Gangliosides and parkinsonism.
Identifieur interne : 001580 ( PubMed/Checkpoint ); précédent : 001579; suivant : 001581Gangliosides and parkinsonism.
Auteurs : M T Herrero [France] ; A. Kastner ; I. Perez-Ota O ; E C Hirsch ; M R Luquin ; F. Javoy-Agid ; J. Del Río ; J A Obeso ; Yves Agid [France]Source :
- Neurology [ 0028-3878 ] ; 1993.
English descriptors
- KwdEn :
- Animals, Cell Death (drug effects), G(M1) Ganglioside (therapeutic use), MPTP Poisoning, Macaca fascicularis, Mesencephalon (drug effects), Mesencephalon (pathology), Motor Activity (drug effects), Nerve Fibers (drug effects), Nerve Fibers (pathology), Parkinson Disease, Secondary (chemically induced), Parkinson Disease, Secondary (pathology), Parkinson Disease, Secondary (prevention & control).
- MESH :
- chemical , therapeutic use : G(M1) Ganglioside.
- chemically induced : Parkinson Disease, Secondary.
- drug effects : Cell Death, Mesencephalon, Motor Activity, Nerve Fibers.
- pathology : Mesencephalon, Nerve Fibers, Parkinson Disease, Secondary.
- prevention & control : Parkinson Disease, Secondary.
- Animals, MPTP Poisoning, Macaca fascicularis.
Abstract
The protective effect of GM1 ganglioside against nerve cell death induced by 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) was analyzed in monkey mesencephalon. Administration of GM1 before and during MPTP treatment improved motor performances compared with MPTP-treated animals that received saline rather than GM1. Postmortem analysis revealed that GM1 did not protect dopaminergic cell bodies from MPTP intoxication but resulted in an increased immunoreactivity of tyrosine hydroxylase in the perikarya and processes of the surviving neurons. These data suggest that GM1 may be potentially used as a palliative rather than a curative therapy in Parkinson's disease.
PubMed: 8413979
Affiliations:
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pubmed:8413979Le document en format XML
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<front><div type="abstract" xml:lang="en">The protective effect of GM1 ganglioside against nerve cell death induced by 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) was analyzed in monkey mesencephalon. Administration of GM1 before and during MPTP treatment improved motor performances compared with MPTP-treated animals that received saline rather than GM1. Postmortem analysis revealed that GM1 did not protect dopaminergic cell bodies from MPTP intoxication but resulted in an increased immunoreactivity of tyrosine hydroxylase in the perikarya and processes of the surviving neurons. These data suggest that GM1 may be potentially used as a palliative rather than a curative therapy in Parkinson's disease.</div>
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<Abstract><AbstractText>The protective effect of GM1 ganglioside against nerve cell death induced by 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) was analyzed in monkey mesencephalon. Administration of GM1 before and during MPTP treatment improved motor performances compared with MPTP-treated animals that received saline rather than GM1. Postmortem analysis revealed that GM1 did not protect dopaminergic cell bodies from MPTP intoxication but resulted in an increased immunoreactivity of tyrosine hydroxylase in the perikarya and processes of the surviving neurons. These data suggest that GM1 may be potentially used as a palliative rather than a curative therapy in Parkinson's disease.</AbstractText>
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