Temporal changes in P-450 2E1 expression with continued ethylbenzene exposure

Biochim Biophys Acta. 1994 Aug 17;1207(2):179-86. doi: 10.1016/0167-4838(94)00070-0.


The goal of this study was to examine the effect of duration of ethylbenzene exposure on cytochrome P-450-dependent activities. Male rats were treated with ethylbenzene by intraperitoneal injection for either 1 or 3 days, and microsomal preparations were examined for changes in the microsomal proteins and activities as well as the expression of specific P-450 isozymes. Two general patterns of induction were evident when different P-450-dependent activities were examined. (i) Cytochrome P-450 2B-dependent activities (e.g., p-nitroanisole demethylation, benzphetamine demethylation, and aromatic toluene hydroxylations) were induced both after 1 and 3 days of ethylbenzene exposure. (ii) Cytochrome P-450 2E1-dependent activities (e.g., N,N-dimethylnitrosamine demethylation and aniline hydroxylation) were induced after treatment with ethylbenzene for one day; however, after 3 days of ethylbenzene treatment these activities returned to control levels. Changes in these activities were consistent with changes in the levels of specific P-450 isozymes as determined by immunoblotting. Cytochrome P-450 2B levels were increased and P-450 2C11 levels were suppressed at both 1 and 3 days of ethylbenzene exposure. A temporal response in P-450 2E1 expression was observed, with P-450 2E1 levels increasing after a single ethylbenzene injection and returning to controls after administration of the hydrocarbon for 3 days. Rats were also subjected to a pair-feeding regimen to determine whether these effects were related to altered dietary status in ethylbenzene-treated rats. Neither P-450-dependent activities nor immunoreactive protein levels were altered in pair-fed rats. These results demonstrate that prolonging the duration of hydrocarbon exposure can produce differential effects on the expression of P-450 2E1, with levels being elevated after acute hydrocarbon administration, but not after more prolonged hydrocarbon exposure.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Aniline Compounds / metabolism
  • Animals
  • Anisoles / metabolism
  • Benzene Derivatives / administration & dosage
  • Benzene Derivatives / pharmacology*
  • Cytochrome P-450 CYP2E1
  • Cytochrome P-450 Enzyme System / metabolism*
  • Dimethylnitrosamine / metabolism
  • Eating / drug effects
  • Hydroxylation
  • Isoenzymes / metabolism
  • Kinetics
  • Male
  • Methylation
  • Microsomes, Liver / drug effects
  • Microsomes, Liver / enzymology*
  • Oxidoreductases, N-Demethylating / metabolism*
  • Rats


  • Aniline Compounds
  • Anisoles
  • Benzene Derivatives
  • Isoenzymes
  • Cytochrome P-450 Enzyme System
  • Cytochrome P-450 CYP2E1
  • Oxidoreductases, N-Demethylating
  • 4-nitroanisole
  • ethylbenzene
  • Dimethylnitrosamine
  • aniline