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Publication Detail

Title: Expression of CYP2E1 during embryogenesis and fetogenesis in human cephalic tissues: implications for the fetal alcohol syndrome.

Authors: Boutelet-Bochan, H; Huang, Y; Juchau, M R

Published In Biochem Biophys Res Commun, (1997 Sep 18)

Abstract: Reverse transcription and the polymerase chain reaction (RT-PCR) with oligonucleotide primers designed to target cDNA nucleotides 1241-1357 corresponding to exons 8 (3' end) and 9 (5' end) in human genomic CYP2E1 detected consistently strong signals in 9 of 10 prenatal human brains. Cephalic tissues analyzed were between 54 and 78 days of gestation. RT-PCR signals for expression of CYP2E1 in corresponding human hepatic or adrenal tissues were weaker or, with only 2 exceptions, undetectable. Attempts to approximate levels of P4502E1 mRNA with Northern blots and RNase protection assays indicated that levels in human prenatal whole brain tissues tended to increase as a function of gestational age but, at the early stages investigated, were far lower than the constitutive levels in hepatic tissues of adult humans or male rats. Localized, P4502E1-dependent cephalic bioactivation of ethanol, with associated generation of several reactive chemical species, could contribute significantly to the etiology of neuroembryotoxic effects of prenatal ethanol exposure.

PubMed ID: 9299528 Exiting the NIEHS site

MeSH Terms: Adult; Animals; Brain/embryology; Brain/enzymology*; Cytochrome P-450 CYP2E1/biosynthesis*; Fetal Alcohol Spectrum Disorders*; Gene Expression Regulation, Developmental; Gene Expression Regulation, Enzymologic; Humans; Male; RNA, Messenger/analysis; Rats

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