Document Detail


Comparison of in vivo postexercise phosphocreatine recovery and resting ATP synthesis flux for the assessment of skeletal muscle mitochondrial function.
MedLine Citation:
PMID:  20668212     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
(31)P magnetic resonance spectroscopy (MRS) has been used to assess skeletal muscle mitochondrial function in vivo by measuring 1) phosphocreatine (PCr) recovery after exercise or 2) resting ATP synthesis flux with saturation transfer (ST). In this study, we compared both parameters in a rat model of mitochondrial dysfunction with the aim of establishing the most appropriate method for the assessment of in vivo muscle mitochondrial function. Mitochondrial dysfunction was induced in adult Wistar rats by daily subcutaneous injections with the complex I inhibitor diphenyleneiodonium (DPI) for 2 wk. In vivo (31)P MRS measurements were supplemented by in vitro measurements of oxygen consumption in isolated mitochondria. Two weeks of DPI treatment induced mitochondrial dysfunction, as evidenced by a 20% lower maximal ADP-stimulated oxygen consumption rate in isolated mitochondria from DPI-treated rats oxidizing pyruvate plus malate. This was paralleled by a 46% decrease in in vivo oxidative capacity, determined from postexercise PCr recovery. Interestingly, no significant difference in resting, ST-based ATP synthesis flux was observed between DPI-treated rats and controls. These results show that PCr recovery after exercise has a more direct relationship with skeletal muscle mitochondrial function than the ATP synthesis flux measured with (31)P ST MRS in the resting state.
Authors:
N M A van den Broek; J Ciapaite; K Nicolay; J J Prompers
Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't     Date:  2010-07-28
Journal Detail:
Title:  American journal of physiology. Cell physiology     Volume:  299     ISSN:  1522-1563     ISO Abbreviation:  Am. J. Physiol., Cell Physiol.     Publication Date:  2010 Nov 
Date Detail:
Created Date:  2010-10-28     Completed Date:  2010-11-22     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  100901225     Medline TA:  Am J Physiol Cell Physiol     Country:  United States    
Other Details:
Languages:  eng     Pagination:  C1136-43     Citation Subset:  IM    
Affiliation:
Biomedical NMR, Department of Biomedical Engineering, Eindhoven University of Technology, Eindhoven, The Netherlands.
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Descriptor/Qualifier:
Adenosine Diphosphate / metabolism
Adenosine Triphosphate / biosynthesis*
Animals
Enzyme Inhibitors / pharmacology
Hydrogen-Ion Concentration
Magnetic Resonance Spectroscopy
Male
Mitochondria, Muscle / drug effects,  metabolism*
Muscle, Skeletal / metabolism*,  ultrastructure
Onium Compounds / pharmacology
Oxidative Phosphorylation
Oxygen Consumption
Phosphocreatine / metabolism*
Physical Conditioning, Animal / physiology*
Rats
Rats, Wistar
Chemical
Reg. No./Substance:
0/Enzyme Inhibitors; 0/Onium Compounds; 244-54-2/diphenyleneiodonium; 56-65-5/Adenosine Triphosphate; 58-64-0/Adenosine Diphosphate; 67-07-2/Phosphocreatine

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


Previous Document:  Adrenergic receptor activation involves ATP release and feedback through purinergic receptors.
Next Document:  Somatic ATP release from guinea pig sympathetic neurons does not require calcium-induced calcium rel...