Document Detail


The role of phosphorylcreatine and creatine in the regulation of mitochondrial respiration in human skeletal muscle.
MedLine Citation:
PMID:  11744769     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
1. The role of phosphorylcreatine (PCr) and creatine (Cr) in the regulation of mitochondrial respiration was investigated in permeabilised fibre bundles prepared from human vastus lateralis muscle. 2. Fibre respiration was measured in the absence of ADP (V(0)) and after sequential additions of submaximal ADP (0.1 mM ADP, V(submax)), PCr (or Cr) and saturating [ADP] (V(max)). 3. V(submax) increased by 55 % after addition of saturating creatine (P < 0.01; n = 8) and half the maximal effect was obtained at 5 mM [Cr]. In contrast, V(submax) decreased by 54 % after addition of saturating phosphorylcreatine (P < 0.01; n = 8) and half the maximal effect was obtained at 1 mM [PCr]. V(max) was not affected by Cr or PCr. 4. V(submax) was similar when PCr and Cr were added simultaneously at concentrations similar to those in muscle at rest (PCr/Cr = 2) and at low-intensity exercise (PCr/Cr = 0.5). At conditions mimicking high-intensity exercise (PCr/Cr = 0.1), V(submax) increased to 60 % of V(max) (P < 0.01 vs. rest and low-intensity exercise). 5. Eight of the subjects participated in a 16 day Cr supplementation programme. Following Cr supplementation, V(0) decreased by 17 % (P < 0.01 vs. prior to Cr supplementation), whereas ADP-stimulated respiration (with and without Cr or PCr) was unchanged. 6. For the first time evidence is given that PCr is an important regulator of mitochondrial ADP-stimulated respiration. Phosphorylcreatine decreases the sensitivity of mitochondrial respiration to ADP whereas Cr has the opposite effect. During transition from rest to high-intensity exercise, decreases in the PCr/Cr ratio will effectively increase the sensitivity of mitochondrial respiration to ADP. The decrease in V(0) after Cr supplementation indicates that intrinsic changes in membrane proton conductance occur.
Authors:
B Walsh; M Tonkonogi; K Söderlund; E Hultman; V Saks; K Sahlin
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Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't    
Journal Detail:
Title:  The Journal of physiology     Volume:  537     ISSN:  0022-3751     ISO Abbreviation:  J. Physiol. (Lond.)     Publication Date:  2001 Dec 
Date Detail:
Created Date:  2001-12-17     Completed Date:  2002-03-19     Revised Date:  2013-06-09    
Medline Journal Info:
Nlm Unique ID:  0266262     Medline TA:  J Physiol     Country:  England    
Other Details:
Languages:  eng     Pagination:  971-8     Citation Subset:  IM    
Affiliation:
Department of Physiology and Pharmacology, Karolinska Institute, Stockholm, Sweden.
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MeSH Terms
Descriptor/Qualifier:
Adenosine Diphosphate / pharmacology
Adult
Creatine / pharmacology,  physiology*
Exercise / physiology
Humans
Male
Mitochondria, Muscle / metabolism*
Muscle, Skeletal / metabolism*
Oxygen Consumption / drug effects,  physiology*
Phosphocreatine / pharmacology,  physiology*
Chemical
Reg. No./Substance:
57-00-1/Creatine; 58-64-0/Adenosine Diphosphate; 67-07-2/Phosphocreatine
Comments/Corrections
Comment In:
J Physiol. 2001 Dec 15;537(Pt 3):657   [PMID:  11744744 ]

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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