Synergy of insulin-like growth factor-1 and exercise in amyotrophic lateral sclerosis

Ann Neurol. 2005 May;57(5):649-55. doi: 10.1002/ana.20451.

Abstract

Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disease of the neuromuscular system resulting in paralysis and ultimately death. Currently, no effective therapy is prescribed for patients; however, several therapeutic strategies are showing promise. Either exercise or treatment with adeno-associated virus/insulin-like growth factor-1 alone has therapeutic benefits in an amyotrophic lateral sclerosis transgenic mouse model. We show here that activity duration affects the therapeutic benefit associated with exercise, with 6- and 12-hour exposure to a running wheel providing significant motor function benefits and increased survival. Remarkably, a combination of insulin-like growth factor-1 gene delivery and exercise has profound effects on survival and function, indicative of synergistic effects with exercise and insulin-like growth factor-1. Our results indicate that a drug treatment in combination with appropriate exercise may provide the most promising therapy for amyotrophic lateral sclerosis to date.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Aging / physiology
  • Amyotrophic Lateral Sclerosis / drug therapy
  • Amyotrophic Lateral Sclerosis / pathology
  • Amyotrophic Lateral Sclerosis / therapy*
  • Animals
  • Brain Chemistry / genetics
  • Cell Count
  • Dependovirus / genetics
  • Exercise Therapy*
  • Gene Expression
  • Genetic Therapy*
  • Heterozygote
  • Humans
  • Immunohistochemistry
  • Insulin-Like Growth Factor I / genetics*
  • Longevity
  • Mice
  • Mice, Transgenic
  • Motor Activity / physiology
  • Plasmids / genetics
  • Postural Balance / physiology
  • RNA / biosynthesis
  • RNA / genetics
  • Running
  • Spinal Cord / pathology
  • Superoxide Dismutase / genetics
  • Superoxide Dismutase-1
  • Survival Analysis

Substances

  • SOD1 protein, human
  • RNA
  • Insulin-Like Growth Factor I
  • Sod1 protein, mouse
  • Superoxide Dismutase
  • Superoxide Dismutase-1