Hypertension, Vol 22, 119-126, Copyright © 1993 by American Heart Association
AM Richards, IG Crozier, T Kosoglou, M Rallings, EA Espiner, MG Nicholls, TG Yandle, H Ikram and C Frampton
The detailed integrated renal, hormonal, and hemodynamic effects of acute
(first dose) and established (4 days) inhibition of endopeptidase 24.11 by
SCH 42495 (200 mg, every 12 hours) were documented in eight patients with
essential hypertension in a double-blind, balanced random- order, crossover
study. SCH 42495 suppressed plasma endopeptidase activity (> 90%, P <
.001) for the duration of the dosing period. Initially, plasma atrial
natriuretic factor levels increased markedly (+123%, P < .01) and
remained elevated, although to a lesser extent (+34%, P < .01), with
established enzyme inhibition. Cyclic guanosine monophosphate in both
plasma and urine remained elevated throughout the treatment period.
Significant augmentation of sodium excretion in excess of placebo values
(96 +/- 27 mmol sodium, P < .001) was established in the initial 24
hours of dosing but later became attenuated, with a mild antinatriuresis (P
< .01) in the latter 3 days of treatment. Blood pressure, heart rate,
the renin-angiotensin- aldosterone system, and plasma norepinephrine levels
were all initially (first dose) unchanged. With established enzyme
inhibition (day 4), however, blood pressure was significantly lower (mean
24-hour values, 9.3 +/- 3/-3.8 +/- 1 mm Hg, P < .05 for both systolic
and diastolic pressures) than matched placebo values, whereas heart rate
was higher (2.7 +/- 1 beats per minute, P < .01). Mean 24-hour values of
plasma renin activity (+33%, P < .05), aldosterone (+36%, P < .05),
and norepinephrine (+40%, P < .001) were all clearly increased above
placebo values with established enzyme inhibition.(ABSTRACT TRUNCATED AT
250 WORDS)
ARTICLES
Endopeptidase 24.11 inhibition by SCH 42495 in essential hypertension
Department of Cardiology, Princess Margaret Hospital, Christchurch, New Zealand.
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