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Updated: Jul 18, 2026

A Quick Phenotypic Neurological Scoring System for Evaluating Disease Progression in the SOD1-G93A Mouse Model of ALS
Published on: October 6, 2015
Erythropoietin delays disease onset in an amyotrophic lateral sclerosis model
Jonathan F Grunfeld1, Yael Barhum, Netta Blondheim
1Department of Neurology, Asaf HaRofeh Medical Center, Tel Aviv University, Sackler School of Medicine, Israel. jonathangrunfeld@yahoo.com
Abstract:
Erythropoietin (Epo) has been shown in the recent years to have neuroprotective activity in a variety of settings. In this study, we investigated its impact on the progression of paralysis in a mouse model simulating the human disorder amyotrophic lateral sclerosis (ALS). We found that Epo can delay the onset of motor deterioration in transgenic SOD G93A mice without prolonging their survival. Notably this effect was selective for the females only. These initial findings encourage further investigation of this biological avenue in the search for improved remedies for this fatal disease.

