Characterization of the postjunctional alpha 2C-adrenoceptor mediating vasoconstriction to UK14304 in porcine pulmonary veins

Br J Pharmacol. 2007 May;151(2):186-94. doi: 10.1038/sj.bjp.0707221. Epub 2007 Mar 20.

Abstract

Background and purpose: In terms of postjunctional alpha(2)-adrenoceptors in the pulmonary circulation, no evidence is available with regard to the receptor subtypes mediating vasoconstriction. Therefore, we characterized the alpha(2)-adrenoceptor subtypes mediating contraction in isolated porcine pulmonary veins.

Experimental approach: alpha-adrenoceptor-mediated vasoconstriction was studied using a tissue bath protocol. mRNA profile and relative quantification of alpha(2)-adrenoceptor subtypes were determined in porcine pulmonary veins using reverse-transcriptase polymerase chain reaction (RT-PCR) and real-time PCR.

Key results: In porcine pulmonary veins, noradrenaline, phenylephrine (alpha(1)-adrenoceptor agonist), UK14304 and clonidine (alpha(2)-adrenoceptor agonists) caused concentration-dependent contractions. The rank order of agonist potency was: NA approximately UK14304 approximately clonidine > phenylephrine. UK14304 responses were antagonised by MK912 (noncompetitive antagonist parameter pD'(2): 10.1), rauwolscine (pK(B): 9.5), yohimbine (pK(B): 9.1), WB4101 (pK(B): 8.7), ARC239 (pK(B): 7.5), prazosin (pK(B): 7.1) and BRL44408 (pK(B): 7.0). Antagonist potencies fitted best with radioligand binding data (pK(i)) at the human recombinant alpha(2C)-adrenoceptor (r(2)=0.96, P=0.0001). Correlation with alpha(2B)-adrenoceptors was lower (r(2)=0.74, P>0.01) and no correlation was obtained with alpha(2A)-adrenoceptors. Moreover, RT-PCR studies in porcine pulmonary veins showed mRNA signals for alpha(2A)- and alpha(2C)-adrenoceptors, but not for alpha(2B)-adrenoceptors, whilst real-time PCR studies indicated a prominent expression of alpha(2C)-adrenoceptor mRNA.

Conclusions and implications: Postjunctional alpha(2C)-adrenoceptors mediated contraction in porcine pulmonary veins. alpha(1)-Adrenoceptors also seem to be present in this tissue. Since alpha(2)-adrenoceptor responsiveness is increased when pulmonary vascular tone is elevated, alpha(2C)-adrenoceptor antagonists may be beneficial in diseases such as pulmonary hypertension or congestive heart failure.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adrenergic alpha-Agonists / pharmacology
  • Adrenergic alpha-Antagonists / pharmacology
  • Animals
  • Brimonidine Tartrate
  • Clonidine / pharmacology
  • Dioxanes / pharmacology
  • Dose-Response Relationship, Drug
  • Gene Expression / drug effects
  • Imidazoles / pharmacology
  • In Vitro Techniques
  • Indoles / pharmacology
  • Isoindoles
  • Isoquinolines / pharmacology
  • Neuromuscular Junction / metabolism
  • Norepinephrine / pharmacology
  • Piperazines / pharmacology
  • Prazosin / pharmacology
  • Pulmonary Veins / drug effects*
  • Pulmonary Veins / innervation
  • Pulmonary Veins / physiology
  • Quinolizines / pharmacology
  • Quinoxalines / pharmacology*
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Receptors, Adrenergic, alpha-1 / genetics
  • Receptors, Adrenergic, alpha-1 / physiology
  • Receptors, Adrenergic, alpha-2 / genetics
  • Receptors, Adrenergic, alpha-2 / physiology*
  • Reverse Transcriptase Polymerase Chain Reaction
  • Swine
  • Vasoconstriction / drug effects*
  • Yohimbine / pharmacology

Substances

  • ADRA2A protein, human
  • ADRA2C protein, human
  • Adrenergic alpha-Agonists
  • Adrenergic alpha-Antagonists
  • Dioxanes
  • Imidazoles
  • Indoles
  • Isoindoles
  • Isoquinolines
  • Piperazines
  • Quinolizines
  • Quinoxalines
  • RNA, Messenger
  • Receptors, Adrenergic, alpha-1
  • Receptors, Adrenergic, alpha-2
  • L 657743
  • Yohimbine
  • Brimonidine Tartrate
  • (2-(2',6'-dimethoxy)phenoxyethylamino)methylbenzo-1,4-dioxane
  • AR-C239
  • Clonidine
  • Norepinephrine
  • Prazosin
  • BRL 44408