| Literature DB >> 5726781 |
A Barnett, S Symchowicz, R I Taber.
Abstract
1. Cocaine did not antagonize the tyramine-induced contractile response of the isolated rat vas deferens at the same concentrations which markedly potentiated the contractile response to noradrenaline.2. Imipramine and amitriptyline non-competitively antagonized the contractile response to tyramine but did not potentiate noradrenaline. Desmethylimipramine produced both potentiation of noradrenaline and antagonism of tyramine.3. Dexchlorpheniramine non-competitively antagonized the contractile response to tyramine. It also produced an atypical potentiation of noradrenaline in which lower concentrations of noradrenaline were potentiated to a greater extent than higher ones.4. Imipramine inhibited the in vitro uptake of noradrenaline-(3)H in rat vas deferens as did cocaine, desmethylimipramine and dexchlorpheniramine. These results suggest that the alpha-adrenergic blocking property of imipramine masks the potentiation of noradrenaline by uptake inhibition.5. Evidence is also presented which suggests that alpha-adrenergic blockade of released noradrenaline may be the major mechanism for tyramine inhibition by imipramine-like drugs. This may explain why cocaine, which has no real alpha blocking action, is ineffective against tyramine.Entities:
Mesh:
Substances:
Year: 1968 PMID: 5726781 PMCID: PMC1703532 DOI: 10.1111/j.1476-5381.1968.tb08476.x
Source DB: PubMed Journal: Br J Pharmacol ISSN: 0007-1188 Impact factor: 8.739