Characterization of hydroxyl radical generation in the striatum of free-moving rats due to carbon monoxide poisoning, as determined by in vivo microdialysis

Brain Res. 2004 Aug 6;1016(2):281-4. doi: 10.1016/j.brainres.2004.05.047.

Abstract

Carbon monoxide (CO) poisoning caused by CO exposure at 3000 ppm for 40 min resulted in stimulation of hydroxyl radical (*OH) generation (estimated by measuring 2,3-dihydroxybenzoic acid (2,3-DHBA) production from salicylic acid) in the striatum of free-moving rats, as determined by means of brain microdialysis. Pretreatment with a voltage-dependent Na+ channel blocker, tetrodotoxin (TTX), lowered the basal level of 2,3-DHBA and strongly suppressed the increase in 2,3-DHBA induced by CO poisoning. CO poisoning significantly, though only slightly, increased extracellular glutamate in the striatum, and glutamate (Glu) receptor antagonists, such as MK-801 (dizocilpine) and NBQX, failed to suppress the CO-induced increase in 2,3-DHBA. These findings suggest that CO poisoning may induce Na+ influx via the voltage-dependent Na+ channels, resulting in stimulation of *OH generation in rat striatum. This effect may be independent of Glu receptor activation by increased extracellular Glu.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Carbon Monoxide Poisoning / metabolism*
  • Corpus Striatum / drug effects*
  • Corpus Striatum / metabolism
  • Dizocilpine Maleate / pharmacology
  • Excitatory Amino Acid Antagonists / pharmacology
  • Glutamic Acid / metabolism
  • Hydroxybenzoates
  • Hydroxyl Radical / metabolism*
  • Male
  • Microdialysis / methods*
  • Quinoxalines / pharmacology
  • Rats
  • Rats, Sprague-Dawley
  • Tetrodotoxin / pharmacology
  • Wakefulness / drug effects
  • Wakefulness / physiology

Substances

  • Excitatory Amino Acid Antagonists
  • Hydroxybenzoates
  • Quinoxalines
  • 2,3-dioxo-6-nitro-7-sulfamoylbenzo(f)quinoxaline
  • Hydroxyl Radical
  • Glutamic Acid
  • Tetrodotoxin
  • Dizocilpine Maleate
  • 2,3-dihydroxybenzoic acid