Neutral endopeptidase and alcohol consumption, experiments in neutral endopeptidase-deficient mice

Wolf Eberhard Siems, Bjoern Maul, Winfried Krause, Craig Gerard, Kurt F. Hauser, Louis B. Hersh, Hanspeter S. Fischer, Gerald Zernig, Alois Saria

Research output: Contribution to journalArticlepeer-review

17 Scopus citations

Abstract

Alcohol consumption was investigated in mice which were rendered deficient in the peptide-degrading enzyme neutral endopeptidase (EC 3.4.24.11) (NEP-/-) by gene targeting and compared to alcohol consumption in corresponding wild type mice (NEP+/+). Mice were offered a free choice to drink tap water or 10% alcohol. The NEP-/- mice consumed significantly more alcohol (~42%) than the NEP+/+ mice, whereas no significant differences were observed in the total fluid consumption. The daily food consumption of alcohol naive NEP-/- animals was elevated (~29%). Furthermore, the activities of peptidases closely related to neutral endopeptidase were analysed ex vivo in several brain regions from NEP-/- and NEP+/+ mice not treated with alcohol. There was no obvious compensation for the total loss of neutral endopeptidase by the functionally related peptidases angiotensin-converting enzyme and aminopeptidase N. In vitro, the degradation of exogenously applied [Leu5]enkephalin was not reduced in membrane preparations of those brain regions assayed in NEP-/- mice. A small reduction in [Leu5]enkephalin degradation was detected in striatal membrane preparations of NEP-/- mice, if aminopeptidase N was additionally blocked by bestatin or amastatin. Copyright (C) 2000 Elsevier Science B.V.

Original languageEnglish
Pages (from-to)327-334
Number of pages8
JournalEuropean Journal of Pharmacology
Volume397
Issue number2-3
DOIs
StatePublished - Jun 2 2000

Bibliographical note

Funding Information:
The authors are grateful for the excellent technical assistance of R. Lange and M. Schlender. This work was supported in part by NIH grants DA02243 to LBH and DA06204 to KFH.

Funding

The authors are grateful for the excellent technical assistance of R. Lange and M. Schlender. This work was supported in part by NIH grants DA02243 to LBH and DA06204 to KFH.

FundersFunder number
National Institutes of Health (NIH)DA06204
National Institute on Drug AbuseR01DA002243

    Keywords

    • Alcohol consumption
    • Angiotensin-converting enzyme
    • Enkephalin
    • Enkephalin-degrading peptidases
    • Enkephalinase
    • Knockout mouse
    • Neutral endopeptidase
    • Opioid

    ASJC Scopus subject areas

    • Pharmacology

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