Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1926929 | Archives of Biochemistry and Biophysics | 2007 | 8 Pages |
Anaplerosis from propionate was investigated in rat hearts perfused with 0–2 mM [13C3]propionate and physiological concentrations of glucose, lactate, and pyruvate. The data show that when the concentration of [13C3]propionate was raised from 0 to 2 mM, total anaplerosis increased from 5% to 16% of the turnover of citric acid cycle intermediates. Then, [13C3]propionate abolished anaplerosis from endogenous substrates, glucose, lactate, and pyruvate. Also, while the contents of propionyl-CoA and methylmalonyl-CoA increased with [13C3]propionate concentration, the content of succinyl-CoA decreased, presumably via activation of succinyl-CoA hydrolysis by a decrease in free CoA. Under our conditions, [13C3]propionate was a purely anaplerotic substrate since there was no labeling of mitochondrial acetyl-CoA, reflected by the labeling of the acetyl moiety of citrate.