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Biochem Med Metab Biol ; 35(3): 248-59, 1986 Jun.
Article in English | MEDLINE | ID: mdl-3087394

ABSTRACT

Palmitate oxidation was comparatively assayed in various cell-free and cellular systems by 14CO2 production and by the sum of 14CO2 and 14C-labeled acid-soluble products. The 14CO2 production rate was dependent on incubation time and amount of tissue in contrast to the total oxidation rate. The 14CO2 contribution to the oxidation rate of [1-14C]palmitate varied with homogenates from 1% with rat liver to 28% with rat kidney and amounted to only 2-4% with human muscles. With cellular systems the 14CO2 contribution varied between 20% in human fibroblasts and 70% in rat muscles and myocytes. Addition of cofactors increased the oxidation rate, but decreased the 14CO2 contribution. Various conditions appeared also to influence to a different extent the 14CO2 production and the total oxidation rate with rat tissue homogenates and with rat muscle mitochondria. Incorporation of radioactivity from [1-14C]palmitate into protein was not detectable in cell-free systems and only 2-3% of the sum of 14CO2 and 14C-labeled acid-soluble products in cellular systems. Assay of 14CO2 and 14C-labeled acid-soluble products is a much more accurate and sensitive estimation of fatty acid oxidation than assay of only 14CO2.


Subject(s)
Carbon Dioxide/analysis , Muscles/metabolism , Palmitic Acids/metabolism , Animals , Carbon Radioisotopes , Fasting , Fibroblasts/metabolism , Liver/metabolism , Male , Mitochondria, Muscle/metabolism , Myocardium/metabolism , Organ Specificity , Oxidation-Reduction , Palmitic Acid , Physical Exertion , Radioisotope Dilution Technique , Rats , Rats, Inbred Strains
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