Pharmacological characterization of alpha1-adrenoceptor in mouse iliac artery

Eur J Pharmacol. 2002 Dec 5;456(1-3):77-9. doi: 10.1016/s0014-2999(02)02649-3.

Abstract

Subtypes of alpha(1)-adrenoceptor-mediated contraction to noradrenaline in the mouse iliac artery were determined (pharmaco-mechanically). Prazosin, 2-[2,6-dimethoxyphenoxyethyl]aminomethyl-1,4-benzodioxane hydrochloride (WB 4101) and 5-methylurapidil shifted the concentration-response curve for noradrenaline to the right, giving the pA(2) values of 9.30, 9.55 and 8.71, respectively. 8-[2-[4-(2-Methoxyphenyl)-1-piperazinyl]-ethyl]-8-azaspiro[4,5]decane-7,9-dione dihydrochloride (BMY 7378) shifted the concentration-response curve for noradrenaline to the right and the pA(2) value was 6.62. These results indicate that the contractile response to noradrenaline in the mouse iliac artery is predominantly mediated by the alpha(1A) -adrenoceptor subtype.

MeSH terms

  • Adrenergic alpha-1 Receptor Agonists
  • Adrenergic alpha-1 Receptor Antagonists
  • Adrenergic alpha-Antagonists / pharmacology
  • Animals
  • Dioxanes / pharmacology
  • Dose-Response Relationship, Drug
  • Iliac Artery / drug effects*
  • Iliac Artery / physiology
  • In Vitro Techniques
  • Male
  • Mice
  • Norepinephrine / pharmacology
  • Piperazines / pharmacology
  • Prazosin / pharmacology
  • Receptors, Adrenergic, alpha-1 / physiology*
  • Vasoconstriction / drug effects*

Substances

  • Adrenergic alpha-1 Receptor Agonists
  • Adrenergic alpha-1 Receptor Antagonists
  • Adrenergic alpha-Antagonists
  • Dioxanes
  • Piperazines
  • Receptors, Adrenergic, alpha-1
  • 5-methylurapidil
  • (2-(2',6'-dimethoxy)phenoxyethylamino)methylbenzo-1,4-dioxane
  • BMY 7378
  • Norepinephrine
  • Prazosin