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Abstract

Parkinson’s disease (PD) involves the degeneration of dopaminergic (DA) neurons in the substantia nigra pars compacta (SNc) that is thought to cause the classical motor symptoms of this disease. However, motivational and affective impairments are also often observed in PD patients. These are usually attributed to a psychological reaction to the general motor impairment and to a loss of some of the neurons within the ventral tegmental area (VTA). We induced selective lesions of the VTA and SNc DA neurons that did not provoke motor deficits, and showed that bilateral dopamine loss within the SNc, but not within the VTA, induces motivational deficits and affective impairments that mimicked the symptoms of PD patients. Thus, motivational and affective deficits are a core impairment of PD, as they stem from the loss of the major group of neurons that degenerates in this disease (DA SNc neurons) and are independent of motor deficits.

Details

Title
Loss of dopaminergic nigrostriatal neurons accounts for the motivational and affective deficits in Parkinson’s disease
Author
Drui, G 1 ; Carnicella, S 1 ; Carcenac, C 1 ; Favier, M 1 ; Bertrand, A 1 ; Boulet, S 1 ; Savasta, M 2 

 Institut National de la Santé et de la Recherche Médicale, Unité 836, Grenoble Institut des Neurosciences, Dynamique et Physiopathologie des Ganglions de la Base, Grenoble, France (GRID:grid.462307.4) (ISNI:0000 0004 0429 3736); Université Joseph Fourier, Grenoble, France (GRID:grid.9621.c) (ISNI:0000 0001 0944 2786) 
 Institut National de la Santé et de la Recherche Médicale, Unité 836, Grenoble Institut des Neurosciences, Dynamique et Physiopathologie des Ganglions de la Base, Grenoble, France (GRID:grid.462307.4) (ISNI:0000 0004 0429 3736); Université Joseph Fourier, Grenoble, France (GRID:grid.9621.c) (ISNI:0000 0001 0944 2786); Centre Hospitalier Universitaire de Grenoble, Grenoble, France (GRID:grid.410529.b) (ISNI:0000 0001 0792 4829) 
Pages
358-367
Publication year
2014
Publication date
Mar 2014
Publisher
Nature Publishing Group
ISSN
13594184
e-ISSN
14765578
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
2645770191
Copyright
© Macmillan Publishers Limited 2014.