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Low-dose infusion of atrial natriuretic factor in mild essential hypertension

Tonolo, Giancarlo and Richards, A. M. and Manunta, Paolo and Troffa, Chiara and Pazzola, A. and Madeddu, Paolo Roberto and Towrie, A. and Fraser, Robert and Glorioso, Nicola (1989) Low-dose infusion of atrial natriuretic factor in mild essential hypertension. Circulation, Vol. 80 (4), p. 893-902. eISSN 1524-4539. Article.

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Intra-arterial blood pressure, cardiac output, heart rate, right heart indexes, urinary electrolytes, and urinary volume were monitored in eight patients with untreated (WHO Class I) essential hypertension. The patients were given synthetic atrial natriuretic factor (ANF) (99-126 [alpha] -hANP) at 1 and 2 pmol/kg/min in series (phases 1 and 2, 2 hours each dose) or vehicle (hemaccel) in random order on two separate occasions while on their usual diet. Arterial plasma ANF levels increased significantly from basal and time-matched placebo values from 25+/-2 and 28+/-3 pmol /l to 50+/-4 and 83+/-9 pmol/l at the end of phases 1 and 2,respectively (p < 0.001). After 30 minutes during phase 2, systolic blood pressure decreased significantly by 20+/-4 mm Hg (p < 0.001) from basal and time-matched placebo values and remained significantly reduced (-17+/-4 mm Hg, p < 0.001) by the end of the recovery period (2 hours after infusions were completed). Pulmonary systolic blood pressure decreased by 5+/-1 mm Hg (phase 2, p < 0.05). Cardiac output decreased by 0.5+/-0.1 l/min below baseline at the end of phase 2 ofANF infusion, whereas it increased significantly (p < 0.02) by 0.6+/-0.1 l/min during vehicle infusion. Systemic diastolic, pulmonary diastolic, right atrial, and wedge pressures were not significantly changed during ANF or vehicle infusions, nor were pulmonary vascular resistance or heart rate altered. Systemic vascular resistance did not change significantly during both infusions, whereas during recovery, systemic vascular resistance decreased significantly after ANF infusion was discontinued (p < 0.05). Microhematocrit levels increased dose dependently during ANF. The maximum increase was observed at the end of phase 2 (+4.7+/-1.7%), whereas the microhematocrit level decreased to -2.4+/-0.6% with vehicle (p+/-0.001) at the end of phase 2. Urinary sodium excretion increased significantly (p < 0.02) by the end of phase 2 under ANF infusion (+38+/-15%), whereas it decreased (-10+/-6%) under placebo infusion by the end of phase 2. Urinary magnesium excretion was significantly increased during ANF infusion from phase 1 (p < 0.02), whereas urinary potassium levels, calcium levels, creatinine levels, volume, and glomerular filtration rate did not difer significantly between the two infusions. Plasma renin, angiotensin H, aldosterone, and catecholamine concentrations did not change significantly during ANF or vehicle infusions. Our data suggest that increases in circulating arterial ANF levels to the upper limit of the ranges reported for humans with hypertension in absence of cardiac or renal failure reduce plasma volume and exert a selective lowering effect on systolic blood pressure without changing calculated peripheral vascular resistances.

Item Type:Article
ID Code:191
Uncontrolled Keywords:Atrial natriuretic factor, cardiac output, hypertension, blood pressure, pulmonary
Subjects:Area 06 - Scienze mediche > MED/11 Malattie dell'apparato cardiovascolare
Divisions:001 Università di Sassari > 03 Istituti > Clinica medica generale e terapia medica
Publisher:Lippincott Williams & Wilkins
Copyright Holders:© 1989 American Heart Association
Deposited On:18 Aug 2009 10:01

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