Regulation of Vasopressin Receptors in Deoxycorticosterone Acetate–Salt Hypertension

Since arginine vasopressin may play a role in mlneralocorticoid hypertension, we examined the effects of deoxycorticosterone acetate (DOCA)-salt on vasopressin V1 and V2 receptor binding and their second messengers, inositol phosphate and adenylate cyclase, respectively, in liver and kidney to deter...

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Veröffentlicht in:Hypertension (Dallas, Tex. 1979) Tex. 1979), 1992-10, Vol.20 (4), p.569-574
Hauptverfasser: Trinder, Deborah, Phillips, Paddy A, Risvanis, John, Stephenson, Jayne M, Johnston, Colin I
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Sprache:eng
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Zusammenfassung:Since arginine vasopressin may play a role in mlneralocorticoid hypertension, we examined the effects of deoxycorticosterone acetate (DOCA)-salt on vasopressin V1 and V2 receptor binding and their second messengers, inositol phosphate and adenylate cyclase, respectively, in liver and kidney to determine whether altered vasopressin receptor binding is pathogenetic in mineralocorticoid hypertension. The mean arterial blood pressure of mineralocorticoid (DOCA-salt)-treated rats (163±1 mm Hg) was increased compared with control salt-treated rats (salt) (122±1 mm Hg) and water-treated rats (120±1 mm Hg;p
ISSN:0194-911X
1524-4563
DOI:10.1161/01.HYP.20.4.569