All preconditioning-related G protein-coupled receptors can be demonstrated in the rabbit cardiomyocyte

J Cardiovasc Pharmacol Ther. 2012 Jun;17(2):190-8. doi: 10.1177/1074248411416815. Epub 2011 Aug 9.

Abstract

G protein-coupled receptors for adenosine (A(1), A(3), A(2A), and A(2B)), bradykinin (B(1)) and opioids (δ) are all involved in the mechanism of ischemic preconditioning. Although the heart is comprised of many tissue types, it has been assumed that preconditioning's protective signaling occurs in the cardiomyocyte. We critically tested that hypothesis by testing for the presence of each of these receptors in isolated adult rabbit ventricular myocytes that had been transfected with cyclic nucleotide-gated (CNG) ion channels. Because subsarcolemmal cyclic adenosine monophosphate (cAMP) opens the CNG channels, we could monitor cAMP levels within a single cardiomyocyte by measuring channel current with a patch pipette. The presence of a receptor would be confirmed if we could alter cAMP in the cell with a selective agonist to the receptor being studied. Superfusion with the β-adrenergic G(s)-coupled receptor agonist isoproterenol (50 nmol/L) transiently increased cAMP levels and, therefore, channel current. Pretreatment with selective agonists to A(1) or A(3) adenosine receptors (ARs) that are G(i)-coupled markedly attenuated the response to isoproterenol, indicating inhibition of adenylyl cyclase by increased G(i) activity. Agonists to bradykinin or δ-opioid receptors also attenuated isoproterenol's response. A(2A)AR and A(2B)AR are G(s)-coupled. The A(2A)AR-selective agonist CGS21680 increased current through CNG channels but only in the presence of phosphodiesterase (PDE) inhibitors, indicating low surface receptor activity and high intracellular PDE activity. As we previously reported, BAY 60-6583, an A(2B)AR-selective agonist which mimics preconditioning's protection in rabbit heart, neither increased nor decreased membrane current in transfected cardiomyocytes, suggesting the absence or a markedly limited number of A(2B)AR in the sarcolemma. However, reverse transcription polymerase chain reaction (RT-PCR) of purified cardiomyocytes yielded an A(2B)AR band, implying that rabbit cardiomyocytes do indeed express A(2B)AR. These data reveal that all receptors reported to be involved in ischemic preconditioning do exist on or within the cardiomyocyte.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • Cyclic AMP / metabolism
  • Cyclic Nucleotide-Gated Cation Channels / metabolism
  • Female
  • Heart Ventricles / cytology
  • Ischemic Preconditioning / methods
  • Isoproterenol / pharmacology
  • Male
  • Myocytes, Cardiac / metabolism*
  • Purinergic P1 Receptor Agonists / pharmacology
  • Rabbits
  • Receptor, Bradykinin B1 / agonists
  • Receptor, Bradykinin B1 / metabolism*
  • Receptors, Opioid, delta / agonists
  • Receptors, Opioid, delta / metabolism*
  • Receptors, Purinergic P1 / drug effects
  • Receptors, Purinergic P1 / metabolism*
  • Reverse Transcriptase Polymerase Chain Reaction
  • Sarcolemma / metabolism
  • Transfection

Substances

  • Cyclic Nucleotide-Gated Cation Channels
  • Purinergic P1 Receptor Agonists
  • Receptor, Bradykinin B1
  • Receptors, Opioid, delta
  • Receptors, Purinergic P1
  • Cyclic AMP
  • Isoproterenol