Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2013:67:235-47.
doi: 10.1007/978-94-007-5881-0_8.

The role of CYP2E1 in alcohol metabolism and sensitivity in the central nervous system

Affiliations
Review

The role of CYP2E1 in alcohol metabolism and sensitivity in the central nervous system

Claire Heit et al. Subcell Biochem. 2013.

Abstract

Ethanol consumption has effects on the central nervous system (CNS), manifesting as motor incoordination, sleep induction (hypnosis), anxiety, amnesia, and the reinforcement or aversion of alcohol consumption. Acetaldehyde (the direct metabolite of ethanol oxidation) contributes to many aspects of the behavioral effects of ethanol. Given acetaldehyde cannot pass through the blood brain barrier, its concentration in the CNS is primarily determined by local production from ethanol. Catalase and cytochrome P450 2E1 (CYP2E1) represent the major enzymes in the CNS that catalyze ethanol oxidation. CYP2E1 is expressed abundantly within the microsomes of certain brain cells and is localized to particular brain regions. This chapter focuses on the discussion of CYP2E1 in ethanol metabolism in the CNS, covering topics including how it is regulated, where it is expressed and how it influences sensitivity to ethanol in the brain.

PubMed Disclaimer

Figures

Figure 1
Figure 1. Metabolic pathways of ethanol metabolism in the Central Nervous System (CNS)
Three enzymes are responsible for oxidizing ethanol to acetaldehyde: alcohol dehydrogenase (ADH), catalase and cytochrome P450 2E1 (CYP2E1). Acetaldehyde is further oxidized to acetate by acetaldehyde dehydrogenase (ALDH). Acetaldehyde is responsible for many of the behavioral effects associated with ethanol consumption. The contribution of each enzyme to total ethanol oxidation occurring in the CNS is as follows: catalase, serving as the primary enzyme, accounts for 60%; CYP2E1 is inducible and accounts for 20%; the remaining 20% is unknown but is thought to involve ADH. Isoforms of ADH present in the CNS have a wide range of affinity for ethanol.

References

    1. Abdulla D, Goralski KB, et al. The regulation of cytochrome P450 2E1 during LPS-induced inflammation in the rat. Toxicol Appl Pharmacol. 2006;216(1):1–10. - PubMed
    1. Alfonso-Loeches S, Guerri C. Molecular and behavioral aspects of the actions of alcohol on the adult and developing brain. Crit Rev Clin Lab Sci. 2011;48(1):19–47. - PubMed
    1. Aragon CM, Rogan F, et al. Ethanol metabolism in rat brain homogenates by a catalase-H2O2 system. Biochem Pharmacol. 1992;44(1):93–98. - PubMed
    1. Bansal S, Liu CP, et al. Mitochondria-targeted cytochrome P450 2E1 induces oxidative damage and augments alcohol-mediated oxidative stress. J Biol Chem. 2010;285(32):24609–24619. - PMC - PubMed
    1. Beisswenger TB, Holmquist B, et al. chi-ADH is the sole alcohol dehydrogenase isozyme of mammalian brains: implications and inferences. Proc Natl Acad Sci U S A. 1985;82(24):8369–8373. - PMC - PubMed

MeSH terms