Several imidazole derivatives that bind specifically to the angiotensin II
type 1 receptor (the angiotensin receptor blockers, or ARE), have been deve
loped in recent years and made available to clinicians. Preclinical studies
revealed some differences in pharmacokinetic parameters and in vitro effec
ts, However, most of the reported physiologic effects associated with ARE a
dministration are similar to those of angiotensin-converting enzyme inhibit
ors (ACEI). In short-term clinical studies, the efficacy of ARE in reducing
BP (BP) was similar to that of the ACEI, whereas (with a few exceptions) t
he side-effect profile was comparable to that of placebo. Whether targeting
antihypertensive treatment with such a high specificity within the renin c
ascade carries major clinical advantages over inhibiting angiotensin-conver
ting enzyme remains to be demonstrated.