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Hypertension. 2000;35:732-739

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(Hypertension. 2000;35:732.)
© 2000 American Heart Association, Inc.


Scientific Contributions

Mechanisms of Big Endothelin-1–Induced Diuresis and Natriuresis

Role of ETB Receptors

Aaron Hoffman; Zaid A. Abassi; Sergey Brodsky; Rawi Ramadan; Joseph Winaver

From the Department of Vascular Surgery (A.H., Z.A.A.), Rambam Medical Center, Haifa, Israel; Department of Physiology and Biophysics (Z.A.A., S.B., J.W.), The Bruce Rappaport Faculty of Medicine, Technion-Israel Institute of Technology, Haifa, Israel; and Department of Nephrology (R.R.), Poriah Government Hospital, Tiberias, Israel.

Correspondence to Aaron Hoffman, MD, Department of Vascular Surgery, Rambam Medical Center, POB 9602, 31096 Haifa, Israel. E-mail ahofman{at}rambam.health.gov.il

Abstract—Endothelin-1 (ET-1) at high concentrations has marked antidiuretic and antinatriuretic activities, whereas its precursor, big endothelin-1 (big ET-1), has surprisingly potent diuretic and natriuretic actions. The mechanisms underlying the excretory effects of big ET-1 have not been fully elucidated. To explore these mechanisms, we examined the effects of a highly selective ETB antagonist (A-192621.1), a calcium channel blocker (verapamil), a nitric oxide synthase inhibitor (N-nitro-L-arginine methyl ester [L-NAME]), and a cyclooxygenase inhibitor (indomethacin) on the systemic and renal actions of big ET-1 in anesthetized rats. An intravenous bolus injection of incremental doses of big ET-1 (0.3, 1.0, and 3.0 nmol/kg) produced a significant hypertensive effect that was dose dependent and prolonged (from 113±7 mm Hg to a maximum of 148±6 mm Hg). The administration of big ET-1 induced marked diuretic and natriuretic responses (urinary flow rate increased from 8.5±1 to 110±14 µL/min, and fractional excretion of sodium increased from 0.38±0.13% to 7.51±1.24%). Glomerular filtration rate and renal plasma flow significantly decreased only at the highest dose of big ET-1. Pretreatment with A-192621.1 (3 mg/kg plus 3 mg · kg-1 · h-1) significantly abolished the diuretic (17±5 µL/min to a maximum of 19±3 µL/min) and natriuretic (0.29±0.1% to a maximum of 1.93±0.37%) responses induced by big ET-1. Moreover, A-192621.1 potentiated the decline in glomerular filtration rate and renal plasma flow and the increase in mean arterial blood pressure produced by the low doses of big ET-1. Similar to A-192621.1, pretreatment with a nitric oxide synthase inhibitor (L-NAME, 10 mg/kg plus 5 mg · kg-1 · h-1) significantly and comparably reduced the diuretic and natriuretic actions of big ET-1 and augmented the hypoperfusion/hypofiltration and systemic vasoconstriction induced by high doses of the peptide. Pretreatment with verapamil (2 mg · kg-1 · h-1) slightly inhibited the diuretic/natriuretic effects of the high-dose big ET-1 and completely prevented the increase in mean arterial blood pressure provoked by the peptide. Unlike verapamil and L-NAME, only indomethacin administration was associated with significant natriuretic/diuretic responses and did not influence the pressor effect and renal actions of big ET-1. Taken together, these results suggest that big ET-1–induced diuretic and natriuretic responses are mediated mainly by stimulation of nitric oxide production coupled to ETB receptor subtype activation.


Key Words: endothelin • receptors, endothelin • nitric oxide • verapamil • prostaglandins • diuretics




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