Abstract

1.1. Effects of ethanol on mitochondrial oxidations in vitro have been studied.2.2. Ethanol in relatively low concentrations was found to stimulate the O2 uptake of rat-liver mitochondria with β-hydroxybutyrate as the substrate. With pyruvate, α-ketoglutarate and succinate as substrate ethanol depressed the O2 uptake.3.3. With β-hydroxybutyrate the O2 uptake increased with increasing ethanol concentration to reach a maximum of 130–135% of the control value at 0.5–0.6 M ethanol. The increased O2 could be accounted for by a stoichiometric increase in the acetoacetate formation.4.4. Sonic disruption of the mitochondria prior to incubation nearly abolished the stimulating effect of ethanol on the O2 consumption.5.5. The activity of β-hydroxybutyrate (D-3-hydroxybutyrate: NAD oxidoreductase, EC 1.1.1.30) was not affected by ethanol in concentrations which stimulated the mitochondrial O2 uptake with β-hydroxybutyrate.6.6. The P/O ratio was not lowered by ethanol concentrations which increased the β-hydroxybutyrate oxidation.7.7. It is suggested that ethanol increases the oxidation of the β-hydroxybutyrate, by facilitating its transport into the mitochondria.

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