Both candoxatrilat and SC 46542 markedly potentiated the natriuretic response to brain natriuretic peptide in conscious rats, though SC 46542 had a shorter duration of effect.
Does candoxatrilat or SC 46542 potentiate the renal and blood pressure response to BNP in conscious rats?
Inhibition of endopeptidase-24.11 or the ANP clearance receptor potentiates the natriuretic activity of BNP, suggesting BNP may mediate some effects of E-24.11 inhibitors in heart failure.
The present studies examined the effect of (a) a specific endopeptidase-24.11 (E-24.11) inhibitor (candoxatrilat) and (b) a ligand for the atrial natriuretic peptide (ANP) clearance receptor (SC 46542) on the renal and blood pressure response to brain natriuretic peptide (BNP) in conscious rats. 2. Infusion of BNP 200 ng kg-1 min-1 for 60 min produced a small rise in urinary sodium and guanosine 3':5'-cyclic monophosphate (cyclic GMP) excretion with a non-significant fall in mean arterial blood pressure. 3. Candoxatrilat (3 mg kg-1) alone had no significant effect on sodium excretion or blood pressure but markedly potentiated the natriuretic response to BNP. 4. Similarly SC 46542 (68 micrograms kg-1; 6.8 micrograms kg-1 min-1) which produced no significant effect on its own, potentiated the natriuresis-induced by BNP, although the effect was of shorter duration compared to that of candoxatrilat. 5. The data indicate two approaches to the potentiation of the renal activity of BNP and suggest that BNP may mediate some of the activity of E-24.11 inhibitors reported in cardiac failure.
Kirk et al. (Wed,) reported a other. Candoxatrilat or SC 46542 with brain natriuretic peptide (BNP) vs. BNP alone was evaluated on Renal and blood pressure response (urinary sodium, cyclic GMP excretion, mean arterial blood pressure). Both candoxatrilat and SC 46542 markedly potentiated the natriuretic response to brain natriuretic peptide in conscious rats, though SC 46542 had a shorter duration of effect.
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