Effect of locally delivered IGF-1 on nerve regeneration during aging: an experimental study in rats

Muscle Nerve. 2010 Mar;41(3):335-41. doi: 10.1002/mus.21485.

Abstract

Age is an important predictor of neuromuscular recovery after peripheral nerve injury. Insulin-like growth factor 1 (IGF-1) is a potent neurotrophic factor that is known to decline with increasing age. The purpose of this study was to determine if locally delivered IGF-1 would improve nerve regeneration and neuromuscular recovery in aged animals. Young and aged rats underwent nerve transection and repair with either saline or IGF-1 continuously delivered to the site of the nerve repair. After 3 months, nerve regeneration and neuromuscular junction morphology were assessed. In both young and aged animals, IGF-1 significantly improved axon number, diameter, and density. IGF-1 also significantly increased myelination and Schwann cell activity and preserved the morphology of the postsynaptic neuromuscular junction (NMJ). These results show that aged regenerating nerve is sensitive to IGF-1 treatment.

Publication types

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

MeSH terms

  • Age Factors
  • Aging / drug effects*
  • Aging / physiology
  • Analysis of Variance
  • Animals
  • Axons / drug effects
  • Axons / physiology
  • GAP-43 Protein / genetics
  • GAP-43 Protein / metabolism
  • Insulin-Like Growth Factor I / administration & dosage*
  • Muscle, Skeletal / drug effects
  • Muscle, Skeletal / metabolism
  • Muscle, Skeletal / physiology
  • Nerve Fibers, Myelinated / drug effects
  • Nerve Fibers, Myelinated / physiology
  • Nerve Regeneration / drug effects*
  • Nerve Regeneration / physiology
  • Neuromuscular Junction / drug effects
  • Neuromuscular Junction / physiology
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Rats
  • Reverse Transcriptase Polymerase Chain Reaction
  • Schwann Cells / drug effects
  • Schwann Cells / physiology
  • Tibial Nerve / drug effects*
  • Tibial Nerve / injuries*

Substances

  • GAP-43 Protein
  • RNA, Messenger
  • Insulin-Like Growth Factor I