Circadian variation in enoxacin-induced convulsions in mice coadministered with fenbufen

Jpn J Pharmacol. 1997 Feb;73(2):175-7. doi: 10.1254/jjp.73.175.

Abstract

Susceptibility to enoxacin (80 mg/kg, p.o.)-induced convulsions was examined in mice coadministered with fenbufen (100 mg/kg, p.o.) over 24 hr at 3-hr intervals (light 7:00-19:00 hr). There was a marked circadian variation in the incidence of clonic and tonic convulsions and mortality. The susceptibility to enoxacin was higher around 15:00-18:00 hr and lower around 3:00-9:00 hr; the 50% clonic convulsive dose (CD50) at 9:00 and 15:00 hr was 95.0 and 56.5 mg/kg, respectively, its ratio being 1.64. Under these conditions, brain enoxacin level at 15:00 hr was increased 2.43-fold over that at 9:00 hr 30 min after enoxacin administration. Thus, the change of brain enoxacin may contribute to one of the causes of the above circadian variation.

MeSH terms

  • Animals
  • Anti-Infective Agents / blood
  • Anti-Infective Agents / pharmacokinetics
  • Anti-Infective Agents / toxicity*
  • Anti-Inflammatory Agents, Non-Steroidal / blood
  • Anti-Inflammatory Agents, Non-Steroidal / pharmacokinetics
  • Anti-Inflammatory Agents, Non-Steroidal / toxicity*
  • Brain / metabolism
  • Circadian Rhythm / physiology*
  • Drug Administration Schedule
  • Drug Interactions
  • Enoxacin / blood
  • Enoxacin / pharmacokinetics
  • Enoxacin / toxicity*
  • Male
  • Mice
  • Mice, Inbred Strains
  • Phenylbutyrates / blood
  • Phenylbutyrates / pharmacokinetics
  • Phenylbutyrates / toxicity*
  • Seizures / chemically induced*

Substances

  • Anti-Infective Agents
  • Anti-Inflammatory Agents, Non-Steroidal
  • Phenylbutyrates
  • Enoxacin
  • fenbufen