Why the study?
Does human BNP infusion, NEP inhibition, or their combination alter hemodynamic, hormonal, and renal parameters in patients with left ventricular impairment?
Does human BNP infusion, NEP inhibition, or their combination alter hemodynamic, hormonal, and renal parameters in patients with left ventricular impairment?
BNP infusion and NEP inhibition induce significant hemodynamic and renal responses in left ventricular impairment, but their combination blunts the natriuretic response due to an augmented hypotensive effect.
Supports BNP-NEP combination for enhanced cGMP in LV impairment; extends mechanistic evidence for targeted heart failure therapies.
Brain natriuretic peptide (BNP) is increased in left ventricular impairment and neutral endopeptidase (NEP) is involved in its metabolism. In random order, eight patients with left ventricular impairment received placebo, a 4-h infusion of human BNP (3.0 pmol/kg min), a single oral dose of NEP inhibitor (SCH 42495, 300 mg), and combined BNP and SCH 42495. Plasma BNP, cGMP, and cortisol were significantly increased by all three treatments (P < 0.05-P < 0.001). Combined treatment had a synergistic effect on plasma cGMP. The metabolic clearance rate of exogenous BNP was reduced (25%) by NEP inhibition. Endogenous plasma ANP was augmented more than BNP by NEP inhibition. Plasma aldosterone, unchanged during infusions, rose markedly after BNP and after the combined treatment (P < 0.05 for both). Urine sodium excretion, increased by NEP inhibition (P < 0.05) and by BNP (P = 0.05), was unchanged during combined treatment. Urine cGMP excretion was increased, whereas blood pressure was reduced by all active treatments (P < 0.05-0.01 for all). Heart rate increased only with combined treatment (P = 0.007). Plasma renin activity, norepinephrine, and cardiac output were unaffected. BNP infusion and NEP inhibition both induced significant hemodynamic and renal responses. The augmented hypotensive effect of combined treatments, and consequent fall in renal perfusion pressure, may underly the observed blunting of the natriuretic response that occurred despite greater than additive increments in plasma BNP, ANP, and cGMP.
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Lainchbury et al. (1999) studied this question.
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