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Effects of l‐Methyl‐4‐Phenyl‐l,2,3,6‐Tetrahydropyridine in the Dog: Effect of Pargyline Pretreatment
Author(s) -
Johannessen J. N.,
Chiueh C. C.,
Bacon J. P.,
Garrick N. A.,
Burns R. S.,
Weise V. K.,
Kopin I. J.,
Parisi J. E.,
Markey S. P.
Publication year - 1989
Publication title -
journal of neurochemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.75
H-Index - 229
eISSN - 1471-4159
pISSN - 0022-3042
DOI - 10.1111/j.1471-4159.1989.tb07373.x
Subject(s) - pargyline , mptp , dopamine , substantia nigra , endocrinology , medicine , chemistry , monoamine oxidase , pars compacta , tyrosine hydroxylase , dopaminergic , biology , biochemistry , enzyme
Adult beagle dogs of either sex were injected with 1‐methyl‐4‐phenyl‐1,2,3,6‐tetrahydropyridine (MPTP)‐HCl (2.5 mg/kg, i.v.) alone or after pretreatment with pargyline (5.0 mg/kg, s.c, twice), with pargyline alone, or were unin‐jected. Groups were killed 2 h, 3 weeks, or 3 months after injection, and several brain areas were assayed for biogenic amines and their synthetic and degradative enzymes. MPTP caused a massive and permanent loss of striatal dopamine, tyrosine hydroxylase, and 3,4‐dihydroxyphenylalanine decarboxylase activities and the loss of cells within the substantia nigra pars compacta. Dopamine and norepinephrine also were depleted to various degrees in cortex, olfactory bulb, and hypothalamus; however, dopamine β‐hydroxylase activity in cortex was normal. There was no cell loss in the ventral tegmental area or locus ceruleus. The activities of monoamine oxidase (MAO)‐A and MAO‐B in cortex and caudate were not affected by MPTP. Despite a permanent loss of the ni‐grostriatal system, the dogs exhibited only a transient hypokinesia lasting 1‐2 weeks. Pargyline pretreatment prevented the loss of striatal dopamine and cells from the substantia nigra, but did not prevent a prolonged but reversible decrease in the concentration of dopamine metabolites. It is argued that this apparent inhibition of MAO is due not to suicide inactivation of the enzyme by MPTP, but to reversible inhibition by accumulation of the pyridinium metabolite, 1‐methyl‐4‐phenylpyridinium, selectively in aminergic terminals.