Hyperbaric oxygen preconditioning promotes survival of retinal ganglion cells in a rat model of optic nerve crush

J Neurotrauma. 2010 Apr;27(4):763-70. doi: 10.1089/neu.2009.1005.

Abstract

In this study we tested the hypothesis that hyperbaric oxygen preconditioning (HBO-PC) reduces retinal neuronal death due to optic nerve crush (ONC). Adult male Sprague-Dawley rats were subjected to ONC accompanied by a contralateral sham operation. HBO-PC was conducted four times by giving 100% oxygen at 2.5 atmospheres absolute (ATA) for 1 h every 12 h for 2 days prior to ONC. The rats were euthanized at 1 or 2 weeks after ONC. Retinal ganglion cell (RGC) density was counted by hematoxylin and eosin (H&E) staining of the retina and retrograde labeling with FluoroGold application to the superior colliculus. Visual function was assessed by flash visual evoked potentials (FVEP). TUNEL straining and caspase-3 and caspase-9 activity in the retinas were assessed. The RGC density in the retinas of ONC HBO-PC-treated rats was significantly higher than that of the corresponding ONC-only rats (the survival rate was 67.2% versus 49.7% by H&E staining, and 60.3% versus 28.9% by retrograde labeling with FluoroGold, respectively; p < 0.01) at 2 weeks after ONC. FVEP measurements indicated a significantly better preserved latency and amplitude of the P1 wave in the ONC HBO-PC-treated rats than the ONC-only rats (92 +/- 7 msec, 21 +/- 3 microv in the sham-operated group, 117 +/- 12 msec, 14 +/- 2 microv in the HBO-PC-treated group, and 169 +/- 15 msec, 7 +/- 1 microv in the corresponding ONC group; p < 0.01). TUNEL assays showed fewer apoptotic cells in the HBO-PC-treated group, accompanied by the suppression of caspase-3 and caspase-9 activity. These results demonstrate that HBO-PC appears to be neuroprotective against ONC insult via inhibition of neuronal apoptosis pathways.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Apoptosis / physiology
  • Axons / physiology
  • Axons / ultrastructure
  • Caspase 3 / metabolism
  • Caspase 9 / metabolism
  • Cell Survival / physiology
  • Cytoprotection / physiology
  • Disease Models, Animal
  • Hyperbaric Oxygenation*
  • In Situ Nick-End Labeling
  • Ischemic Preconditioning / methods*
  • Male
  • Nerve Degeneration / etiology
  • Nerve Degeneration / physiopathology
  • Nerve Degeneration / therapy*
  • Neuroanatomical Tract-Tracing Techniques
  • Optic Nerve / cytology
  • Optic Nerve / physiology
  • Optic Nerve Injuries / complications*
  • Rats
  • Rats, Sprague-Dawley
  • Retinal Degeneration / etiology
  • Retinal Degeneration / physiopathology
  • Retinal Degeneration / therapy*
  • Retinal Ganglion Cells / cytology
  • Retinal Ganglion Cells / physiology*
  • Staining and Labeling
  • Stilbamidines
  • Visual Pathways / cytology
  • Visual Pathways / injuries
  • Visual Pathways / physiology

Substances

  • 2-hydroxy-4,4'-diamidinostilbene, methanesulfonate salt
  • Stilbamidines
  • Caspase 3
  • Caspase 9