The adrenomedullary venous vasculature as a target for endothelins: comparison of the porcine and bovine central adrenomedullary veins

Comp Biochem Physiol A Mol Integr Physiol. 1998 Jul;120(3):439-46. doi: 10.1016/s1095-6433(98)10044-2.

Abstract

The functional properties of the isolated porcine and bovine central adrenomedullary veins were compared, with emphasis on the active tension responses to high K+, endothelin-1 (ET-1) and neuropeptide Y (NPY). In the porcine vein, the contraction evoked by ET-1 was 4--5-fold higher than with high K+, as in the bovine vein. The potencies for ET-1 were similar in ring and strip preparations of the porcine vein, with EC50 values 5--7-fold higher than in the bovine vein. In preparations previously exposed to ET-1 the contractions evoked by high K+ and NPY were potentiated and facilitated, respectively,. However, only in the porcine vein was the ET-1 contraction sustained. This contraction was effectively relaxed by milrinone, indicating a role for cGMP inhibited cyclic nucleotide phosphodiesterase in the sustained contraction. Caffeine and forskolin were also effective relaxants of contractions evoked by ET-1 in both veins, suggesting relaxation by elevated levels of cAMP. The K(+)-contracted porcine, but not bovine, vein was relaxed by acetylcholine (ACh) and vasointestinal polypeptide in a concentration-dependent manner, indicating species differences with respect to signal transduction leading to increases in cyclic nucleotides. In conclusion, these results demonstrate that ET-1 is the main constrictor of the porcine central adrenomedullary vein, with significant species differences in mode of contraction and relaxation. These findings suggest roles for the endogeneously released ET-1 and NPY in regulation of venous contractility within the adrenal gland of mammals.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acetylcholine / pharmacology
  • Adenylyl Cyclases / metabolism
  • Adrenal Medulla / blood supply*
  • Animals
  • Caffeine / pharmacology
  • Cattle / physiology*
  • Colforsin / pharmacology
  • Cyclic AMP / physiology
  • Endothelin-1 / pharmacology*
  • Milrinone / pharmacology
  • Muscle, Smooth, Vascular / drug effects
  • Neuropeptide Y / pharmacology
  • Potassium / pharmacology
  • Propranolol / pharmacology
  • Receptor, Endothelin A
  • Receptors, Endothelin / drug effects
  • Receptors, Endothelin / physiology
  • Second Messenger Systems / physiology
  • Species Specificity
  • Swine / physiology*
  • Vasoactive Intestinal Peptide / pharmacology
  • Vasoconstriction / drug effects*
  • Vasoconstrictor Agents / pharmacology
  • Vasodilation / drug effects
  • Vasodilator Agents / pharmacology
  • Veins / drug effects

Substances

  • Endothelin-1
  • Neuropeptide Y
  • Receptor, Endothelin A
  • Receptors, Endothelin
  • Vasoconstrictor Agents
  • Vasodilator Agents
  • Colforsin
  • Vasoactive Intestinal Peptide
  • Caffeine
  • Propranolol
  • Cyclic AMP
  • Adenylyl Cyclases
  • Milrinone
  • Acetylcholine
  • Potassium