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Effects of complete and partial lesions of the dopaminergic mesotelencephalic system on skilled forelimb use in the rat

Identifieur interne : 001165 ( Istex/Corpus ); précédent : 001164; suivant : 001166

Effects of complete and partial lesions of the dopaminergic mesotelencephalic system on skilled forelimb use in the rat

Auteurs : P. Barnéoud ; S. Parmentier ; M. Mazadier ; J. M. Miquet ; A. Boireau ; P. Dubédat ; J.-C. Blanchard

Source :

RBID : ISTEX:88F30D08C9B0F050F665BCBA52C0A90643D2405A

English descriptors

Abstract

Abstract: This study compares certain behavioural consequences of partial and complete unilateral lesions of the dopaminergic mesotelencephalic system. We investigated skilled forelimb use, rotations induced by apomorphine and amphetamine, and dopaminergic metabolism of the nigrostriatal system of rats that had received a unilateral injection of 6-hydroxydopamine into the medial forebrain bundle. The rats classified Apo(+), that rotated after the administrations of apomorphine, had a complete lesion of the nigrostriatal system, whereas those classified Apo(−), that did not rotate after the administration of apomorphine, had a partial lesion of the nigrostriatal system. In the Apo(+) rats, 99.8% of the dopamine in the striatum was depleted, as was 85% of that in the substantia nigra. For the Apo(−) rats, 72% of the dopamine in the striatum was depleted as was 56% of that in the substantia nigra. When investigated with the staircase test, the animals with the most severe dopamine depletions were those most impaired in the paw reaching task. Complete and partial unilateral depletions of the dopaminergic mesotelencephalic system impaired the heirarhic phases of paw reaching differently. A complete dopamine depletion, but not a partial one, decreased the number of attempts made with the contralateral paw, and induced a bias towards the ipsilateral paw. A partial dopamine lesion impaired the sensorimotor co-ordination of both paws, whereas the complete dopamine lesion had a greater effect on the contralateral paw than on the ipsilateral paw.The mild paw reaching impairments observed in animals with moderate depletions of dopamine are proposed as a model of the early symptoms of Parkinson's disease that may be useful for the development of protective or restorative therapies.

Url:
DOI: 10.1016/0306-4522(95)00112-V

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ISTEX:88F30D08C9B0F050F665BCBA52C0A90643D2405A

