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Indian J Physiol Pharmacol ; 1986 Oct-Dec; 30(4): 307-12
Article in English | IMSEAR | ID: sea-108020

ABSTRACT

Tranylcypromine (TCP) pretreatment was found to accelerate the tremorogenic activity of tremorine in rats. Conversely, reserpinization delayed the onset of induction of tremors, and a significant diminution in their intensity was observed in these rats. A comparative study of the antitremor activity of beta-adrenoceptor antagonists against this tremor-model showed that butoxamine (beta 2-antagonist) and propranolol (nonselective antagonist) were able to afford a rapid and powerful protection, whereas a weaker and delayed effect was observed in rats treated with the beta 1-antagonist, acebutolol. Furthermore, the antitremor activity of butoxamine and propranolol but not that of acebutolol was found to be potentiated and diminished in rats pretreated with reserpine and TCP, respectively. It was inferred that beta 2-receptor modulated the tremorogenic activity of tremorine, and that inhibition by propranolol or butoxamine of this subtype beta-adrenoceptor resulted in rapid and powerful suppression of tremors, and that the antiadrenergic activity of acebutolol was unlikely to have a role in its antitremor effect.


Subject(s)
Adrenergic beta-Antagonists/pharmacology , Animals , Dose-Response Relationship, Drug , Female , Male , Rats , Receptors, Muscarinic/drug effects , Reserpine/pharmacology , Sympathetic Nervous System/physiology , Tranylcypromine/pharmacology , Tremor/chemically induced , Tremorine/antagonists & inhibitors
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