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Benefit of tianeptine and morphine in a transgenic model of familial amyotrophic lateral sclerosis

Authors :
Gérard Besson
Marc Savasta
M. Chritin
Département de neurologie
Université Joseph Fourier - Grenoble 1 (UJF)-CHU Grenoble
Dynamique des Reseaux Neuronaux
Université Joseph Fourier - Grenoble 1 (UJF)-Institut National de la Santé et de la Recherche Médicale (INSERM)
Collaboration
Savasta, Marc
Source :
Amyotroph Lateral Scler, Amyotroph Lateral Scler, 2006, 7 (1), pp.32-7. ⟨10.1080/14660820510012022⟩
Publication Year :
2006
Publisher :
Informa UK Limited, 2006.

Abstract

International audience; The familial form of amyotrophic lateral sclerosis (FALS) has been linked in some cases to dominant mutations in the gene encoding the Cu/Zn superoxide dismutase (SOD1) mutation. Transgenic mice bearing the G93A SOD1 mutation develop clinical symptoms and pathological features similar to those described in the human disease and represent a good model to explore the potential benefit of therapeutic agents. Using this animal model, we tested the efficacy of morphine and tianeptine treatments, separately and in association, on both disease progression and survival. Acute injection of either of them, administered daily and before the onset of the disease, significantly prolonged the survival of the transgenic mice.

Details

ISSN :
1471180X and 17482968
Volume :
7
Database :
OpenAIRE
Journal :
Amyotrophic Lateral Sclerosis
Accession number :
edsair.doi.dedup.....e9968f5bb8c7d544302c8289db139fd9
Full Text :
https://doi.org/10.1080/14660820510012022