Nitric oxide synthase gene expression in injured spinal cord tissue

Chin Med J (Engl). 2002 May;115(5):740-2.

Abstract

Objective: To investigate gene expression of three nitric oxide synthase isozymes in injured spinal cord tissue.

Methods: Thirty-six adult SD rats were randomly divided into six groups: a normal group and five injury groups, with six per each group. Animals in the injury groups were sacrificed at 2, 6, 12, 24, 48 h after injury. A compression injury model on the spinal cord was made according to Nystrom B et al and gene expression of the three NOS isozymes were examined by reverse transcription polymerase chain reaction (RT-PCR).

Results: Gene expression of nNOS and eNOS were detectable in the normal group and were up-regulated quickly after injury, reaching a maximum at 6 h: (0.633 +/- 0.012) and (1.236 +/- 0.207). Gene expression of iNOS was detectable only in the injury groups and it was gradually up-regulated after injury, reaching a maximum at 24 h: (1.043 +/- 0.049).

Conclusion: Injury to the spinal cord leads to early up-regulation of cNOS and late up-regulation of iNOS. Different NOS isozymes may play different roles in secondary spinal cord injury.

MeSH terms

  • Animals
  • Female
  • Gene Expression Regulation, Enzymologic
  • Male
  • Nitric Oxide Synthase / genetics*
  • Nitric Oxide Synthase Type I
  • Nitric Oxide Synthase Type II
  • Nitric Oxide Synthase Type III
  • RNA / genetics
  • RNA / metabolism
  • Rats
  • Rats, Sprague-Dawley
  • Reverse Transcriptase Polymerase Chain Reaction
  • Spinal Cord / enzymology
  • Spinal Cord / pathology
  • Spinal Cord Injuries / enzymology*
  • Spinal Cord Injuries / genetics

Substances

  • RNA
  • Nitric Oxide Synthase
  • Nitric Oxide Synthase Type I
  • Nitric Oxide Synthase Type II
  • Nitric Oxide Synthase Type III
  • Nos1 protein, rat
  • Nos2 protein, rat
  • Nos3 protein, rat