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dc.contributor.authorDonnan, Geoffrey Aen
dc.contributor.authorWoodhouse, D Gen
dc.contributor.authorKaczmarczyk, S Jen
dc.contributor.authorHolder, J Een
dc.contributor.authorPaxinos, Gen
dc.contributor.authorChilco, P Jen
dc.contributor.authorChurchyard, A Jen
dc.contributor.authorKalnins, Renate Men
dc.contributor.authorFabinyi, Gavinen
dc.contributor.authorMendelsohn, Frederick AOen
dc.date.accessioned2015-05-15T23:58:56Z
dc.date.available2015-05-15T23:58:56Z
dc.date.issued1991-05-16en
dc.identifier.citationMolecular Neurobiology; 5(2-4): 421-33en
dc.identifier.govdoc1823144en
dc.identifier.otherPUBMEDen
dc.identifier.urihttp://ahro.austin.org.au/austinjspui/handle/1/10514en
dc.description.abstractA series of compensatory mechanisms within the dopaminergic system have been shown to maintain clinical function in the presence of dopamine loss. Experimental evidence for increased presynaptic dopamine turnover owing to increased dopamine synthesis, release, and reduced reuptake exists. Direct evidence that these mechanisms maintain extracellular dopamine levels is provided by intracerebral microdialysis techniques. Postsynaptic denervation supersensitivity clearly occurs with D2 dopamine receptors, although this is less evident with D1 receptors. Similarly, mechanisms of plasticity have been shown to be relevant in human postmortem and Positron Emission Tomographic studies of patients with Parkinson's disease. However, although presynaptic increases in dopamine turnover are well documented, postsynaptic D1 and D2 receptor changes have been more difficult to establish, mainly because of methodological difficulties. D2, but not D1, receptor increases have been documented in drug naive Parkinsonian patients with PET techniques. In transplantation of adrenal gland to striatum in animal models and patients with Parkinsonism where clinical improvement occurs, plasticity of host response may be as important as plasticity of the graft. Although some elements of the compensatory mechanism of dopamine plasticity may be deleterious, such as dyskinesias owing to dopamine receptor supersensitivity, the overall effect of delay and minimization of the clinical expression of disease is advantageous. An even greater understanding of the mechanisms involved may assist in developing future therapeutic strategies.en
dc.language.isoenen
dc.subject.otherAdrenal Glands.transplantationen
dc.subject.otherAdulten
dc.subject.otherAgeden
dc.subject.otherAnimalsen
dc.subject.otherCorpus Striatum.metabolism.physiopathology.radionuclide imagingen
dc.subject.otherDenervationen
dc.subject.otherDopamine.metabolism.physiologyen
dc.subject.otherHumansen
dc.subject.otherMiceen
dc.subject.otherMice, Inbred C57BLen
dc.subject.otherMiddle Ageden
dc.subject.otherNeuronal Plasticityen
dc.subject.otherNeurotoxins.toxicityen
dc.subject.otherParkinson Disease.metabolism.physiopathology.radionuclide imaging.surgeryen
dc.subject.otherParkinson Disease, Secondary.metabolism.physiopathology.surgeryen
dc.subject.otherRatsen
dc.subject.otherReceptors, Dopamine.metabolism.physiologyen
dc.subject.otherSynapses.physiologyen
dc.subject.otherTomography, Emission-Computeden
dc.subject.otherTransplantation, Heterotopicen
dc.titleEvidence for plasticity of the dopaminergic system in parkinsonism.en
dc.typeJournal Articleen
dc.identifier.journaltitleMolecular neurobiologyen
dc.identifier.affiliationDepartment of Neurology, Austin Hospital, Heidelberg, Victoria, Australiaen
dc.description.pages421-33en
dc.relation.urlhttp://www.ncbi.nlm.nih.gov/pubmed/1823144en
Appears in Collections:Journal articles

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