La maladie de Parkinson en France (serveur d'exploration)

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Chronic MPTP treatment reproduces in baboons the differential vulnerability of mesencephalic dopaminergic neurons observed in Parkinson's disease

Identifieur interne : 001933 ( PascalFrancis/Corpus ); précédent : 001932; suivant : 001934

Chronic MPTP treatment reproduces in baboons the differential vulnerability of mesencephalic dopaminergic neurons observed in Parkinson's disease

Auteurs : M. Varastet ; D. Riche ; M. Maziere ; P. Hantraye

Source :

RBID : Pascal:94-0715673

Descripteurs français

English descriptors

Abstract

Chronic administration of 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) to baboons was shown previously to result in a motor syndrome and a pattern of striatal dopaminergic fibre loss similar to those observed in idiopathic Parkinson's disease. In the present study, tyrosine hydroxylase-immunoreactive neurons were qwantified in the mesencephalon of control (n=4) and chronically MPTP-treated (n=3) baboons. MPTP induced a significant reduction in neuronal cell density in the substantia nigra (63.8% reduction) and the ventral tegmental area (53.1%). Within the substantia nigra, obvious mediolateral and dorsoventral gradients of neuronal cell loss were observed

Notice en format standard (ISO 2709)

Pour connaître la documentation sur le format Inist Standard.

pA  
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A03   1    @0 Neuroscience
A05       @2 63
A06       @2 1
A08 01  1  ENG  @1 Chronic MPTP treatment reproduces in baboons the differential vulnerability of mesencephalic dopaminergic neurons observed in Parkinson's disease
A11 01  1    @1 VARASTET (M.)
A11 02  1    @1 RICHE (D.)
A11 03  1    @1 MAZIERE (M.)
A11 04  1    @1 HANTRAYE (P.)
A14 01      @1 CEA CNRS, DRIPP, serv. hosp. Frédéric Joliot @2 91401 Orsay @3 FRA @Z 1 aut. @Z 3 aut. @Z 4 aut.
A14 02      @1 CNRS Inst. Alfred Fessard @2 91198 Gif-sur-Yvette @3 FRA @Z 2 aut.
A20       @1 47-56
A21       @1 1994
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C01 01    ENG  @0 Chronic administration of 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) to baboons was shown previously to result in a motor syndrome and a pattern of striatal dopaminergic fibre loss similar to those observed in idiopathic Parkinson's disease. In the present study, tyrosine hydroxylase-immunoreactive neurons were qwantified in the mesencephalon of control (n=4) and chronically MPTP-treated (n=3) baboons. MPTP induced a significant reduction in neuronal cell density in the substantia nigra (63.8% reduction) and the ventral tegmental area (53.1%). Within the substantia nigra, obvious mediolateral and dorsoventral gradients of neuronal cell loss were observed
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Format Inist (serveur)

NO : PASCAL 94-0715673 INIST
ET : Chronic MPTP treatment reproduces in baboons the differential vulnerability of mesencephalic dopaminergic neurons observed in Parkinson's disease
AU : VARASTET (M.); RICHE (D.); MAZIERE (M.); HANTRAYE (P.)
AF : CEA CNRS, DRIPP, serv. hosp. Frédéric Joliot/91401 Orsay/France (1 aut., 3 aut., 4 aut.); CNRS Inst. Alfred Fessard/91198 Gif-sur-Yvette/France (2 aut.)
DT : Publication en série; Niveau analytique
SO : Neuroscience; ISSN 0306-4522; Coden NRSCDN; Royaume-Uni; Da. 1994; Vol. 63; No. 1; Pp. 47-56; Bibl. 61 ref.
LA : Anglais
EA : Chronic administration of 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) to baboons was shown previously to result in a motor syndrome and a pattern of striatal dopaminergic fibre loss similar to those observed in idiopathic Parkinson's disease. In the present study, tyrosine hydroxylase-immunoreactive neurons were qwantified in the mesencephalon of control (n=4) and chronically MPTP-treated (n=3) baboons. MPTP induced a significant reduction in neuronal cell density in the substantia nigra (63.8% reduction) and the ventral tegmental area (53.1%). Within the substantia nigra, obvious mediolateral and dorsoventral gradients of neuronal cell loss were observed
CC : 002B17G
FD : Tyrosine 3-monooxygenase; Mésencéphale; Neurone dopaminergique; Parkinson maladie; Neurotoxine; Pathologie expérimentale; Animal; Singe; MPTP
FG : Oxidoreductases; Enzyme; Système nerveux central; Maladie dégénérative; Système nerveux pathologie; Primates; Mammalia; Vertebrata
ED : Tyrosine 3-monooxygenase; Midbrain; Dopaminergic neuron; Parkinson disease; Neurotoxin; Experimental disease; Animal; Monkey
EG : Oxidoreductases; Enzyme; Central nervous system; Degenerative disease; Nervous system diseases; Primates; Mammalia; Vertebrata
SD : Tyrosine 3-monooxygenase; Mesencéfalo; Neurona dopaminérgica; Parkinson enfermedad; Neurotoxina; Patología experimental; Animal; Mono
LO : INIST-17194.354000042107130050
ID : 94-0715673

