Recovery of whisking function promoted by manual stimulation of the vibrissal muscles after facial nerve injury requires insulin-like growth factor 1 (IGF-1)

Exp Neurol. 2010 Apr;222(2):226-34. doi: 10.1016/j.expneurol.2009.12.031. Epub 2010 Jan 11.

Abstract

Recently, we showed that manual stimulation (MS) of denervated vibrissal muscles enhanced functional recovery following facial nerve cut and suture (FFA) by reducing poly-innervation at the neuro-muscular junctions (NMJ). Although the cellular correlates of poly-innervation are established, with terminal Schwann cells (TSC) processes attracting axon sprouts to "bridge" adjacent NMJ, molecular correlates are poorly understood. Since quantitative RT-PCR revealed a rapid increase of IGF-1 mRNA in denervated muscles, we examined the effect of daily MS for 2 months after FFA in IGF-1(+/-) heterozygous mice; controls were wild-type (WT) littermates including intact animals. We quantified vibrissal motor performance and the percentage of NMJ bridged by S100-positive TSC. There were no differences between intact WT and IGF-1(+/-) mice for vibrissal whisking amplitude (48 degrees and 49 degrees ) or the percentage of bridged NMJ (0%). After FFA and handling alone (i.e. no MS) in WT animals, vibrissal whisking amplitude was reduced (60% lower than intact) and the percentage of bridged NMJ increased (42% more than intact). MS improved both the amplitude of vibrissal whisking (not significantly different from intact) and the percentage of bridged NMJ (12% more than intact). After FFA and handling in IGF-1(+/-) mice, the pattern was similar (whisking amplitude 57% lower than intact; proportion of bridged NMJ 42% more than intact). However, MS did not improve outcome (whisking amplitude 47% lower than intact; proportion of bridged NMJ 40% more than intact). We conclude that IGF-I is required to mediate the effects of MS on target muscle reinnervation and recovery of whisking function.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Analysis of Variance
  • Animals
  • Disease Models, Animal
  • Facial Muscles / physiology*
  • Facial Nerve Injuries / pathology
  • Facial Nerve Injuries / rehabilitation*
  • Female
  • Functional Laterality / physiology
  • Gene Expression Regulation / physiology
  • Handling, Psychological
  • Insulin-Like Growth Factor I / deficiency
  • Insulin-Like Growth Factor I / metabolism*
  • Mice
  • Mice, Knockout
  • Movement / physiology
  • Physical Stimulation / methods*
  • Rats
  • Rats, Sprague-Dawley
  • Receptor, IGF Type 1 / metabolism
  • Receptors, Nicotinic / metabolism
  • Recovery of Function / physiology*
  • Regeneration / physiology
  • S100 Proteins / metabolism
  • Vibrissae / innervation
  • Vibrissae / physiology*

Substances

  • Receptors, Nicotinic
  • S100 Proteins
  • Insulin-Like Growth Factor I
  • Receptor, IGF Type 1