HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Maladaptive plasticity of serotonin axon terminals in levodopa-induced dyskinesia.

AbstractOBJECTIVE:
Striatal serotonin projections have been implicated in levodopa-induced dyskinesia by providing an unregulated source of dopamine release. We set out to determine whether these projections are affected by levodopa treatment in a way that would favor the occurrence of dyskinesia.
METHODS:
As an index of terminal serotonin innervation density, we measured radioligand binding to the plasma membrane serotonin transporter (SERT) in levodopa-treated dyskinetic and nondyskinetic subjects, using brain tissue from both rat and monkey models of Parkinson disease as well as parkinsonian patients. In addition, striatal tissue from dyskinetic rats was used for morphological and ultrastructural analyses of serotonin axon terminals, and for studies of stimulated [³H]dopamine release.
RESULTS:
Across all conditions examined, striatal levels of SERT radioligand binding were significantly elevated in dyskinetic subjects compared to nondyskinetic cases. In the rat striatum, dyskinesiogenic levodopa treatment had induced sprouting of serotonin axon varicosities having a relatively high synaptic incidence. This response was associated with increased depolarization-induced [³H]dopamine release and with a stronger release potentiation by brain-derived neurotrophic factor.
INTERPRETATION:
This study provides the first evidence that L-dopa treatment induces sprouting of serotonin axon terminals, with an increased incidence of synaptic contacts, and a larger activity-dependent potentiation of dopamine release in the dopamine-denervated striatum. Treatment-induced plasticity of the serotonin innervation may therefore represent a previously unappreciated cause of altered dopamine dynamics. These results are important for understanding the mechanisms by which L-dopa pharmacotherapy predisposes to dyskinesia, and for defining biomarkers of motor complications in Parkinsons disease.
AuthorsDaniella Rylander, Martin Parent, Sean S O'Sullivan, Sandra Dovero, Andrew J Lees, Erwan Bezard, Laurent Descarries, M Angela Cenci
JournalAnnals of neurology (Ann Neurol) Vol. 68 Issue 5 Pg. 619-28 (Nov 2010) ISSN: 1531-8249 [Electronic] United States
PMID20882603 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Brain-Derived Neurotrophic Factor
  • Serotonin Plasma Membrane Transport Proteins
  • Serotonin
  • Levodopa
  • Oxidopamine
  • 1-Methyl-4-phenyl-1,2,3,6-tetrahydropyridine
  • Dopamine
Topics
  • 1-Methyl-4-phenyl-1,2,3,6-tetrahydropyridine
  • Aged
  • Animals
  • Brain-Derived Neurotrophic Factor (pharmacology)
  • Corpus Striatum (drug effects, metabolism, pathology, ultrastructure)
  • Disease Models, Animal
  • Dopamine (metabolism)
  • Dyskinesia, Drug-Induced (pathology)
  • Female
  • Humans
  • Levodopa (adverse effects)
  • Macaca fascicularis
  • Male
  • Neuronal Plasticity (drug effects)
  • Oxidopamine
  • Parkinson Disease (drug therapy, metabolism)
  • Presynaptic Terminals (drug effects, pathology, ultrastructure)
  • Radioligand Assay
  • Rats
  • Rats, Sprague-Dawley
  • Serotonin (metabolism)
  • Serotonin Plasma Membrane Transport Proteins (metabolism)

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: