Clinical pharmacology of atrial natriuretic (3-28) eicosahexapeptide.

J Biollaz, J Nussberger, B Waeber… - Journal of hypertension …, 1986 - europepmc.org
J Biollaz, J Nussberger, B Waeber, HR Brunner
Journal of hypertension. Supplement: Official Journal of the …, 1986europepmc.org
The clinical pharmacology of a synthetic rat atrial natriuretic peptide (rANP) was evaluated in
normal volunteers. During a dose-ranging study at 1-40 micrograms/min we observed a
dose-dependent decrease in mean intra-arterial blood pressure, an acceleration of the heart
rate and a transient increase in blood flow to the skin. During a 4-h constant-dose infusion at
0.5 and 5.0 micrograms/min, inulin clearance remained unchanged but there was a dose-
related fall in paraaminohippurate (PAH) clearance and an increase in the filtration fraction …
The clinical pharmacology of a synthetic rat atrial natriuretic peptide (rANP) was evaluated in normal volunteers. During a dose-ranging study at 1-40 micrograms/min we observed a dose-dependent decrease in mean intra-arterial blood pressure, an acceleration of the heart rate and a transient increase in blood flow to the skin. During a 4-h constant-dose infusion at 0.5 and 5.0 micrograms/min, inulin clearance remained unchanged but there was a dose-related fall in paraaminohippurate (PAH) clearance and an increase in the filtration fraction. Urinary excretion of sodium, chloride and calcium increased in a dose-related fashion, but with the high dose the excretion curve had a bell-shape. No change in plasma renin activity, angiotensin II and aldosterone was observed during the rANP infusion despite the excretion of large amounts of sodium and a blood pressure reduction with the high dose. Indocyanine green clearance, a measure of hepatic blood flow, was significantly decreased by a 2-h rANP infusion at 1.0 microgram/min. In normal volunteers, therefore, rANP induced vasodilation and blood pressure reduction, a decrease in renal and hepatic blood flow and a natriuretic and transient diuretic effect without activation of the renin-angiotensin-aldosterone system.
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