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Dexanabinol; a novel neuroprotective drug in experimental focal cerebral ischemia.

Abstract
The permanent middle cerebral artery occlusion (PMCAO) model was used to investigate the cerebroprotective effects of the synthetic cannabinoid, dexanabinol (HU-211). Dexanabinol is a noncompetitive N-methyl-D-aspartate antagonist, with antioxidant and anti-TNFalpha properties. Twenty hypertensive rats were subjected to PMCAO. Eight were given 4 mg/kg dexanabinol, i.v., 1 h after PMCAO, eight received vehicle and four were not injected Five rats underwent sham surgery. Infarct volumes were assessed, as well as TNFalpha concentrations and NOS activity in brain homogenates. Dexanabinol significantly decreased infarct volumes. It also significantly lowered TNFalpha levels in the ipsilateral hemisphere although not to the level of sham operated rats. No effect could be demonstrated on NOS activity. In conclusion, dexanabinol may be a pluripotent cerebroprotective agent.
AuthorsR R Leker, E Shohami, O Abramsky, H Ovadia
JournalJournal of the neurological sciences (J Neurol Sci) Vol. 162 Issue 2 Pg. 114-9 (Jan 15 1999) ISSN: 0022-510X [Print] Netherlands
PMID10202976 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Excitatory Amino Acid Antagonists
  • Neuroprotective Agents
  • Tumor Necrosis Factor-alpha
  • Dronabinol
  • Nitric Oxide Synthase
  • HU 211
Topics
  • Animals
  • Arterial Occlusive Diseases (complications, drug therapy)
  • Disease Models, Animal
  • Dronabinol (analogs & derivatives, therapeutic use)
  • Drug Evaluation, Preclinical
  • Excitatory Amino Acid Antagonists (therapeutic use)
  • Hypertension (complications)
  • Ischemic Attack, Transient (prevention & control)
  • Male
  • Neuroprotective Agents (therapeutic use)
  • Nitric Oxide Synthase (metabolism)
  • Rats
  • Rats, Inbred SHR
  • Tumor Necrosis Factor-alpha (metabolism)

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