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STRIATAL TYROSINE HYDROXYLASE-POSITIVE NEURONS ARE ASSOCIATED WITH L-DOPA-INDUCED DYSKINESIA IN HEMIPARKINSONIAN MICE

Keber, U. (author)
Klietz, M. (author)
Carlsson, Thomas, 1977 (author)
Gothenburg University,Göteborgs universitet,Institutionen för neurovetenskap och fysiologi, sektionen för farmakologi,Institute of Neuroscience and Physiology, Department of Pharmacology
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Oertel, W. H. (author)
Weihe, E. (author)
Schafer, M. K. H. (author)
Hoglinger, G. U. (author)
Depboylu, C. (author)
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 (creator_code:org_t)
Elsevier BV, 2015
2015
English.
In: Neuroscience. - : Elsevier BV. - 0306-4522. ; 298, s. 302-317
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • L-3,4-Dihydroxyphenylalanine (L-DOPA) is the therapeutic gold standard in Parkinson's disease. However, long-term treatment is complicated by the induction of debilitating abnormal involuntary movements termed L-DOPA-induced dyskinesias (LIDs). Until today the underlying mechanisms of LID pathogenesis are not fully understood. The aim of this study was to reveal new factors, which may be involved in the induction of LID. We have focused on the expression of striatal tyrosine hydroxylase-positive (TH+) neurons, which are capable of producing either L-DOPA or dopamine (DA) in target areas of ventral midbrain DAergic neurons. To address this issue, a daily L-DOPA dose was administered over the course of 15 days to mice with unilateral 6-hydroxydopamine-induced lesions of the medial forebrain bundle and LIDs were evaluated. Remarkably, the number of striatal TH+ neurons strongly correlated with both induction and severity of LID as well as Delta FosB expression as an established molecular marker for LID. Furthermore, dyskinetic mice showed a marked augmentation of serotonergic fiber innervation in the striatum, enabling the decarboxylation of L-DOPA to DA. Axial, limb and orolingual dyskinesias were predominantly associated with TH+ neurons in the lateral striatum, whereas medially located TH+ neurons triggered locomotive rotations. In contrast, identified accumbal and cortical TH+ cells did not contribute to the generation of LID. Thus, striatal TH+ cells and serotonergic terminals may cooperatively synthesize DA and subsequently contribute to supraphysiological synaptic DA concentrations, an accepted cause in LID pathogenesis. (C) 2015 IBRO. Published by Elsevier Ltd. All rights reserved.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Neurovetenskaper (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Neurosciences (hsv//eng)

Keyword

Parkinson's disease
dopamine
abnormal involuntary movement
striatum
accumbens
TH
PARKINSONS-DISEASE PATIENTS
LEVODOPA-INDUCED DYSKINESIAS
DOPAMINERGIC-NEURONS
NUCLEUS-ACCUMBENS
RAT MODEL
FUNCTIONAL-SIGNIFICANCE
FOSB EXPRESSION
UP-REGULATION
DELTA-FOSB
IMMUNOREACTIVE NEURONS
Neurosciences
INSSEN EPM
1994
JOURNAL OF NEUROSCIENCE
V14
P1555
SHIRO Y
1989
NEUROSCIENCE LETTERS
V97
P6

Publication and Content Type

ref (subject category)
art (subject category)

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