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Pascal:94-0715673

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<s5>26</s5>
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<s0>Degenerative disease</s0>
<s5>26</s5>
</fC07>
<fC07 i1="04" i2="X" l="SPA">
<s0>Enfermedad degenerativa</s0>
<s5>26</s5>
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<s5>27</s5>
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<s0>Primates</s0>
<s2>NS</s2>
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<fC07 i1="06" i2="X" l="ENG">
<s0>Primates</s0>
<s2>NS</s2>
</fC07>
<fC07 i1="06" i2="X" l="SPA">
<s0>Primates</s0>
<s2>NS</s2>
</fC07>
<fC07 i1="07" i2="X" l="FRE">
<s0>Mammalia</s0>
<s2>NS</s2>
</fC07>
<fC07 i1="07" i2="X" l="ENG">
<s0>Mammalia</s0>
<s2>NS</s2>
</fC07>
<fC07 i1="07" i2="X" l="SPA">
<s0>Mammalia</s0>
<s2>NS</s2>
</fC07>
<fC07 i1="08" i2="X" l="FRE">
<s0>Vertebrata</s0>
<s2>NS</s2>
</fC07>
<fC07 i1="08" i2="X" l="ENG">
<s0>Vertebrata</s0>
<s2>NS</s2>
</fC07>
<fC07 i1="08" i2="X" l="SPA">
<s0>Vertebrata</s0>
<s2>NS</s2>
</fC07>
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<s1>353</s1>
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<NO>PASCAL 94-0715673 INIST</NO>
<ET>Chronic MPTP treatment reproduces in baboons the differential vulnerability of mesencephalic dopaminergic neurons observed in Parkinson's disease</ET>
<AU>VARASTET (M.); RICHE (D.); MAZIERE (M.); HANTRAYE (P.)</AU>
<AF>CEA CNRS, DRIPP, serv. hosp. Frédéric Joliot/91401 Orsay/France (1 aut., 3 aut., 4 aut.); CNRS Inst. Alfred Fessard/91198 Gif-sur-Yvette/France (2 aut.)</AF>
<DT>Publication en série; Niveau analytique</DT>
<SO>Neuroscience; ISSN 0306-4522; Coden NRSCDN; Royaume-Uni; Da. 1994; Vol. 63; No. 1; Pp. 47-56; Bibl. 61 ref.</SO>
<LA>Anglais</LA>
<EA>Chronic administration of 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) to baboons was shown previously to result in a motor syndrome and a pattern of striatal dopaminergic fibre loss similar to those observed in idiopathic Parkinson's disease. In the present study, tyrosine hydroxylase-immunoreactive neurons were qwantified in the mesencephalon of control (n=4) and chronically MPTP-treated (n=3) baboons. MPTP induced a significant reduction in neuronal cell density in the substantia nigra (63.8% reduction) and the ventral tegmental area (53.1%). Within the substantia nigra, obvious mediolateral and dorsoventral gradients of neuronal cell loss were observed</EA>
<CC>002B17G</CC>
<FD>Tyrosine 3-monooxygenase; Mésencéphale; Neurone dopaminergique; Parkinson maladie; Neurotoxine; Pathologie expérimentale; Animal; Singe; MPTP</FD>
<FG>Oxidoreductases; Enzyme; Système nerveux central; Maladie dégénérative; Système nerveux pathologie; Primates; Mammalia; Vertebrata</FG>
<ED>Tyrosine 3-monooxygenase; Midbrain; Dopaminergic neuron; Parkinson disease; Neurotoxin; Experimental disease; Animal; Monkey</ED>
<EG>Oxidoreductases; Enzyme; Central nervous system; Degenerative disease; Nervous system diseases; Primates; Mammalia; Vertebrata</EG>
<SD>Tyrosine 3-monooxygenase; Mesencéfalo; Neurona dopaminérgica; Parkinson enfermedad; Neurotoxina; Patología experimental; Animal; Mono</SD>
<LO>INIST-17194.354000042107130050</LO>
<ID>94-0715673</ID>
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