Effects of short-term ozone exposure on lung mitochondrial oxidative and energy metabolism

MG Mustafa, CE Cross - Archives of Biochemistry and Biophysics, 1974 - Elsevier
MG Mustafa, CE Cross
Archives of Biochemistry and Biophysics, 1974Elsevier
Ozone effects on lung mitochondrial oxidative metabolism were examined after short-term
exposure of rats and monkeys to O 3. Exposure of animals to 2 ppm O 3 for 8 hr or to 4 ppm
O 3 for 4 hr caused a 15–27%(P< 0.05) depression of lung mitochondrial O 2 consumption,
using 2-oxoglutarate, succinate, and glycerol-1-phosphate. but not ascorbate plus Wurster's
blue as substrates. Under these exposure conditions (4 ppm 4 hr) the ADP: O ratios dropped
25–36%(P< 0.05) and the respiratory control indices decreased 27–33%(P< 0.02) for …
Abstract
Ozone effects on lung mitochondrial oxidative metabolism were examined after short-term exposure of rats and monkeys to O3. Exposure of animals to 2 ppm O3 for 8 hr or to 4 ppm O3 for 4 hr caused a 15–27% (P < 0.05) depression of lung mitochondrial O2 consumption, using 2-oxoglutarate, succinate, and glycerol-1-phosphate. but not ascorbate plus Wurster's blue as substrates. Under these exposure conditions (4 ppm 4 hr) the ADP:O ratios dropped 25–36% (P < 0.05) and the respiratory control indices decreased 27–33% (P < 0.02) for oxidation of all substrates examined. Lung mitochondria from control animals were relatively impermeable to added NADH, but those from O3-exposed animals showed an increased permeability as judged from NADH oxidation at a rate 3-fold higher than the control. Likewise, added cytochrome c caused a 22% (P < 0.01) stimulation of succinate oxidation in exposed lung mitochondria as against 5% (nonsignificant) in controls. Ozone exposure also caused a 20% (P < 0.01) oxidation of thiol groups in lung mitochondria, but no lipid peroxidation products were detectable in O3-exposed lung tissue. The depression of substrate utilization, coupled phosphorylation and respiratory control observed in lung mitochondria of O3-exposed animals might be related to alteration of membrane permeability, and inhibition of respiratory enzymes (dehydrogenases) due to oxidation of functional thiol groups.
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