Oxidative Stress: A common denominator in the pathogenesis of amyotrophic lateral sclerosis

Research output: Contribution to journalReview article

84 Scopus citations

Abstract

Purpose of review: Amyotrophic lateral sclerosis, or Lou Gehrig disease, is a progressive neurodegenerative disease of adult onset characterized by a loss of motor neurons in the spinal cord and motor cortex. In the last several years, substantial progress has been made in defining the pathogenesis of motor neuron injury and relationships between disease mechanisms and the selective vulnerability of the motor neuron in both familial and sporadic forms of amyotrophic lateral sclerosis. Recent findings: Current theories have shifted from a neuron-centered pathology to a focus on the interaction between motor neurons and glia, and their respective contributions to pathways implicated in amyotrophic lateral sclerosis. Although multiple mechanisms clearly can contribute to the pathogenesis of motor neuron injury, recent advances suggest that oxidative stress may play a significant role in the amplification, and possibly the initiation, of disease. Summary: This article reviews the clinical aspects of amyotrophic lateral sclerosis and potential mechanisms of disease pathogenesis in the context of recent data supporting a major role for oxidative stress throughout the disease course. Evidence suggesting an important role for intercellular signaling is emphasized.

Original languageEnglish (US)
Pages (from-to)730-736
Number of pages7
JournalCurrent Opinion in Rheumatology
Volume15
Issue number6
DOIs
StatePublished - Nov 2003

Keywords

  • Amyotrophic lateral sclerosis
  • Excitotoxicity
  • Immune activation
  • Oxidative stress

ASJC Scopus subject areas

  • Rheumatology
  • Immunology

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