Hyperbaric oxygen preconditioning induces tolerance against oxidative injury and oxygen-glucose deprivation by up-regulating heat shock protein 32 in rat spinal neurons

PLoS One. 2014 Jan 17;9(1):e85967. doi: 10.1371/journal.pone.0085967. eCollection 2014.

Abstract

Objective: Hyperbaric oxygen (HBO) preconditioning (HBO-PC) has been testified to have protective effects on spinal cord injury (SCI). However, the mechanisms remain enigmatic. The present study aimed to explore the effects of HBO-PC on primary rat spinal neurons against oxidative injury and oxygen-glucose deprivation (OGD) and the relationship with heat shock proteins (HSPs).

Methods: Primary rat spinal neurons after 7 days of culture were used in this study. HSPs were detected in rat spinal neurons following a single exposure to HBO at different time points by Western blot. Using lactate dehydrogenase release assay and cell counting kit-8 assay, the injuries induced by hydrogen peroxide (H2O2) insult or OGD were determined and compared among neurons treated with HBO-PC with or without HSP inhibitors.

Results: The results of Western blot showed that HSP27, HSP70 and HSP90 have a slight but not significant increase in primary neurons following HBO exposure. However, HSP32 expression significantly increased and reached highest at 12 h following HBO exposure. HBO-PC significantly increased the cell viability and decreased the medium lactate dehydrogenase content in cultures treated with H2O2 or OGD. Pretreatment with zinc protoporphyrin IX, a specific inhibitor of HSP32, significantly blocked the protective effects of HBO-PC.

Conclusions: These results suggest that HBO-PC could protect rat spinal neurons in vitro against oxidative injury and OGD mostly by up-regulating of HSP32 expression.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cells, Cultured
  • Glucose / deficiency*
  • Heme Oxygenase (Decyclizing) / metabolism*
  • Hyperbaric Oxygenation*
  • Hypoxia / pathology
  • Neurons / drug effects
  • Neurons / metabolism*
  • Oxidative Stress / drug effects*
  • Oxygen / pharmacology*
  • Rats
  • Spinal Cord Injuries / metabolism
  • Spinal Cord Injuries / pathology
  • Spine / drug effects
  • Spine / pathology*
  • Time Factors
  • Up-Regulation / drug effects*

Substances

  • Heme Oxygenase (Decyclizing)
  • Hmox1 protein, rat
  • Glucose
  • Oxygen

Grants and funding

This work was supported by the National Natural Science Foundation of China, No. 81171873. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.