Abstract |
The antiemetic effects of six serotonergic 5-HT1A-receptor agonists, 8-hydroxy-2-(di-n-propylamino)tetrarin (8-OH-DPAT), 4-(4-[4-(2-pyrimidinyl)piperazin-1-yl]butyl)-2,3,4,5- tetrahydro-1,4-benzoxazepine-3,5-dione ( SUN8399), buspirone, gepirone, ipsapirone and tandospirone, against motion sickness were investigated in Suncus murinus. Subcutaneous injection of all six agonists completely and dose-dependently suppressed motion-induced emesis. Pretreatment with 8-OH-DPAT or SUN8399 dose-dependently inhibited emesis elicited by nicotine (4.0 mg/kg, s.c.), veratrine (0.7 mg/kg, s.c.), cisplatin (20 mg/kg, i.p.) and copper sulfate (40 mg/kg, p.o.). These results suggest that serotonergic 5-HT1A-receptor agonists are effective as anti- motion sickness drugs, and these drugs may block a common mechanism(s) for the emetic reflex of the suncus because the antiemetic effects of the 5-HT1A-receptor agonists were exerted irrespective of the stimulus.
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Authors | F Okada, Y Torii, H Saito, N Matsuki |
Journal | Japanese journal of pharmacology
(Jpn J Pharmacol)
Vol. 64
Issue 2
Pg. 109-14
(Feb 1994)
ISSN: 0021-5198 [Print] Japan |
PMID | 8028227
(Publication Type: Journal Article)
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Chemical References |
- Antiemetics
- Oxazepines
- Serotonin Receptor Agonists
- SUN 8399
- 8-Hydroxy-2-(di-n-propylamino)tetralin
- Buspirone
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Topics |
- 8-Hydroxy-2-(di-n-propylamino)tetralin
(pharmacology)
- Animals
- Antiemetics
(pharmacology)
- Buspirone
(pharmacology)
- Dose-Response Relationship, Drug
- Male
- Motion Sickness
(prevention & control)
- Oxazepines
(pharmacology)
- Serotonin Receptor Agonists
(pharmacology)
- Shrews
(physiology)
- Vomiting
(chemically induced, prevention & control)
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