Literature DB >> 21971008

Selective inhibitors of monoamine oxidase type B and the "cheese effect".

John P M Finberg1, Ken Gillman.   

Abstract

Potentiation of the cardiovascular and other effects of dietary tyramine by monoamine oxidase (MAO) inhibitors (cheese effect) has been a major limitation to clinical use of these drugs. The discovery that MAO exists in two distinct isoforms, MAO-A and MAO-B, together with the development of selective inhibitors of each isoform, enabled the understanding that selective inhibition of MAO-A, or inhibition of both isoforms, will cause cheese effect, but selective inhibition of MAO-B can be elicited without dangerous pressor reaction. This development has permitted the introduction of selective MAO-B inhibitors to clinical medicine for treatment of Parkinson's disease. This review describes the basic mechanisms involved in cheese effect, as well as providing information on tyramine levels in a variety of foodstuff, and surveys clinical information from tyramine pressor testing with the selective MAO-B inhibitors, selegiline and rasagiline.
Copyright © 2011 Elsevier Inc. All rights reserved.

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Year:  2011        PMID: 21971008     DOI: 10.1016/B978-0-12-386467-3.00009-1

Source DB:  PubMed          Journal:  Int Rev Neurobiol        ISSN: 0074-7742            Impact factor:   3.230


  24 in total

Review 1.  Inhibitors of MAO-B and COMT: their effects on brain dopamine levels and uses in Parkinson's disease.

Authors:  John P M Finberg
Journal:  J Neural Transm (Vienna)       Date:  2018-11-01       Impact factor: 3.575

2.  Cerebral MAO Activity Is Not Altered by a Novel Herbal Antidepressant Treatment.

Authors:  Ravid Doron; Ziv Versano; Or Burstein; Motty Franko; Alon Shamir; Roni Toledano; Assaf Handelsman; Moshe Rehavi
Journal:  J Mol Neurosci       Date:  2019-07-09       Impact factor: 3.444

3.  Non-Oral Drug Delivery in Parkinson's Disease: Current Applications and Future.

Authors:  Meliha Güneş; Sinem Yaprak Karavana
Journal:  Turk J Pharm Sci       Date:  2022-06-27

4.  Mechanisms of the antilipolytic response of human adipocytes to tyramine, a trace amine present in food.

Authors:  Christian Carpéné; Jean Galitzky; Chloé Belles; Alexia Zakaroff-Girard
Journal:  J Physiol Biochem       Date:  2018-07-23       Impact factor: 4.158

5.  Body fat reduction without cardiovascular changes in mice after oral treatment with the MAO inhibitor phenelzine.

Authors:  Christian Carpéné; Josep Mercader; Sophie Le Gonidec; Stéphane Schaak; Jeanne Mialet-Perez; Alexia Zakaroff-Girard; Jean Galitzky
Journal:  Br J Pharmacol       Date:  2018-05-06       Impact factor: 8.739

6.  High intake of dietary tyramine does not deteriorate glucose handling and does not cause adverse cardiovascular effects in mice.

Authors:  Christian Carpéné; Stéphane Schaak; Céline Guilbeau-Frugier; Josep Mercader; Jeanne Mialet-Perez
Journal:  J Physiol Biochem       Date:  2015-12-03       Impact factor: 4.158

Review 7.  Current place of monoamine oxidase inhibitors in the treatment of depression.

Authors:  Kenneth I Shulman; Nathan Herrmann; Scott E Walker
Journal:  CNS Drugs       Date:  2013-10       Impact factor: 5.749

8.  Parkinson's Disease and Its Management: Part 3: Nondopaminergic and Nonpharmacological Treatment Options.

Authors:  George DeMaagd; Ashok Philip
Journal:  P T       Date:  2015-10

Review 9.  Methylene blue and its analogues as antidepressant compounds.

Authors:  Anzelle Delport; Brian H Harvey; Anél Petzer; Jacobus P Petzer
Journal:  Metab Brain Dis       Date:  2017-07-31       Impact factor: 3.584

10.  High doses of tyramine stimulate glucose transport in human fat cells.

Authors:  Christian Carpéné; Francisco Les; Josep Mercader-Barceló; Nathalie Boulet; Anaïs Briot; Jean-Louis Grolleau
Journal:  J Physiol Biochem       Date:  2022-01-23       Impact factor: 4.158

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