Abstract
The fundamental cause of idiopathic Parkinson’s disease (PD) has remained unknown since its original description in the 19th century. Despite this fact, a rational therapeutic approach (exogenous replacement of the missing neurotransmitter, dopamine) was successfully introduced by Cotzias in 1967 [1], following the conceptual framework of Carlsson in 1959 [2], who suggested that dopamine may be a transmitter in the central nervous system involved in the control of motor function and may be involved in the parkinsonian syndrome; and the impressive neurochemical data of Hornykiewicz in 1963 [3] which definitively demonstrated a significant reduction in nigrostriatal dopamine concentration in both idiopathic and postencephalitic Parkinson’s disease. Since then, the major therapeutic efforts have been primarily focused on modifications of the “delivery” of L-dopa [4–8], the use of dopamine agonists [9–12], and, more recently, the use of monoamine oxidase inhibitors, either alone or as adjuvants to levodopa therapy [13–18]. The latter therapeutic approach (specifically the use of a selective MAO-B inhibitor, selegiline (l-deprenyl) in combination with levodopa) is the focus of this review.
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Elizan, T.S. (1993). (—)-Deprenyl Combined with L-Dopa in the Treatment of Parkinson’s Disease. In: Szelenyi, I. (eds) Inhibitors of Monoamine Oxidase B. Milestones in Drug Therapy. Birkhäuser, Basel. https://doi.org/10.1007/978-3-0348-6348-3_14
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DOI: https://doi.org/10.1007/978-3-0348-6348-3_14
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