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.
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Authors | B Alessandri, E Tsuchida, R M Bullock |
Journal | Brain research
(Brain Res)
Vol. 845
Issue 2
Pg. 232-5
(Oct 23 1999)
ISSN: 0006-8993 [Print] Netherlands |
PMID | 10536203
(Publication Type: Journal Article, Research Support, U.S. Gov't, P.H.S.)
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Chemical References |
- Benzopyrans
- Neuroprotective Agents
- Receptors, Serotonin
- Receptors, Serotonin, 5-HT1
- Serotonin Receptor Agonists
- Thiazoles
- repinotan hydrochloride
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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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