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JBC, Vol. 253, Issue 12, 4305-4309, Jun, 1978
J. T. Whitmer, J. A. Idell-Wenger, M. J. Rovetto and J. R. Neely
The effects of whole heart ischemia on fatty acid metabolism were studied
in the isolated, perfused rat heart. A reduction in coronary flow and
oxygen consumption resulted in lower rates of palmitate uptake and
oxidation to CO2. This decrease in metabolic rate was associated with
increased tissue levels of long chain acyl coenzyme A and long chain
acylcarnitine. Cellular levels of acetyl-CoA, acetylcarnitine, free CoA,
and free carnitine decreased. These changes in CoA and its acyl derivatives
indicate that beta oxidation became the limiting step in fatty acid
metabolism. The rate of beta oxidation was probably limited by high levels
of NADH and FADH2 secondary to a reduced supply of oxygen. Tissue levels of
neutral lipids showed a slight increase durning ischemia, but incorporation
of [U-14C]palmitate into lipid was not altered significantly. Although both
substrates for lipid synthesis were present in higher concentrations during
ischemia, compartmentalization of long chain acyl-CoA in the mitochondrial
matrix and alpha-glycerol phosphate in the cytosol may have accounted for
the relatively low rate of lipid synthesis.
Control of fatty acid metabolism in ischemic and hypoxic hearts
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