Hemodynamic and Natriuretic Responses to Intravenous Infusion of Dopamine in Patients with Essential Hypertension (The 11th Conference on the Pathogenesis of Hypertension)

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Author(s)

Abstract

In order to clarify the role of dopamine on the pathophysiology of essential hypertension, mean arterial pressure (MAP), heart rate (HR), urine volume (UV), urinary sodium excretion (UNaV), endogenous creatinine clearance (Ccr), fractional excretions of sodium (FENa), inorganic phosphorus (FEP) and potassium (FEK), plasma renin activity (PRA), plasma aldosterone concentration (PAC) and plasma noradrenaline concentration (PNA) were measured before and after intravenous infusion of dopamine (3 μg/kg/min, 60 min) in normotensive (NT) and essential hypertensive subjects (EHT). Following dopamine infusion, a significant decrease of MAP and an increase of HR were observed in EHT but not in NT. UV, UNaV, Ccr, FENa, FEP and FEK increased significantly in both NT and EHT, and changes in these except for Ccr were significantly greater in EHT than in NT. In EHT, following dopamine infusion, PNA was clearly elevated, but no remarkable change was found in PRA and PAC. A significantly positive correlation was found between UNaV and FENa or FEP, and between FENa and FEP, while no significant relation was observed between UNaV and Ccr, MAP or MAP before dopamine infusion. A significant inverse correlation between supine PRA before dopamine infusion and FENa or FEP and a positive correlation between age and FENa or FEP were also observed in these patients. The changes in UNaV positively correlated with FENa and FEP in both low renin (group L) and normal renin EHT (group N) and with Ccr in group N but not in group L. The mean values of FENa, FEP and FEK were significantly higher in group L as compared with those in age-matched group N. These results suggest that, since the enhanced response to infused dopamine may reflect reduced dopaminergic activity, attenuation of renal dopaminergic activity might exist and be involved through a disturbance of water-sodium metabolism, at least in part, in the pathophysiological mechanism in EHT, particularly in group L.

Journal

  • Japanese Circulation Journal

    Japanese Circulation Journal 46(5), p486-493, 1982-05

    Japanese Circulation Society

Codes

  • NII Article ID (NAID)
    110002565561
  • NII NACSIS-CAT ID (NCID)
    AA00690731
  • Text Lang
    ENG
  • ISSN
    00471828
  • NDL Article ID
    2489771
  • NDL Source Classification
    ZS21(科学技術--医学--内科学)
  • NDL Call No.
    Z54-B860
  • Data Source
    NDL  NII-ELS 
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