Aminophylline preferentially inhibits chloroethylclonidine-insensitive alpha-adrenoceptor-mediated contractions in rat aorta

Gen Pharmacol. 1993 Nov;24(6):1359-64. doi: 10.1016/0306-3623(93)90419-x.

Abstract

1. In rat thoracic aortae, contractions induced by methoxamine were inhibited by chloroethylclonidine, whereas oxymetazoline-induced contractions, which were more dependent on Ca(2+)-entry, were insensitive to chloroethylclonidine. 2. Aminophylline inhibited the contractions and 45Ca(2+)-uptake induced by both methoxamine and oxymetazoline. However, oxymetazoline-induced contractions were more sensitive to inhibition by aminophylline and D600. 3. Thus, the partial selectivity of aminophylline for the chloroethylclonidine-resistant, highly dependent on extracellular Ca2+, oxymetazoline-mediated responses may be explained by a preferential inhibition of agonist-induced Ca2+ entry as compared to inhibition of other transduction pathways.

MeSH terms

  • Adrenergic alpha-Agonists / pharmacology
  • Adrenergic alpha-Antagonists / pharmacology*
  • Aminophylline / pharmacology*
  • Animals
  • Aorta, Thoracic / drug effects*
  • Aorta, Thoracic / metabolism
  • Calcium / metabolism
  • Calcium Radioisotopes
  • Clonidine / analogs & derivatives*
  • Clonidine / pharmacology
  • Female
  • Gallopamil / pharmacology
  • In Vitro Techniques
  • Male
  • Methoxamine / antagonists & inhibitors
  • Methoxamine / pharmacology
  • Muscle Contraction / drug effects
  • Muscle, Smooth, Vascular / drug effects*
  • Muscle, Smooth, Vascular / metabolism
  • Oxymetazoline / antagonists & inhibitors
  • Oxymetazoline / pharmacology
  • Rats
  • Rats, Sprague-Dawley
  • Receptors, Adrenergic, alpha / drug effects*
  • Receptors, Adrenergic, alpha / metabolism

Substances

  • Adrenergic alpha-Agonists
  • Adrenergic alpha-Antagonists
  • Calcium Radioisotopes
  • Receptors, Adrenergic, alpha
  • Aminophylline
  • Gallopamil
  • chlorethylclonidine
  • Oxymetazoline
  • Methoxamine
  • Clonidine
  • Calcium