6533b870fe1ef96bd12cf2e9

RESEARCH PRODUCT

MUSCLE BIOENERGETICS IN OBESE ZUCKER RATS

Marc KleinPaul WalkerJ. StraczekF BarbéPierre KaminskyM. DucClaude Burlet

subject

medicine.medical_specialtyMagnetic Resonance SpectroscopyPhysiologyEndocrinology Diabetes and MetabolismIntracellular pHPHOSPHOCREATINE[INFO.INFO-IM] Computer Science [cs]/Medical ImagingStimulation030204 cardiovascular system & hematologyBiologyPhosphatesPhosphocreatine03 medical and health scienceschemistry.chemical_compoundAdenosine Triphosphate0302 clinical medicineMITOCHONDRIAGENETIC OBESITYPhysiology (medical)Internal medicineMUSCLESmedicine[INFO.INFO-IM]Computer Science [cs]/Medical ImagingAnimalsNUCLEAR MAGNETIC RESONANCEObesityAcidosis2. Zero hungerAnalysis of Variance[ INFO.INFO-IM ] Computer Science [cs]/Medical ImagingADENOSINE 5'-TRIPHOSPHATEADENOSINE 5'-DIPHOSPHATEMetabolismElectric StimulationRatsRats ZuckerAdenosine DiphosphateAdenosine diphosphateEndocrinologychemistryENERGETIC METABOLISMINTRACELLULAR PHFemalemedicine.symptomEnergy MetabolismAdenosine triphosphate030217 neurology & neurosurgeryMuscle ContractionMuscle contraction

description

International audience; Abstract: The purpose of this study was to investigate the energetic metabolism in obese Zucker rats, using phosphorus nuclear magnetic resonance spectroscopy at rest and during a 2-Hz muscle stimulation and subsequent recovery. Animals were anesthetized with ketamine (150 mg/kg ip). Fed obese rats and 2-day-fasted obese rats were compared with their normally fed and 2-day-fasted lean litter mates. No differences were found between the two groups for ATP, total creatine, phosphocreatine (PCr), and intracellular pH. Starvation in lean rats resulted in a significant fall in inorganic phosphate (Pi), increased resting ADP level, and decreased PCr and ADP recovery after stimulation. The obese rats exhibited a decreased PCr/Pi and increased ADP at rest and a decreased PCr resynthesis and ADP metabolization rate after stimulation. Muscle stimulation in fasted obese rats induced higher PCr depletion and more pronounced acidosis. These results suggest an in vivo mitochondrial metabolism dysfunction in fasted lean as well as in fed and fasted obese rats.

https://hal.archives-ouvertes.fr/hal-00790168