Abstract |
The effects of some noradrenergic agents, phenobarbitone, diazepam and phenytoin on seizures produced by propranolol were investigated in mice. Isoprenaline and DL-threo-3,4-dihydroxyphenylserine (DOPS) effectively antagonized the seizures elicited by propranolol. Pargyline and imipramine significantly attenuated propranolol-induced seizures and also significantly potentiated the protecting effect of DOPS against the seizures. alpha-Methyl-p-tyrosine, disulfiram and reserpine significantly potentiated propranolol-elicited seizures. However, DOPS significantly antagonized the seizure-potentiating effects of alpha-methyl-p-tyrosine, disulfiram and reserpine. Phenylephrine, clonidine, prazosin, idazoxan, phenobarbitone, diazepam and phenytoin did not significantly alter propranolol-induced seizures. These results suggest that propranolol-induced seizures in mice may involve a noradrenergic mechanism mediated via central beta- adrenoceptors.
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Authors | G J Amabeoku, J A Syce |
Journal | Cellular and molecular life sciences : CMLS
(Cell Mol Life Sci)
Vol. 53
Issue 8
Pg. 646-51
(Aug 1997)
ISSN: 1420-682X [Print] Switzerland |
PMID | 9351467
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Adrenergic Uptake Inhibitors
- Adrenergic alpha-Agonists
- Adrenergic beta-Agonists
- alpha-Methyltyrosine
- Reserpine
- Pargyline
- Propranolol
- Droxidopa
- Isoproterenol
- Imipramine
- Disulfiram
- Norepinephrine
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Topics |
- Adrenergic Uptake Inhibitors
(pharmacology)
- Adrenergic alpha-Agonists
(pharmacology)
- Adrenergic beta-Agonists
(pharmacology)
- Animals
- Disulfiram
(pharmacology)
- Droxidopa
(pharmacology)
- Drug Synergism
- Female
- Imipramine
(pharmacology)
- Isoproterenol
(pharmacology)
- Male
- Mice
- Norepinephrine
(physiology)
- Pargyline
(pharmacology)
- Propranolol
- Reserpine
(pharmacology)
- Seizures
(chemically induced)
- alpha-Methyltyrosine
(pharmacology)
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