Literature DB >> 3874094

Metabolism of the neurotoxin in MPTP by human liver monoamine oxidase B.

R R Fritz, C W Abell, N T Patel, W Gessner, A Brossi.   

Abstract

The neurotoxin 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) was oxidized to dihydropyridine MPDP+ and pyridine MPP+ by preparations of monoamine oxidase B (MAO B), including pure human liver MAO B:monoclonal antibody complex, Km,app values for MPTP and benzylamine, a preferred MAO B substrate, were 316 and 64 microM, respectively. 4-Phenyl-1,2,3,6-tetrahydropyridine (PTP), the nor derivative of MPTP, was also a substrate (Km,app = 221 microM). MPDP+, MPTP, and MPP+, but not PTP, were found to be irreversible inhibitors of MAO B. Our studies support the hypothesis that MPTP is oxidized in primate brain by MAO B to MPDP+, which is then converted to MPP+, a major metabolite found in the substantia nigra.

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Year:  1985        PMID: 3874094     DOI: 10.1016/0014-5793(85)80713-4

Source DB:  PubMed          Journal:  FEBS Lett        ISSN: 0014-5793            Impact factor:   4.124


  13 in total

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2.  cDNA cloning of human liver monoamine oxidase A and B: molecular basis of differences in enzymatic properties.

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4.  Oxidation and enzyme-activated irreversible inhibition of rat liver monoamine oxidase-B by 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP).

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6.  An in vitro model of 1-methyl-4-phenyl-pyridinium (MPP+) toxicity: incubation of rabbit caudate nucleus slices with MPP+ followed by biochemical and functional analysis.

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7.  Mechanism-based inactivation of monoamine oxidases A and B by tetrahydropyridines and dihydropyridines.

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9.  In Vitro and in Vivo Neuroprotective Effects of Walnut (Juglandis Semen) in Models of Parkinson's Disease.

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10.  Characteristics of the mitochondrial and cellular uptake of MPP+, as probed by the fluorescent mimic, 4'I-MPP.

Authors:  Mapa S T Mapa; Viet Q Le; Kandatege Wimalasena
Journal:  PLoS One       Date:  2018-08-23       Impact factor: 3.240

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