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Journal ArticleDOI

Overview of present day treatment of Parkinson's disease.

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TLDR
Preliminary results in 35 patients indicate that Deprenyl, an MAO-B inhibitor, given with levodopa and carbidopa has shown the most promise and appears to be a valuable adjunctive agent for the long-term problem patient.
Abstract
In the light of present day knowledge, augmenting striatal dopaminergic activity is the most effective means for controlling the symptoms of parkinsonism. This is best accomplished by the administration of levodopa with a peripheral decarboxylase inhibitor. However, limitations in its benefits develop after long-term administration in a substantial number of patients. In an attempt to overcome these a number of pharmacological agents acting on striatal dopaminergic mechanisms have undergone clinical trial. Of those tried Deprenyl, an MAO-B inhibitor, given with levodopa and carbidopa has shown the most promise. Preliminary results in 35 patients indicate that it is useful in diminishing the incidence of “on-off” phenomena—one of the most limiting reactions to levodopa—as well as enabling some patients to recoup their loss of therapeutic benefits. Though far from resolving all of the therapeutic difficulties encountered with prolonged use of levodopa, it appears to be a valuable adjunctive agent for the long-term problem patient.

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Citations
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Journal ArticleDOI

Pargyline prevents MPTP-induced parkinsonism in primates.

TL;DR: Treatment of squirrel monkeys with pargyline prevents both clinical and neuropathological evidence of the neurotoxic effects of MPTP, and it is proposed that the conversion of MP TP to MPP+, possibly involving MAO, may be important for the neurot toxic effects to take place, and MPTP itself may not be the neurotoxicity agent.
Journal ArticleDOI

Increased life expectancy resulting from addition of l-deprenyl to Madopar® treatment in Parkinson's disease: A longterm study

TL;DR: Results are interpreted as indicating l-deprenyl's ability to prevent or retard the degeneration of striatal dopaminergic neurons, the first anti-Parkinson drug having such a property.
Journal ArticleDOI

MPTP Toxicity: Implications for Research in Parkinson's Disease

TL;DR: The parkinsonism induced by MPTP in man closely resembles time-telescoped Parkinson's disease and it is hoped that an understanding of the mechanism of species specificity and cellular toxicity will in time explain the pathogenesis of idiopathic Parkinson's Disease and suggest new opportunities for effective therapy.
Journal ArticleDOI

Monoamine oxidase activity and monoamine metabolism in brains of parkinsonian patients treated with l-deprenyl.

TL;DR: The data indicate that the therapeutic actions of l‐deprenyl may lie in its selective inhibition of MAO‐B resulting in increased brain levels of DA formed from L‐dihydroxyphenylacetic acid (L‐DOPA).
Book ChapterDOI

Animal models of parkinsonism using selective neurotoxins: clinical and basic implications.

TL;DR: The interplay between the laboratory and the clinic in analyzing the biological bases of parkinsonism arid formulating a rational approach to its treatment is discussed, with a focus on animal models involving 6HDA and MPTP.
References
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Journal ArticleDOI

Success and problems of long-term levodopa therapy in Parkinson's disease.

TL;DR: It is concluded that progression of the underlying pathology of the disease is probably responsible for loss of benefit in patients on chronic levodopa therapy and discovery of the exact causes may provide a rational basis for new therapy.
Journal ArticleDOI

Treatment of parkinsonism with levodopa.

TL;DR: Under the most optimal circumstances, the best that can be expected from their judicious administration is a 20% reduction in the severity of symptoms with a modest improvement of functional capacity.
Journal Article

The neurochemistry of Parkinson's disease: effect of L-dopa therapy.

TL;DR: It was concluded that L-dopa's principal therapeutic effects in Parkinson's disease are consistent with its transformation to DA in the striatum.
Journal ArticleDOI

The potentiation of the anti akinetic effect after L-dopa treatment by an inhibitor of MAO-B, Deprenil.

TL;DR: Deprenil is an inhibitor of MAO-B and is characterized by less frequent side effects, which can be eliminated by lowering the dosage of Deprenil, which is an excellent drug for preventing these.
Journal ArticleDOI

Deprenyl in parkinson's disease

TL;DR: In this article, (-)-deprenyl, a fast-acting selective monoamine-oxidase-B inhibitor without a "cheese effect", was given to 41 patients with idiopathic Parkinson's disease who were receiving maximum tolerated doses of levodopa either alone or combined with carbidopa ("Sinemet").
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