Bezafibrate is used to lower serum lipid levels in humans. Fibrate der
ivatives induce an enzyme participating in the beta-oxidation by perox
isomes. We gave ethanol (2 g/kg) orally to bezafibrate-treated (300 mg
/kg) male rats of the Wistar strain. Blood ethanol levels were remarka
bly lower and ethanol elimination stood at 432.6 mg/kg/hr (control, 33
6.6 mg/kg/hr) in the bezafibrate group (p < 0.01). Blood acetate level
s were conversely higher in the bezafibrate group. The fatty acid beta
-oxidation activity of liver peroxisome in bezafibrate-treated, clofib
rate-treated, or gamma-linolenic acid-treated rats for 4 days was assa
yed. The activity was 5.8-fold higher in rats given bezafibrate, 5.4-f
old in the clofibrate (p < 0.01), and 2.0-fold in the gamma-linolenic
acid (p < 0.05). Alcohol dehydrogenase and aldehyde dehydrogenase acti
vity of cytosol in the liver was not induced by the hypolipidemic drug
s, but aldehyde dehydrogenase activity in the liver homogenate was ind
uced. From foregoing results, bezafibrate induced in the organism beta
-oxidation by peroxisomes and increased H2O2 production, which led to
augmented ethanol metabolism by catalase.