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Dopamine is a monoamine oxidase B substrate in man
DURING the past decade, the central neurotransmitter, dopamine (DA), has been much studied for it is known to be involved in certain human disease states, Parkinsonism 1 preeminently, and rather more inferentially, schizophrenia 2 . DA is metabolised by monoamine oxidase (MAO) 3 , which catalyses th...
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Published in: | Nature (London) 1977-01, Vol.265 (5589), p.80-81 |
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Main Authors: | , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | DURING the past decade, the central neurotransmitter, dopamine (DA), has been much studied for it is known to be involved in certain human disease states, Parkinsonism
1
preeminently, and rather more inferentially, schizophrenia
2
. DA is metabolised by monoamine oxidase (MAO)
3
, which catalyses the oxidative deamination of a wide range of monoamines
4,5
, including the neurotransmitters noradrenaline (NA) and 5-hydroxytryptamine (5-HT), and other amines such as tyramine, tryptamine and phenylethylamine (PEA). On the basis of animal studies with the inhibitors, clorgyline
6
, and later deprenil
7
, MAO has been classified into two types, A and B. By definition, type A is selectively inhibited by clorgyline and type B by deprenil. In general, type A acts on 5-HT
6
while type B prefers PEA
8
. In the rat, DA is preferentially deaminated by MAOA
9–11
. It thus seemed paradoxical that, in the treatment of Parkinsonism, addition of the MAOB inhibitor, deprenil, to a DA-generating drug combination should produce further therapeutic benefit
12
. In this report, we reconcile these apparently conflicting observations by demonstrating that, as far as DA oxidation is concerned, man may be different from rat: in two sites we have investigated, platelet and brain, DA is preferentially deaminated by an enzyme with the characteristics of MAOB. |
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ISSN: | 0028-0836 1476-4687 |
DOI: | 10.1038/265080a0 |