Nogo-A inhibitory peptide (NEP1-40) increases pan-cadherin expression following mild cortical contusion injury in rats

Turk Neurosurg. 2008 Oct;18(4):356-65.

Abstract

Background: Nogo-A is a myelin-associated neurite outgrowth inhibitory protein that limits elongation of central nerve fibers, neuronal regeneration and plasticity. We investigated the effect of delivering an inhibitory peptide that neutralizes Nogo-A on neuronal recovery following mild cortical contusion injury.

Methods: 41 rats were allocated into the control and NEP1-40 treatment groups. PBS was applied following trauma over the parietal cortex after opening the dura in the control group. NEP1-40 solution was immediately applied following trauma after opening the dura in the treatment group. Each group was further divided into 3 subgroups and sacrificed on the third, eighth, and 21st days after injury. The brains were removed for analysis.

Results: Immunohistochemical staining of the injured cortex for pan-cadherin revealed a significant increase in staining in the NEP 1-40 treatment group at the 8th and 21st days after injury. Electron microscopic evaluation revealed better cytoarchitectural preservation in the axons of the animals treated with NEP 1-40.

Conclusion: We observed improved preservation of injured neurons after topical application of NEP 1-40 following mild cortical injury. Pan-cadherin expression may correlate with the recovery of neurons and axonal bodies. Electron microscopical findings confirmed better preservation of neuronal structures after NEP1-40 treatment. Pan-cadherin is a good marker for neuronal recovery after cortical injury.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Blood Pressure / physiology
  • Brain Injuries / drug therapy*
  • Brain Injuries / metabolism*
  • Brain Injuries / pathology
  • Cadherins / biosynthesis*
  • Cerebral Cortex / drug effects
  • Cerebral Cortex / injuries*
  • Humans
  • Immunohistochemistry
  • Male
  • Microscopy, Electron, Transmission
  • Myelin Proteins / pharmacology*
  • Neurons / drug effects
  • Neurons / metabolism
  • Peptide Fragments / pharmacology*
  • Rats
  • Rats, Sprague-Dawley
  • Recombinant Proteins / pharmacology
  • Recovery of Function

Substances

  • Cadherins
  • Myelin Proteins
  • NEP1-40 protein, human
  • Peptide Fragments
  • Recombinant Proteins