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Effects of a novel calcium antagonist, KB-2796, on neurologic outcome and size of experimental cerebral infarction in rats.

Abstract
Effects of a novel calcium 2+ antagonist, KB-2796, on neurologic outcome and size of infarction were studied in the rat model of focal cerebral ischemia. Neurologic deficits were examined from 1 to 24 hours after occlusion of the middle cerebral artery and size of infarction was measured at 24 hours postocclusion. When KB-2796 (10 mg/kg, IP) was given immediately after, or 1 hour after, middle cerebral artery occlusion, marked improvement in neurologic score was seen 1 to 3 hours postocclusion. When given immediately after middle cerebral artery occlusion, size of infarction was also markedly smaller when compared with the control rat. The present study suggests that the calcium 2+ antagonist KB-2796 has brain-protective effects against ischemia even with its administration after induction of ischemia.
AuthorsK Harada, A Shiino, M Matsuda, J Handa
JournalSurgical neurology (Surg Neurol) Vol. 32 Issue 1 Pg. 16-20 (Jul 1989) ISSN: 0090-3019 [Print] United States
PMID2734684 (Publication Type: Journal Article)
Chemical References
  • Calcium Channel Blockers
  • Piperazines
  • lomerizine
Topics
  • Animals
  • Brain (pathology)
  • Calcium Channel Blockers (therapeutic use)
  • Cerebral Infarction (drug therapy, pathology, physiopathology)
  • Male
  • Nervous System (physiopathology)
  • Piperazines (therapeutic use)
  • Rats
  • Rats, Inbred Strains
  • Time Factors

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