Adenosine stimulates nitric oxide synthesis in rat cardiac myocytes

Am J Physiol. 1997 Jul;273(1 Pt 2):H59-65. doi: 10.1152/ajpheart.1997.273.1.H59.

Abstract

We investigated the effects of adenosine on nitric oxide (NO) synthesis by measuring the production of nitrite, a stable metabolite of NO, in cultured neonatal rat cardiac myocytes. Incubation of cultures with interleukin-1 beta (10 ng/ml) for 24 h caused a significant increase in nitrite production. The interleukin-1 beta-induced nitrite production by cardiac myocytes was significantly increased by adenosine or its stable analog 2-chloroadenosine in a dose-dependent manner (10(-7)-10(-4) M). The adenosine A2-receptor antagonist KF-17837 (10(-6) M), but not the A1-receptor antagonist 8-cyclopentyl-1, 3-dipropylxanthine (10(-6) M), significantly inhibited 2-chloroadenosine-mediated nitrite production. The 2-chloroadenosine-induced nitrite production by interleukin-1 beta-stimulated cells was accompanied by inducible NO synthase mRNA and protein accumulation. In the presence of N6, 2'-O-dibutyryladenosine 3',5'-cyclic monophosphate (cAMP) (10(-3) M) or isoproterenol (10(-5) M), interleukin-1 beta-induced nitrite accumulation was further increased, but the effect of 2-chloroadenosine was not additive or synergistic. The protein kinase C inhibitor calphostin C did not inhibit the effect of 2-chloroadenosine. These results indicate that adenosine acts on A2 receptors and augments NO synthesis in interleukin-1 beta-stimulated cardiac myocytes, at least partially through a cAMP-dependent pathway.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 2-Chloroadenosine / pharmacology
  • Adenosine / pharmacology*
  • Animals
  • Animals, Newborn
  • Bucladesine / pharmacology
  • Cells, Cultured
  • Dactinomycin / pharmacology
  • Enzyme Inhibitors / pharmacology
  • Heart / drug effects
  • Humans
  • Interleukin-1 / pharmacology
  • Isoproterenol / pharmacology
  • Myocardium / cytology
  • Myocardium / metabolism*
  • Naphthalenes / pharmacology
  • Nitric Oxide / biosynthesis*
  • Nitrites / analysis
  • Protein Kinase C / antagonists & inhibitors
  • Purinergic P1 Receptor Antagonists
  • Purinergic P2 Receptor Antagonists
  • Rats
  • Rats, Sprague-Dawley
  • Recombinant Proteins / pharmacology
  • Stereoisomerism
  • Theophylline / analogs & derivatives
  • Theophylline / pharmacology
  • Xanthines / pharmacology
  • omega-N-Methylarginine / pharmacology*

Substances

  • Enzyme Inhibitors
  • Interleukin-1
  • Naphthalenes
  • Nitrites
  • Purinergic P1 Receptor Antagonists
  • Purinergic P2 Receptor Antagonists
  • Recombinant Proteins
  • Xanthines
  • 2-Chloroadenosine
  • KF 17837
  • Dactinomycin
  • omega-N-Methylarginine
  • Nitric Oxide
  • 8-cyclopentyl-1,3-dimethylxanthine
  • Bucladesine
  • Theophylline
  • Protein Kinase C
  • calphostin C
  • Adenosine
  • Isoproterenol