| Literature DB >> 14506714 |
Hafedh Haddad1, Carmen Cifuentes-Diaz, Audrey Miroglio, Natacha Roblot, Vandana Joshi, Judith Melki.
Abstract
Spinal muscular atrophy (SMA) is a motor neuron disease caused by mutations of the survival motor neuron 1 gene (SMN1). No curative treatment is available. Mutant mice carrying homozygous deletion of Smn exon 7 directed to neurons display a degenerative process of motor neurons similar to that found in human SMA. To test whether riluzole, which exhibits neurotrophic properties, might have a protective role in SMA, mutant mice were treated with it after the onset of the degenerative process. Riluzole improved median survival and exerted a protective effect against aberrant cytoskeletal organization of motor synaptic terminals but not against loss of proximal axons. These results demonstrate that the disease course of SMA can be attenuated after the onset of neuromuscular defects and may warrant further investigation in a therapeutic trial in SMA.Entities:
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Year: 2003 PMID: 14506714 DOI: 10.1002/mus.10455
Source DB: PubMed Journal: Muscle Nerve ISSN: 0148-639X Impact factor: 3.217