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Vol. 289, Issue 3, 1648-1653, June 1999
Departments of Pharmacology (M.R.B., H.B.-B., M.R.J.) and
Pediatrics (R.E.P., A.G.F.), School of Medicine, University of
Washington, Seattle, Washington
Cytochrome P-450 2E1 (CYP2E1) is a readily inducible hemoprotein that
catalyzes the oxidation of endogenous compounds and many low molecular
weight xenobiotics. As the major component of the microsomal ethanol
oxidizing system, it contributes significantly to ethanol metabolism
and the formation of the highly reactive metabolite acetaldehyde. The
leaky property of this enzyme results in the generation of reactive
oxygen species that can induce oxidative stress and cytotoxic
conditions deleterious to development. To further investigate the
proposed role of CYP2E1 in the etiology of alcohol teratogenesis, the
current study focused on the quantification of CYP2E1 in prenatal human
brain, a tissue that is highly vulnerable to the damaging effects of
ethanol throughout gestation. In microsomal samples prepared from pools
of brain tissues, immunoreactive protein was detected by Western blot
analysis using enhanced chemiluminescence, whereas functional protein
was estimated with an enzymatic assay using
p-nitrophenol and an electrochemical detection system.
CYP2E1 transcript was consistently detected in RNA samples prepared
from individual brain tissues using the ribonuclease protection assay. Quantitative data were collected by scanning densitometry and phosphorimaging technology. There was a dramatic increase in human brain CYP2E1 content around gestational day 50 and a fairly constant level was maintained throughout the early fetal period, until at least
day 113. The relatively low levels of the P-450 isoform present in
conceptal brain may be sufficient to generate reactive intermediates
that elicit neuroembryotoxicity following maternal alcohol consumption.
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