Review: Therapeutic options for continuous dopaminergic stimulation in Parkinson's disease

Treatment of Parkinson's disease aims to replace dopaminergic transmission at striatal synapses. In the normal state, nigral neurons fire continuously, exposing striatal dopamine receptors to relatively constant levels of dopamine. In the disease state, periodic dosing and the short half-life o...

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Main Authors: O.K. Sujith, Carol Lane
Format: Article
Language:English
Published: SAGE Publishing 2009-03-01
Series:Therapeutic Advances in Neurological Disorders
Online Access:https://doi.org/10.1177/1756285608101378
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spelling doaj-c338a06dd15d491e9999471cc8779a5b2020-11-25T03:23:29ZengSAGE PublishingTherapeutic Advances in Neurological Disorders1756-28562009-03-01210.1177/1756285608101378Review: Therapeutic options for continuous dopaminergic stimulation in Parkinson's diseaseO.K. SujithCarol LaneTreatment of Parkinson's disease aims to replace dopaminergic transmission at striatal synapses. In the normal state, nigral neurons fire continuously, exposing striatal dopamine receptors to relatively constant levels of dopamine. In the disease state, periodic dosing and the short half-life of antiparkinsonian drugs leads to more intermittent stimulation. Abnormal pulsatile stimulation of striatal dopamine receptors may lead to dysregulation of genes and proteins in downstream neurons and consequently, alterations in neuronal firing patterns. This may ultimately lead to motor complications. In order to prevent the development of motor complications a therapy that provides continuous dopaminergic stimulation as observed in the normal state would be ideal. Different routes of administration of levodopa and other dopaminergic drugs have been tried to achieve continuous dopaminergic stimulation (CDS). This review discusses the various methods available to achieve this goal with particular emphasis on duodenal dopa administration.https://doi.org/10.1177/1756285608101378
collection DOAJ
language English
format Article
sources DOAJ
author O.K. Sujith
Carol Lane
spellingShingle O.K. Sujith
Carol Lane
Review: Therapeutic options for continuous dopaminergic stimulation in Parkinson's disease
Therapeutic Advances in Neurological Disorders
author_facet O.K. Sujith
Carol Lane
author_sort O.K. Sujith
title Review: Therapeutic options for continuous dopaminergic stimulation in Parkinson's disease
title_short Review: Therapeutic options for continuous dopaminergic stimulation in Parkinson's disease
title_full Review: Therapeutic options for continuous dopaminergic stimulation in Parkinson's disease
title_fullStr Review: Therapeutic options for continuous dopaminergic stimulation in Parkinson's disease
title_full_unstemmed Review: Therapeutic options for continuous dopaminergic stimulation in Parkinson's disease
title_sort review: therapeutic options for continuous dopaminergic stimulation in parkinson's disease
publisher SAGE Publishing
series Therapeutic Advances in Neurological Disorders
issn 1756-2856
publishDate 2009-03-01
description Treatment of Parkinson's disease aims to replace dopaminergic transmission at striatal synapses. In the normal state, nigral neurons fire continuously, exposing striatal dopamine receptors to relatively constant levels of dopamine. In the disease state, periodic dosing and the short half-life of antiparkinsonian drugs leads to more intermittent stimulation. Abnormal pulsatile stimulation of striatal dopamine receptors may lead to dysregulation of genes and proteins in downstream neurons and consequently, alterations in neuronal firing patterns. This may ultimately lead to motor complications. In order to prevent the development of motor complications a therapy that provides continuous dopaminergic stimulation as observed in the normal state would be ideal. Different routes of administration of levodopa and other dopaminergic drugs have been tried to achieve continuous dopaminergic stimulation (CDS). This review discusses the various methods available to achieve this goal with particular emphasis on duodenal dopa administration.
url https://doi.org/10.1177/1756285608101378
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