Cyclooxygenase inhibitors attenuate augmented glutamate release in organum vasculosum laminae terminalis and fever induced by staphylococcal enterotoxin A

J Pharmacol Sci. 2004 Feb;94(2):192-6. doi: 10.1254/jphs.94.192.

Abstract

Both the hyperthermia and augmented glutamate release in the organum vasculosum laminae terminalis (OVLT) after an intravenous dose (30 ng/kg) of staphylococcal enterotoxin A (SEA) were significantly reduced by pretreatment with intravenous administration of cyclooxygenase inhibitors such as aspirin (1 - 10 mg/kg), sodium salicylate (1 - 10 mg/kg), or diclofenac (10 mg/kg). Intra-OVLT administration of 50 - 200 microg in 1.0 microl of either aspirin or sodium salicylate 60 min before or 120 min after an intra-OVLT dose (50 microg in 1.0 microl) of glutamate also significantly suppressed the glutamate-induced hyperthermia. These findings suggest that inhibition of cyclooxygenase receptor mechanisms suppresses SEA fever by inhibition of glutamate release in the OVLT of rabbit brain.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cyclooxygenase Inhibitors / pharmacology*
  • Enterotoxins / toxicity*
  • Fever / chemically induced
  • Fever / enzymology*
  • Fever / metabolism
  • Fever / microbiology
  • Glutamic Acid / metabolism*
  • Hypothalamus / drug effects*
  • Hypothalamus / enzymology*
  • Hypothalamus / metabolism
  • Male
  • Rabbits

Substances

  • Cyclooxygenase Inhibitors
  • Enterotoxins
  • enterotoxin A, Staphylococcal
  • Glutamic Acid