Le document en format XML

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<div type="abstract" xml:lang="en">Abstract: This study compares certain behavioural consequences of partial and complete unilateral lesions of the dopaminergic mesotelencephalic system. We investigated skilled forelimb use, rotations induced by apomorphine and amphetamine, and dopaminergic metabolism of the nigrostriatal system of rats that had received a unilateral injection of 6-hydroxydopamine into the medial forebrain bundle. The rats classified Apo(+), that rotated after the administrations of apomorphine, had a complete lesion of the nigrostriatal system, whereas those classified Apo(−), that did not rotate after the administration of apomorphine, had a partial lesion of the nigrostriatal system. In the Apo(+) rats, 99.8% of the dopamine in the striatum was depleted, as was 85% of that in the substantia nigra. For the Apo(−) rats, 72% of the dopamine in the striatum was depleted as was 56% of that in the substantia nigra. When investigated with the staircase test, the animals with the most severe dopamine depletions were those most impaired in the paw reaching task. Complete and partial unilateral depletions of the dopaminergic mesotelencephalic system impaired the heirarhic phases of paw reaching differently. A complete dopamine depletion, but not a partial one, decreased the number of attempts made with the contralateral paw, and induced a bias towards the ipsilateral paw. A partial dopamine lesion impaired the sensorimotor co-ordination of both paws, whereas the complete dopamine lesion had a greater effect on the contralateral paw than on the ipsilateral paw.The mild paw reaching impairments observed in animals with moderate depletions of dopamine are proposed as a model of the early symptoms of Parkinson's disease that may be useful for the development of protective or restorative therapies.</div>
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<ce:simple-para>This study compares certain behavioural consequences of partial and complete unilateral lesions of the dopaminergic mesotelencephalic system. We investigated skilled forelimb use, rotations induced by apomorphine and amphetamine, and dopaminergic metabolism of the nigrostriatal system of rats that had received a unilateral injection of 6-hydroxydopamine into the medial forebrain bundle. The rats classified Apo(+), that rotated after the administrations of apomorphine, had a complete lesion of the nigrostriatal system, whereas those classified Apo(−), that did not rotate after the administration of apomorphine, had a partial lesion of the nigrostriatal system. In the Apo(+) rats, 99.8% of the dopamine in the striatum was depleted, as was 85% of that in the substantia nigra. For the Apo(−) rats, 72% of the dopamine in the striatum was depleted as was 56% of that in the substantia nigra. When investigated with the staircase test, the animals with the most severe dopamine depletions were those most impaired in the paw reaching task. Complete and partial unilateral depletions of the dopaminergic mesotelencephalic system impaired the heirarhic phases of paw reaching differently. A complete dopamine depletion, but not a partial one, decreased the number of attempts made with the contralateral paw, and induced a bias towards the ipsilateral paw. A partial dopamine lesion impaired the sensorimotor co-ordination of both paws, whereas the complete dopamine lesion had a greater effect on the contralateral paw than on the ipsilateral paw.</ce:simple-para>
<ce:simple-para>The mild paw reaching impairments observed in animals with moderate depletions of dopamine are proposed as a model of the early symptoms of Parkinson's disease that may be useful for the development of protective or restorative therapies.</ce:simple-para>
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<ce:surname>Abrous</ce:surname>
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<title>Effects of complete and partial lesions of the dopaminergic mesotelencephalic system on skilled forelimb use in the rat</title>
</titleInfo>
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<title>Effects of complete and partial lesions of the dopaminergic mesotelencephalic system on skilled forelimb use in the rat</title>
</titleInfo>
<name type="personal">
<namePart type="given">P.</namePart>
<namePart type="family">Barnéoud</namePart>
<affiliation>Rhoˆne-Poulenc Rorer S.A., Centre de Recherches de Vitry-Alfortville, Département de Biologie, 13 quai Jules Guesde, F-94403, Vitry-sur-Seine Cedex, France</affiliation>
<description>To whom correspondence should be addressed.</description>
<role>
<roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal">
<namePart type="given">S.</namePart>
<namePart type="family">Parmentier</namePart>
<affiliation>Rhoˆne-Poulenc Rorer S.A., Centre de Recherches de Vitry-Alfortville, Département de Biologie, 13 quai Jules Guesde, F-94403, Vitry-sur-Seine Cedex, France</affiliation>
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<namePart type="family">Miquet</namePart>
<affiliation>Rhoˆne-Poulenc Rorer S.A., Centre de Recherches de Vitry-Alfortville, Département de Biologie, 13 quai Jules Guesde, F-94403, Vitry-sur-Seine Cedex, France</affiliation>
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<name type="personal">
<namePart type="given">A.</namePart>
<namePart type="family">Boireau</namePart>
<affiliation>Rhoˆne-Poulenc Rorer S.A., Centre de Recherches de Vitry-Alfortville, Département de Biologie, 13 quai Jules Guesde, F-94403, Vitry-sur-Seine Cedex, France</affiliation>
<role>
<roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal">
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<namePart type="family">Dubédat</namePart>
<affiliation>Rhoˆne-Poulenc Rorer S.A., Centre de Recherches de Vitry-Alfortville, Département de Biologie, 13 quai Jules Guesde, F-94403, Vitry-sur-Seine Cedex, France</affiliation>
<role>
<roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal">
<namePart type="given">J.-C.</namePart>
<namePart type="family">Blanchard</namePart>
<affiliation>Rhoˆne-Poulenc Rorer S.A., Centre de Recherches de Vitry-Alfortville, Département de Biologie, 13 quai Jules Guesde, F-94403, Vitry-sur-Seine Cedex, France</affiliation>
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<copyrightDate encoding="w3cdtf">1995</copyrightDate>
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<abstract lang="en">Abstract: This study compares certain behavioural consequences of partial and complete unilateral lesions of the dopaminergic mesotelencephalic system. We investigated skilled forelimb use, rotations induced by apomorphine and amphetamine, and dopaminergic metabolism of the nigrostriatal system of rats that had received a unilateral injection of 6-hydroxydopamine into the medial forebrain bundle. The rats classified Apo(+), that rotated after the administrations of apomorphine, had a complete lesion of the nigrostriatal system, whereas those classified Apo(−), that did not rotate after the administration of apomorphine, had a partial lesion of the nigrostriatal system. In the Apo(+) rats, 99.8% of the dopamine in the striatum was depleted, as was 85% of that in the substantia nigra. For the Apo(−) rats, 72% of the dopamine in the striatum was depleted as was 56% of that in the substantia nigra. When investigated with the staircase test, the animals with the most severe dopamine depletions were those most impaired in the paw reaching task. Complete and partial unilateral depletions of the dopaminergic mesotelencephalic system impaired the heirarhic phases of paw reaching differently. A complete dopamine depletion, but not a partial one, decreased the number of attempts made with the contralateral paw, and induced a bias towards the ipsilateral paw. A partial dopamine lesion impaired the sensorimotor co-ordination of both paws, whereas the complete dopamine lesion had a greater effect on the contralateral paw than on the ipsilateral paw.The mild paw reaching impairments observed in animals with moderate depletions of dopamine are proposed as a model of the early symptoms of Parkinson's disease that may be useful for the development of protective or restorative therapies.</abstract>
<subject lang="en">
<topic>DA : dopamine</topic>
<topic>EDTA : ethylenediaminetetra acetate</topic>
<topic>HVA : homovanillic acid</topic>
<topic>SH : sham-operated</topic>
<topic>6-OHDA : 6-hydroxydopamine</topic>
</subject>
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<titleInfo>
<title>Neuroscience</title>
</titleInfo>
<titleInfo type="abbreviated">
<title>NSC</title>
</titleInfo>
<genre type="journal">journal</genre>
<originInfo>
<dateIssued encoding="w3cdtf">199508</dateIssued>
</originInfo>
<identifier type="ISSN">0306-4522</identifier>
<identifier type="PII">S0306-4522(00)X0024-3</identifier>
<part>
<date>199508</date>
<detail type="volume">
<number>67</number>
<caption>vol.</caption>
</detail>
<detail type="issue">
<number>4</number>
<caption>no.</caption>
</detail>
<extent unit="issue pages">
<start>777</start>
<end>1020</end>
</extent>
<extent unit="pages">
<start>837</start>
<end>848</end>
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<identifier type="DOI">10.1016/0306-4522(95)00112-V</identifier>
<identifier type="PII">0306-4522(95)00112-V</identifier>
<identifier type="ArticleID">9500112V</identifier>
<accessCondition type="use and reproduction" contentType="copyright">©1995 IBRO</accessCondition>
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Wicri

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