Journal
NEUROBIOLOGY OF DISEASE
Volume 41, Issue 1, Pages 51-61Publisher
ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.nbd.2010.08.018
Keywords
L-DOPA; Basal ganglia; GABA release; cAMP; Hemiparkinsonism; Substantia nigra
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Funding
- CONACyT (Mexico) [50428-M]
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L-DOPA treatment induces abnormal involuntary movements (AIMS) in Parkinson's patients and experimental animals. We examined the relationship between the development of AlMs (dyskinesia) and changes in [H-3]-GABA release and cAMP signaling in striatonigral terminals of rats with unilateral 6-OHDA lesions. Analysis of AlMs scores in hemiparkinsonian rats treated with L-DOPA for 20 days was fitted by the sum of two Gaussian distributions showing the presence of two populations: one with mild and the other with severe dyskinesia. cAMP signaling was evaluated in the two populations by determining changes in cAMP formation, G alpha(olf) and adenylyl cyclase type V/VI levels. In animals that were not treated with L-DOPA, all the parameters were significantly increased in the denervated side. In the animals that had mild dyskinesia, L-DOPA treatment normalized these parameters. In contrast, in the animals in which L-DOPA treatment induced severe dyskinesia all the parameters, except for G alpha(olf) levels, were significantly higher in the denervated side. Similarly, D1-stimulated [H-3]-GABA release was not elevated in L-DOPA-treated animals with mild dyskinesia but was increased in animals with severe dyskinesia. Changes in G alpha(olf) and adenylyl cyclase type V/VI levels in the striatum paralleled the response in the SNr. The linkage between the changes in [H-3]-GABA release and cAMP activity was further evaluated with the selective adenylyl cyclase V/VI antagonist NKY80. This inhibitor blocked the increases of both [H-3]-GABA release and cAMP production. These results indicate that increased expression of adenylyl cyclase V/VI is a major determinant of increased GABAergic transmission in the substantia nigra pars reticulata of animals in which L-DOPA induces severe dyskinesia. (C) 2010 Elsevier Inc. All rights reserved.
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