Therapeutic Neuroprotective Agents For Amyotrophic Lateral Sclerosis
Department
neurobiology
Document Type
Article
Abstract
Amyotrophic lateral sclerosis (ALS) is a fatal chronic neurodegenerative disease whose hallmark is proteinaceous, ubiquitinated, cytoplasmic inclusions in motor neurons and surrounding cells. Multiple mechanisms proposed as responsible for ALS pathogenesis include dysfunction of protein degradation, glutamate excitotoxicity, mitochondrial dysfunction, apoptosis, oxidative stress, and inflammation. It is therefore essential to gain a better understanding of the underlying disease etiology and search for neuroprotective agents that might delay disease onset, slow progression, prolong survival, and ultimately reduce the burden of disease. Because riluzole, the only Food and Drug Administration (FDA)-approved treatment, prolongs the ALS patient's life by only 3 months, new therapeutic agents are urgently needed. In this review, we focus on studies of various small pharmacological compounds targeting the proposed pathogenic mechanisms of ALS and discuss their impact on disease progression. © 2013 Springer Basel.
Publication Date
12-1-2013
Publication Title
Cellular and Molecular Life Sciences
ISSN
1420682X
Volume
70
Issue
24
First Page
4729
Last Page
4745
Digital Object Identifier (DOI)
10.1007/s00018-013-1415-0
Recommended Citation
Pandya, Rachna S.; Zhu, Haining; Li, Wei; Bowser, Robert; Friedlander, Robert M.; and Wang, Xin, "Therapeutic Neuroprotective Agents For Amyotrophic Lateral Sclerosis" (2013). Translational Neuroscience. 39.
https://scholar.barrowneuro.org/neurobiology/39