Pharmacological characterization of postjunctional alpha-adrenoceptors in human nasal mucosa

Am J Rhinol. 2005 Sep-Oct;19(5):495-502.

Abstract

Background: Functional alpha1- and alpha2-adrenoreceptor subtype pharmacology was characterized in an in vitro human nasal mucosa contractile bioassay.

Methods: Nasal mucosa was obtained from 49 donor patients and mucosal strips were placed in chambers filled with Krebs-Ringer solution and attached to isometric force transducers.

Results: Nonselective a-adrenoreceptor agonists epinephrine, norepinephrine, and oxymetazoline produced concentration-dependent contractions of isolated human nasal mucosa (pD2 = 5.2, 4.9, and 6.5, respectively). The alpha2-adrenoreceptor agonist BHT-920 (10 microM)-induced contractions were blocked by yohimbine (0.01-1 microM) and prazosin (0.01-1 microM) inhibited the contractile response to the alpha1-adrenoreceptor agonist phenylephrine (10 microM). Histological analysis showed that phenylephrine and BHT-920 differentially contracted the arteries and veins of human nasal mucosa, respectively.

Conclusion: Our results indicate that functional alpha1- and alpha2-adrenoceptors are present and functional in human nasal mucosa. The alpha2-adrenoceptors display a predominant role in contracting the veins and the alpha1-adrenoceptors appear to preferentially constrict the human nasal arteries.

MeSH terms

  • Adrenergic alpha-Agonists / pharmacology
  • Adrenergic alpha-Antagonists / pharmacology
  • Adult
  • Aged
  • Arteries / physiology
  • Epinephrine / pharmacology
  • Female
  • Humans
  • In Vitro Techniques
  • Male
  • Nasal Mucosa / blood supply*
  • Norepinephrine / pharmacology
  • Oxymetazoline / pharmacology
  • Prazosin / pharmacology
  • Receptors, Adrenergic, alpha / physiology*
  • Turbinates
  • Vasoconstriction / drug effects
  • Veins / physiology
  • Yohimbine / pharmacology

Substances

  • Adrenergic alpha-Agonists
  • Adrenergic alpha-Antagonists
  • Receptors, Adrenergic, alpha
  • Yohimbine
  • Oxymetazoline
  • Norepinephrine
  • Prazosin
  • Epinephrine