Abstract |
The cardiovascular effects of RDS-127 [2-di-n-propylamino-4,7-dimethoxyindane] were examined in normotensive, anaesthetized rats. RDS-127 given i.v. (12.5-125 micrograms kg-1) produced dose-dependent bradycardia. The bradycardic effect was 20.5 times more potent when the drug was administered intracerebroventricularly (i.c.v.) than when given i.v. RDS-127 produced a slight, but significant hypotension. Haloperidol given i.c.v. or i.v. reversed these bradycardic and hypotensive actions, whereas phentolamine was ineffective. Methylatropine partially reduced the bradycardic effect. These results suggest that RDS-127 activates central DA receptors to produce hypotension and bradycardia in rats.
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Authors | S P Arnerić, J P Long |
Journal | The Journal of pharmacy and pharmacology
(J Pharm Pharmacol)
Vol. 36
Issue 5
Pg. 318-21
(May 1984)
ISSN: 0022-3573 [Print] England |
PMID | 6145768
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't, Research Support, U.S. Gov't, P.H.S.)
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Chemical References |
- Atropine Derivatives
- Indans
- Indenes
- Receptors, Dopamine
- methylatropine
- 2-N,N-di-n-propylamino-4,7-dimethoxyindan
- Haloperidol
- Phentolamine
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Topics |
- Animals
- Atropine Derivatives
(pharmacology)
- Blood Pressure
(drug effects)
- Brain
(drug effects)
- Drug Interactions
- Haloperidol
(pharmacology)
- Heart Rate
(drug effects)
- Hemodynamics
(drug effects)
- Indans
(administration & dosage, pharmacology)
- Indenes
(pharmacology)
- Injections, Intravenous
- Injections, Intraventricular
- Male
- Phentolamine
(pharmacology)
- Rats
- Rats, Inbred Strains
- Receptors, Dopamine
(drug effects)
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