Serveur d'exploration sur la maladie de Parkinson

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Bilateral overactivation of the sensorimotor cortex in the unilateral rodent model of Parkinson's disease – a functional magnetic resonance imaging study

Identifieur interne : 001932 ( Main/Exploration ); précédent : 001931; suivant : 001933

Bilateral overactivation of the sensorimotor cortex in the unilateral rodent model of Parkinson's disease – a functional magnetic resonance imaging study

Auteurs : Galit Pelled [Israël] ; Hagai Bergman [Israël] ; Gadi Goelman [Israël]

Source :

RBID : ISTEX:43483459E27823002CED30579F6783ACDC0D5340

English descriptors

Abstract

Functional magnetic resonance imaging (fMRI) is used to investigate the basal ganglia (BG)–cortex circuit using a rat model of Parkinson's disease (PD). The model involves a unilateral destruction of the right substantia nigra by intranigral injection of the dopaminergic neurotoxin 6‐hydroxydopamine. Volume of cortical activity was measured by the blood oxygenation level‐dependent contrast method while applying electrical forepaw stimulation. The main findings are the following. (i) Contrary to the predictions of the classic model but in line with recent experimental results (positron emission tomography, fMRI and electrophysiology), an increased cortical activity in the sensorimotor cortex of PD rats compared with sham‐operated or normal rats was found. (ii) A diffuse neuronal activity at large cortical areas that were not related directly to the stimulation used, was observed. (iii) No difference was found between the lesion and the nonlesion hemispheres when the left or the right forepaw was stimulated; both cortices show significant overactivation of the sensorimotor cortices in addition to diffuse cortical activation. The last finding could be explained by either corticocortical connections or by bilateral BG–cortex connections. These finding suggest that the mutual influence of the two hemispheres is important in the pathophysiology of the BG–cortex circuit and might be crucial in predicting treatments.

Url:
DOI: 10.1046/j.0953-816x.2001.01866.x


Affiliations:


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