Functional role of the soluble guanylyl cyclase alpha(1) subunit in vascular smooth muscle relaxation

Cardiovasc Res. 2007 Oct 1;76(1):149-59. doi: 10.1016/j.cardiores.2007.06.002. Epub 2007 Jun 12.

Abstract

Objective: Soluble guanylyl cyclase (sGC), the predominant receptor for nitric oxide (NO), exists in 2 active isoforms (alpha(2)beta(1) and alpha(1)beta(1)). In vascular tissue sGCalpha(1)beta(1) is believed to be the most important. The aim of our study was to investigate the functional importance of the sGCalpha(1)-subunit in vasorelaxation.

Methods: Aortic and femoral artery segments from male and/or female sGCalpha(1)(-/-) mice and wild-type littermates were mounted in a small-vessel myograph for isometric tension recording. This was supplemented with biochemical measurements of the cGMP concentration and sGC enzyme activity.

Results: The functional importance of sGCalpha(1)beta(1) was demonstrated by the significantly decreased relaxing effects of acetylcholine (ACh), sodium nitroprusside (SNP), S-nitroso-N-acetylpenicillamine (SNAP), NO gas, YC-1, BAY 41-2272 and T-1032 in the sGCalpha(1)(-/-) mice of both genders. Moreover, the basal and SNP-stimulated cGMP levels and basal sGC activity were significantly lower in the sGCalpha(1)(-/-) mice. However, the relaxing effects of NO, BAY 41-2272 and YC-1 seen in blood vessels from sGCalpha(1)(-/-) mice indicate a role for an sGCalpha(1)beta(1)-independent mechanism. The increase in sGC activity after addition of BAY 41-2272 and the inhibition of the ACh-, SNP-, SNAP- and NO gas-induced response by the sGC inhibitor 1H-[1,2,4]oxadiazolo[4,3-a]quinoxalin-1-one (ODQ) in the sGCalpha(1)(-/-) mice are observations suggesting that the sGCalpha(2)beta(1) isoform is also functionally active. However, the insignificant increase in cGMP in response to SNP and the non-upregulated sGCalpha(2) expression level in the sGCalpha(1)(-/-) mice suggest rather the involvement of (an) sGC-independent mechanism(s).

Conclusions: We conclude that sGCalpha(1)beta(1) is involved in the vasorelaxation induced by NO-dependent and NO-independent sGC activators in both genders. However, the remaining relaxation seen in the sGCalpha(1)(-/-) mice suggests that besides sGCalpha(1)beta(1) also the minor isoform sGCalpha(2)beta(1) and/or (an) sGC-independent mechanism(s) play(s) a substantial role.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acetylcholine / pharmacology
  • Animals
  • Aorta
  • Cyclic GMP / analysis
  • Cyclic GMP / metabolism
  • Female
  • Guanylate Cyclase / analysis
  • Guanylate Cyclase / antagonists & inhibitors
  • Guanylate Cyclase / physiology*
  • In Vitro Techniques
  • Indazoles / pharmacology
  • Isoenzymes / physiology*
  • Male
  • Mice
  • Mice, Knockout
  • Muscle, Smooth, Vascular / drug effects
  • Muscle, Smooth, Vascular / enzymology
  • Muscle, Smooth, Vascular / physiology*
  • NG-Nitroarginine Methyl Ester / pharmacology
  • Nitric Oxide / pharmacology
  • Nitric Oxide Donors / pharmacology
  • Nitroprusside / pharmacology
  • Oxadiazoles / pharmacology
  • Pyrazoles / pharmacology
  • Pyridines / pharmacology
  • Quinoxalines / pharmacology
  • Receptors, Cytoplasmic and Nuclear / analysis
  • Receptors, Cytoplasmic and Nuclear / antagonists & inhibitors
  • Receptors, Cytoplasmic and Nuclear / physiology*
  • S-Nitroso-N-Acetylpenicillamine / pharmacology
  • Soluble Guanylyl Cyclase
  • Vasodilator Agents / pharmacology

Substances

  • 1H-(1,2,4)oxadiazolo(4,3-a)quinoxalin-1-one
  • 3-(4-Amino-5-cyclopropylpyrimidine-2-yl)-1-(2-fluorobenzyl)-1H-pyrazolo(3,4-b)pyridine
  • Gucy1a2 protein, mouse
  • Indazoles
  • Isoenzymes
  • Nitric Oxide Donors
  • Oxadiazoles
  • Pyrazoles
  • Pyridines
  • Quinoxalines
  • Receptors, Cytoplasmic and Nuclear
  • Vasodilator Agents
  • 3-(5'-hydroxymethyl-2'-furyl)-1-benzylindazole
  • Nitroprusside
  • Nitric Oxide
  • S-Nitroso-N-Acetylpenicillamine
  • Guanylate Cyclase
  • Soluble Guanylyl Cyclase
  • Cyclic GMP
  • Acetylcholine
  • NG-Nitroarginine Methyl Ester