Different activation of L-arginine pathway by bradykinin, serotonin, and clonidine in coronary arteries

Am J Physiol. 1990 Nov;259(5 Pt 2):H1433-9. doi: 10.1152/ajpheart.1990.259.5.H1433.

Abstract

Endothelial cells release nitric oxide from L-arginine, and this pathway can be inhibited by the analogue of L-arginine, NG-monomethyl-L-arginine (L-NMMA). The effect of L-NMMA on endothelium-dependent relaxation of epicardial porcine coronary arteries was studied in isolated blood vessels suspended in organ chambers for isometric tension recording. Endothelium-dependent relaxations to bradykinin, serotonin, and the alpha 2-adrenergic agonist clonidine were evaluated in the presence and absence of L-NMMA (10(-5)-10(-3) M). L-NMMA, as well as the inhibitor of guanylate cyclase methylene blue (10(-5) M) and hemoglobin (10(-5) M), inhibited endothelium-dependent relaxation to serotonin and clonidine. The effect of L-NMMA could be reversed by L-arginine but not by D-arginine. In contrast, L-NMMA, methylene blue, and hemoglobin caused a weak inhibition of the endothelium-dependent relaxation evoked by bradykinin; indomethacin and tranylcypromine had no effect. The inhibitor of Gi proteins pertussis toxin (100 ng/ml) abolished the relaxations evoked by clonidine and markedly reduced those evoked by serotonin but did not affect those caused by bradykinin. In the presence of pertussis toxin, L-NMMA induced a further reduction of the relaxations to serotonin, suggesting that inhibition of Gi proteins does not completely prevent the activation of the L-arginine pathway. Thus endothelium-dependent relaxations to serotonin and to the alpha 2-adrenergic agonist clonidine are mediated through the release of nitric oxide formed from L-arginine in endothelial cells, whereas bradykinin evokes endothelium-dependent relaxations via a different pathway.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenosine Triphosphate / pharmacology
  • Animals
  • Arginine / metabolism*
  • Bradykinin / pharmacology*
  • Clonidine / pharmacology*
  • Coronary Vessels / metabolism*
  • GTP-Binding Proteins / physiology
  • Potassium Channels / physiology
  • Prostaglandin-Endoperoxide Synthases / metabolism
  • Serotonin / pharmacology*
  • Swine

Substances

  • Potassium Channels
  • Serotonin
  • Adenosine Triphosphate
  • Arginine
  • Prostaglandin-Endoperoxide Synthases
  • GTP-Binding Proteins
  • Clonidine
  • Bradykinin