S. Gupta et al., ROLE OF ENDOTHELIUM-DERIVED NITRIC-OXIDE IN STIMULATION OF NA-K+-ATPASE ACTIVITY BY ENDOTHELIN IN RABBIT AORTA(), The American journal of physiology, 266(2), 1994, pp. 80000577-80000582
An endothelium-derived factor with the properties of nitric oxide (NO)
has recently been implicated in the regulation of basal Na+-K+-adenos
inetriphosphatase (ATPase) activity in vascular smooth muscle. To dete
rmine whether this factor also plays a role in the stimulation of ouab
ain-sensitive (OS) Rb-86 uptake by specific agonists, studies were car
ried out using rabbit aortic rings. In endothelium-intact rings incuba
ted for 3 h with Krebs-Henseleit solution containing 5.5 mM glucose, e
ndothelin (ET) caused a concentration-dependent increase in OS Rb-86 u
ptake (maximal increase = 205%, with 100 nM ET). Incubation with pheny
lephrine (Phe; 0.1 and 1 mu M) or phorbol 12,13-dibutyrate (PDBu; 0.1
CLM), under the same conditions, increased OS Rb-86 uptake by 128, 144
, and 140%, respectively. Removal of endothelium before incubation dec
reased the ability of ET to stimulate OS Rb-86 uptake by 38-45%, but i
t did not diminish the stimulation of OS Rb-86 uptake by Phe or PDBu.
An increase in the concentration of glucose from 5.5 to 44 mM diminish
ed ET-stimulated OS Rb-86 uptake by 50% in endothelium-intact rings bu
t had no effect on Phe- or PDBu-induced increases in OS Rb-86 uptake.
Addition of the NO synthase inhibitor NG-monomethyl-L-arginine (L-NMMA
; 0.3 mM) to the medium decreased ET-stimulated OS Rb-86 uptake by 40%
. Guanosine 3',5'-cyclic monophophate (cGMP) formation in endothelium-
intact rings was also increased (65%) by ET but not by Phe or PDBu. Th
e increase in cCMP by ET was totally inhibited by L-NMMA or endotheliu
m denudation. These results indicate that the stimulation of Na+-K+-AT
Pase activity in the rabbit aorta by ET is in part endothelium depende
nt. They suggest that ET acts by increasing the release of NO and that
this component of its effect on aortic Na+-K+-ATPase activity is inhi
bited by hyperglycemia.