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Vol. 298, Issue 2, 737-743, August 2001
Institut National de la Santé et de la Recherche
Médicale Unité 481 and Centre de Recherches de
l'Association Claude Bernard sur les Hépatites Virales,
Hôpital Beaujon, Clichy, France
Ethanol metabolism causes oxidative stress and lipid peroxidation not
only in liver but also in extra-hepatic tissues. Ethanol administration
has been shown to cause oxidative degradation and depletion of hepatic
mitochondrial DNA (mtDNA) in rodents, but its in vivo effects on the
mtDNA of extra-hepatic tissues have not been assessed. We studied the
effects of an acute intragastric ethanol administration (5 g/kg) on
brain, heart, skeletal muscle, and liver mtDNA in mice. Ethanol
administration caused mtDNA depletion and replacement of its
supercoiled form by linearized forms in all tissues examined. Maximal
mtDNA depletion was about similar (ca. 50%) in all organs studied. It
occurred 2 h after ethanol administration in heart, skeletal
muscle, and liver but after 10 h in brain. This mtDNA depletion
was followed by increased mtDNA synthesis. A secondary, transient
increase in mtDNA levels occurred 24 h after ethanol
administration in all organs. In hepatic or extra-hepatic tissues,
mtDNA degradation and depletion were prevented by 4-methylpyrazole, an
inhibitor of ethanol metabolism, and attenuated by vitamin E,
melatonin, or coenzyme Q, three antioxidants. In conclusion, our study
shows for the first time that ethanol metabolism also causes oxidative
degradation of the mitochondrial genome in brain, heart, and skeletal
muscles. These effects could contribute to the development of
(cardio)myopathy and brain injury in some alcoholic patients.
Antioxidants prevent these effects in mice and could be useful in
persevering drinkers.
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