Vasoconstrictors and nitrovasodilators reciprocally regulate the Na+-K+-2Cl(-) cotransporter in rat aorta

Akar F., Skinner E., Klein J., Jena M., Paul R., O'Neill W.

AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, vol.276, no.6, 1999 (SCI-Expanded) identifier identifier identifier

  • Publication Type: Article / Article
  • Volume: 276 Issue: 6
  • Publication Date: 1999
  • Doi Number: 10.1152/ajpcell.1999.276.6.c1383
  • Journal Indexes: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Keywords: sodium-potassium-chloride cotransport, vascular smooth muscle, contraction, cell chloride, phenylephrine, angiotensin II, endothelin, nitric oxide, SMOOTH-MUSCLE CELLS, K-CL COTRANSPORT, VASCULAR ENDOTHELIAL-CELLS, ATRIAL NATRIURETIC FACTOR, ANGIOTENSIN-II, INTRACELLULAR CHLORIDE, NA+/K+/CL COTRANSPORT, PRIMARY HYPERTENSION, SALT HYPERTENSION, FUROSEMIDE
  • Gazi University Affiliated: Yes


Little is known about the function and regulation of the Na+-K+-2Cl(-) cotransporter NKCC1 in vascular smooth muscle. The activity of NKCC1 was measured as the bumetanide-sensitive efflux of Rb-86(+) from intact smooth muscle of the rat aorta. Hypertonic shrinkage (440 mosmol/kgH(2)O) rapidly doubled cotransporter activity, consistent with its volume-regulatory function. NKCC1 was also acutely activated by the vasoconstrictors ANG II (52%), phenylephrine (50%), endothelin (53%), and 30 mM KCl (54%). Both nitric oxide and nitroprusside inhibited basal NKCC1 activity (39 and 34%, respectively), and nitroprusside completely reversed the stimulation by phenylephrine. The phosphorylation of NKCC1 was increased by hypertonic shrinkage, phenylephrine, and KCl and was reduced by nitroprusside. The inhibition of NKCC1 significantly reduced the contraction of rat aorta induced by phenylephrine (63% at 10 nM, 26% at 30 nM) but not by KCl. We conclude that the Na+-K+-2Cl(-) cotransporter in vascular smooth muscle is reciprocally regulated by vasoconstrictors and nitrovasodilators and contributes to smooth muscle contraction, indicating that alterations in NKCC1 could influence vascular smooth muscle tone in vivo.