. F. Naish Atrophy of non-locomotor muscle in patients with end-stage renal failure Nephrol. Dial. Transplant., October 1, 2003; 18(10): 2074 - 2081. [Abstract] [Full Text] [PDF] |
||||
![]() |
C. Haller, J. Zehelein, A. Remppis, M. Muller-Bardorff, and H. A. Katus Cardiac troponin T in patients with end-stage renal disease: absence of expression in truncal skeletal muscle Clin. Chem., May 1, 1998; 44(5): 930 - 938. [Abstract] [Full Text] [PDF] |
||||
|
HOME
CURRENT ISSUE
ARCHIVES
JASN Express
ONLINE SUBMISSION
AUTHOR INFO
EDITORIAL BOARD SUBSCRIBE FEEDBACK ALERTS HELP |
Copyright © 2008 by the American Society of Nephrology. Online ISSN: 1533-3450 Print ISSN: 1046-6673