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Ciprokiren (Ro 44-9375). A renin inhibitor with increasing effects on chronic treatment.
Author(s) -
Walter Fischli,
JeanPaul Clozel,
Volker Breu,
Stefan Buchmann,
Sarah Mathews,
Heinz Stadler,
E. VIEIRA,
Wolfgang Wostl
Publication year - 1994
Publication title -
hypertension
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.986
H-Index - 265
eISSN - 1524-4563
pISSN - 0194-911X
DOI - 10.1161/01.hyp.24.2.163
Subject(s) - plasma renin activity , renin inhibitor , renin–angiotensin system , blood pressure , pharmacology , in vivo , endocrinology , ic50 , potency , chemistry , medicine , oral administration , hemodynamics , in vitro , biology , biochemistry , microbiology and biotechnology
The present study characterizes the new transition-state renin inhibitor ciprokiren (Ro 44-9375) in squirrel monkeys. Arterial blood pressure was monitored by telemetry in freely moving, chronically instrumented conscious animals. In vitro at pH 7.4, ciprokiren inhibited human renin in buffer and human plasma with an IC50 of 0.07 and 0.65 nmol/L, respectively. It was equipotent against primate plasma renin and also inhibited plasma renin from dog and guinea pig in the nanomolar range (IC50, 29 and 65 nmol/L, respectively). After acute oral administration it reduced arterial blood pressure dose dependently in normotensive sodium-depleted and cyclosporin-induced hypertensive squirrel monkeys, starting with the minimal oral dose of 3 micrograms/kg. Daily oral doses of 1 microgram/kg showed a progressive blood pressure decrease, with a maximal response reached after 1 week. The drug could also be applied transdermally with similar hemodynamic effects without any decrease of plasma renin activity or plasma immunoreactive angiotensin II. Thus, ciprokiren is characterized in squirrel monkeys as a renin inhibitor with high in vivo potency that might act mainly in the tissular compartment.

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