The effects of drugs inhibiting catecholamine uptake on tyramine and noradrenaline-induced contractions of the isolated rat vas deferens

Br J Pharmacol. 1968 Nov;34(3):484-92. doi: 10.1111/j.1476-5381.1968.tb08476.x.

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.

MeSH terms

  • Animals
  • Catecholamines / metabolism
  • Cocaine / pharmacology
  • Drug Antagonism*
  • Imipramine / pharmacology
  • Male
  • Muscle Contraction / drug effects*
  • Norepinephrine / pharmacology
  • Rats
  • Tritium
  • Tyramine / pharmacology
  • Vas Deferens / drug effects*

Substances

  • Catecholamines
  • Tritium
  • Cocaine
  • Imipramine
  • Norepinephrine
  • Tyramine