(Hypertension. 1996;27:360-363.)
© 1996 American Heart Association, Inc.
Articles |
From the Department of Geriatric Medicine, Osaka (Japan) University Medical School.
Abstract The effect of human parathyroid hormonerelated protein, a powerful vasodilator, on endothelin-1 production in cultured bovine pulmonary arterial endothelial cells was studied. Treatment with parathyroid hormonerelated protein(1-34) at concentrations of 10-9 to 10-6 mol/L for 24 hours caused dose-dependent suppression of the secretion of endothelin-1, with maximal suppression at 10-7 mol/L to 74% of the control value. This inhibitory effect was completely abolished by coincubation with 100 ng/mL pertussis toxin, an inhibitor of GTP binding protein. Furthermore, addition of NG-monomethyl-L-arginine, an inhibitor of nitric oxide synthase, at 10-3 mol/L significantly blocked the suppressive effect of parathyroid hormonerelated protein(1-34) on endothelin-1 secretion, and further addition of 5x10-3 mol/L L-arginine significantly attenuated the blocking effect of NG-monomethyl-L-arginine. Parathyroid hormonerelated protein(1-34) at 10-7 mol/L resulted in an approximately fivefold increase in intracellular cGMP level. Northern blot analysis revealed that parathyroid hormonerelated protein(1-34) inhibited both basal and thrombin-induced endothelin-1 gene expression. These findings suggest that the vasodilating property of parathyroid hormonerelated protein may be mediated in part through its inhibitory effect on endothelin-1 production, which is probably mediated through nitric oxide and cGMP in endothelial cells. Thus, a feedback regulatory mechanism may exist between parathyroid hormonerelated protein and endothelin-1 in the vascular wall.
Key Words: parathyroid hormone endothelins nitric oxide pertussis toxins
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