The effects of dizocilpine (MK-801), phencyclidine, and nimodipine on infarct size 48 h after middle cerebral artery occlusion in the rat

Brain Res. 1991 Jun 28;552(2):338-42. doi: 10.1016/0006-8993(91)90101-z.

Abstract

The effects of the calcium channel blocker nimodipine and the non-competitive NMDA-antagonists MK-801 and phencyclidine (PCP) on infarct size 48 h after occlusion of the middle cerebral artery (MCA-O) were evaluated in the rat. Nimodipine was given at a dose of 0.3 mg/kg s.c. 30 min prior and 8, 16, and 24 h after MCA-O. MK-801 (1 mg/kg i.p. or 10 mg/kg i.p.) or PCP (0.3, 1.0, 3.0, 10, or 30 mg/kg i.p.) were administered 30 min prior to ischemia. In additional experiments 30 mg/kg PCP was given 1, 3, or 5 h post ischemia. Nimodipine and 1 mg/kg MK-801 reduced cortical infarct volumes significantly by 50% and 55%, respectively, while cortical infarct size fell by 32% and total infarct volume was not altered significantly after administration of 10 mg/kg MK-801. Pretreatment with 10 or 30 mg/kg PCP reduced cortical infarction by 47-53% and total infarct volumes by 39-42%. Posttreatment with PCP was effective if started at 1 or 3 h post ischemia.

MeSH terms

  • Animals
  • Blood Glucose / metabolism
  • Blood Pressure / drug effects
  • Carbon Dioxide / blood
  • Cerebral Arteries / physiopathology*
  • Cerebral Infarction / pathology
  • Cerebral Infarction / physiopathology*
  • Dizocilpine Maleate / pharmacology*
  • Ischemic Attack, Transient / physiopathology*
  • Nimodipine / pharmacology*
  • Oxygen / blood
  • Partial Pressure
  • Phencyclidine / pharmacology*
  • Rats
  • Rats, Inbred F344
  • Time Factors

Substances

  • Blood Glucose
  • Carbon Dioxide
  • Nimodipine
  • Dizocilpine Maleate
  • Phencyclidine
  • Oxygen