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Inhibitors of MAO-A and MAO-B in Psychiatry and Neurology

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Journal Front Pharmacol
Date 2016 Nov 3
PMID 27803666
Citations 139
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Abstract

Inhibitors of MAO-A and MAO-B are in clinical use for the treatment of psychiatric and neurological disorders respectively. Elucidation of the molecular structure of the active sites of the enzymes has enabled a precise determination of the way in which substrates and inhibitor molecules are metabolized, or inhibit metabolism of substrates, respectively. Despite the knowledge of the strong antidepressant efficacy of irreversible MAO inhibitors, their clinical use has been limited by their side effect of potentiation of the cardiovascular effects of dietary amines ("cheese effect"). A number of reversible MAO-A inhibitors which are devoid of cheese effect have been described in the literature, but only one, moclobemide, is currently in clinical use. The irreversible inhibitors of MAO-B, selegiline and rasagiline, are used clinically in treatment of Parkinson's disease, and a recently introduced reversible MAO-B inhibitor, safinamide, has also been found efficacious. Modification of the pharmacokinetic characteristics of selegiline by transdermal administration has led to the development of a new drug form for treatment of depression. The clinical potential of MAO inhibitors together with detailed knowledge of the enzyme's binding site structure should lead to future developments with these drugs.

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References
1.
Coyle J, Snyder S . Antiparkinsonian drugs: inhibition of dopamine uptake in the corpus striatum as a possible mechanism of action. Science. 1969; 166(3907):899-901. DOI: 10.1126/science.166.3907.899. View

2.
Reichmann H, Sommer U, Fuchs G, Hefter H, Mark G, Muller T . Workshop IV: drug treatment guidelines for the long-term management of Parkinson's disease. J Neurol. 2001; 247 Suppl 4:IV/40-1. DOI: 10.1007/pl00007776. View

3.
Denney R, Denney C . An update on the identity crisis of monoamine oxidase: new and old evidence for the independence of MAO A and B. Pharmacol Ther. 1985; 30(3):227-58. DOI: 10.1016/0163-7258(85)90050-6. View

4.
Baker G, Wong J, Yeung J, Coutts R . Effects of the antidepressant phenelzine on brain levels of gamma-aminobutyric acid (GABA). J Affect Disord. 1991; 21(3):207-11. DOI: 10.1016/0165-0327(91)90041-p. View

5.
Palhagen S, Heinonen E, Hagglund J, Kaugesaar T, Maki-Ikola O, Palm R . Selegiline slows the progression of the symptoms of Parkinson disease. Neurology. 2006; 66(8):1200-6. DOI: 10.1212/01.wnl.0000204007.46190.54. View