Key result
Lipid peroxidation preferentially inhibits cardiac Na+,K+-ATPase over microsomal reductase, causing ~90% inhibition.
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Sarcolemmal and microsomal membranes prepared from adult canine cardiac myocytes (sarcolemmal Na+, K+-ATPase = 71.8 mumol/mg per hr and microsomal rotenone-insensitive NADH cytochrome c reductase = 114 mumol/mg per hr) were each preincubated at 37 degrees C in the presence of a free radical generating system consisting of dihydroxyfumarate and Fe -ADP; loss of the Na+, K+-ATPase and reductase activities, as well as the associated increases in lipid peroxidation, measured by malondialdehyde formation, were temporally correlated in both systems. The ATPase was inhibited 70% when the malondialdehyde was 71 nmol/mg protein at 20 minutes and 90% when malondialdehyde was 138 nmol/mg protein at 90 minutes. Inhibition of reductase activity occurred more gradually, displaying a 27% loss of activity when malondialdehyde reached 34 nmol/mg protein at 20 minutes and 60% with a malondialdehyde value of 67 nmol/mg protein at 90 minutes. The greater susceptibility of the sarcolemma to free radical-induced membrane damage may be due to the higher content of unsaturated fatty acids in this membrane, compared to microsomes.
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Krämer et al. (1984) studied Free radical-induced cardiac membrane lipid peroxidation. Free radical generating system (dihydroxyfumarate and Fe-ADP) on sarcolemmal membranes vs. Microsomal membranes under the same free radical generating system was evaluated on Percentage inhibition of enzyme activity (sarcolemmal Na+, K+-ATPase vs microsomal NADH cytochrome c reductase) at 90 minutes. Free radical-induced lipid peroxidation inhibited canine cardiac sarcolemmal Na+,K+-ATPase more rapidly than microsomal reductase (70% vs 27% at 20 min; 90% vs 60% at 90 min).
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