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The neuroprotective effect of a new serotonin receptor agonist, BAY X3702, upon focal ischemic brain damage caused by acute subdural hematoma in the rat.

Abstract
We tested the neuroprotective effect of a novel, high affinity serotonin (5-HT1A) agonist, BAY X3702, in a rat model of acute subdural hematoma (ASDH). Animals were treated with 0.01 mg/kg (n=8), 0.003 mg/kg (n=8) BAY X3702 or vehicle (n=4) 15 min before (i.v.) and after (continuous infusion) injection of 400 microl of autologous blood into the subdural space. The ischemic brain damage at 4 h after ASDH was 59.01+/-39 and 60.8+/-49 mm(3) for the low- and high-dose BAY X3702 group, respectively, which was significantly smaller compared to the vehicle-treated ASDH group (106.2+/-33 mm(3)). The result indicates that this novel, high affinity 5-HT(1A) agonist, BAY X3702, is neuroprotective in this model.
AuthorsB Alessandri, E Tsuchida, R M Bullock
JournalBrain research (Brain Res) Vol. 845 Issue 2 Pg. 232-5 (Oct 23 1999) ISSN: 0006-8993 [Print] Netherlands
PMID10536203 (Publication Type: Journal Article, Research Support, U.S. Gov't, P.H.S.)
Chemical References
  • Benzopyrans
  • Neuroprotective Agents
  • Receptors, Serotonin
  • Receptors, Serotonin, 5-HT1
  • Serotonin Receptor Agonists
  • Thiazoles
  • repinotan hydrochloride
Topics
  • Animals
  • Benzopyrans (pharmacology)
  • Brain Ischemia (drug therapy, etiology)
  • Dose-Response Relationship, Drug
  • Hematoma, Subdural, Acute (complications)
  • Male
  • Neuroprotective Agents (pharmacology)
  • Rats
  • Rats, Sprague-Dawley
  • Receptors, Serotonin (physiology)
  • Receptors, Serotonin, 5-HT1
  • Serotonin Receptor Agonists (pharmacology)
  • Thiazoles (pharmacology)

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