(S)-UH-301 antagonizes (R)-8-OH-DPAT-indiiced cardiovascular effects in the rat
Author:
Publisher
Elsevier BV
Subject
Pharmacology
Reference10 articles.
1. Björk, L., L.J. Cornfield, D.L. Nelson, S.-E. Hillver, N.-E. Anden, T. Lewander and U. Häcksell, Pharmacology of the novel 5-HT1A-receptor antagonist (S)-5-fluoro-8-hydroxy-2-(dipropylamino)tetralin, (SR3H-301: inhibition of (R)-S-OH DPAT-induced effects, J. Pharmacol. Exp. Ter. (in press).
2. Pentobarbital anaesthesia prevents the adrenaline-releasing effect of the 5-HT1A receptor agonist, 8-hydroxy-2-(di-n-propylamino)tetralin;Chaouloff;European J. Pharmacol.,1990
3. Cardiovascular effects of 5-HT1A receptor agonists injected into the dorsal raphe nucleus of conscious rats;Connor;European J. Pharmacol.,1990
4. Cardiovascular response to 8-hydroxy-2-(di-n-propylamino)tetralin (8-OH-DPAT) in the rat: site of action and pharmacological analysis;Fozard;J. Cardiovasc. Pharmacol.,1987
5. Acute administration of 8-hydroxy-2-(di-n-propylamino)tetralin (8-OH-DPAT), a selective 5-HT-receptor agonist, causes a biphasic blood pressure response and bradycardia in the normotensive Sprague-Dawley rat and in the spontaneously hypertensive rat;Gradin;J. Neural Transm.,1985
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