This Article Figures Only Full Text Full Text (PDF) Alert me when this article is cited Alert me if a correction is posted Services Email this article to a friend Similar articles in this journal Similar articles in Web of Science Similar articles in PubMed Alert me to new issues of the journal Download to citation manager Citing Articles Citing Articles via HighWire Citing Articles via Web of Science (24) Citing Articles via Google Scholar Google Scholar Articles by Gradman, A. H. Articles by Kad, R. Search for Related Content PubMed PubMed Citation Articles by Gradman, A. H. Articles by Kad, R.

STATE-OF-THE-ART PAPER

Renin Inhibition in Hypertension

Division of Cardiovascular Diseases, The Western Pennsylvania Hospital, Pittsburgh, Pennsylvania.

Manuscript received October 18, 2007; accepted October 24, 2007.

^_* Reprint requests and correspondence: Dr. Alan H. Gradman, The Western Pennsylvania Hospital, 4800 Friendship Avenue, North Tower, Suite 3411, Pittsburgh, Pennsylvania 15224. (Email: gradmanmd{at}aol.com).

Fifty years ago, investigators identified renin inhibition as the preferred pharmacologic approach to blockade of the renin–angiotensin system. Renin is a monospecific enzyme that catalyzes the rate-limiting step in the synthesis of angiotensin II. Amplified enzymatic activity and additional physiological effects occur when renin and pro-renin bind to the (pro)renin receptor. Until very recently, development of clinically effective renin inhibitors remained elusive. Molecular modeling was used to develop aliskiren, a potent, low-molecular-weight, nonpeptide, direct renin inhibitor with sufficient bioavailability to produce sustained suppression of plasma renin activity after oral administration. In patients with hypertension, aliskiren produces dose-dependent blood pressure (BP) reduction and 24-h BP control up to a dose of approximately 300 mg once daily; at these doses, aliskiren shows placebo-like tolerability. Its antihypertensive potency is approximately equivalent to that of angiotensin receptor blockers, angiotensin-converting enzyme inhibitors, and diuretics. After abrupt withdrawal, persistent BP reduction and prolonged suppression of plasma renin activity is observed. When combined with diuretics, fully additive BP reduction is seen. When given with an angiotensin receptor blocker, aliskiren produces significant additional BP reduction indicative of complimentary pharmacology and more complete renin–angiotensin system blockade. Clinical trials are currently underway assessing the effects of aliskiren combined with an angiotensin receptor blocker on intermediate markers of end organ damage, and long-term end point trials are planned. The results of these studies will ultimately determine the place of renin inhibition and aliskiren in the treatment of hypertension and related cardiovascular disorders. The effect of aliskiren on receptor-bound renin and pro-renin is the subject of active investigation.

Abbreviations and Acronyms   A I/II = angiotensin I/II   ACE = angiotensin-converting enzyme   BP = blood pressure   Cmax = maximum serum concentration   dTGR = double transgenic rats   HCTZ = hydrochlorothiazide   LVH = left ventricular hypertrophy   PAI = plasminogen activator inhibitor   PRA = plasma renin activity   PRC = plasma renin concentration   RAS = renin–angiotensin system   TGF = transforming growth factor

This article has been cited by other articles:

				N. Ferri, C. M. Greco, G. Maiocchi, and A. Corsini Aliskiren reduces prorenin receptor expression and activity in cultured human aortic smooth muscle cells Journal of Renin-Angiotensin-Aldosterone System, December 1, 2011; 12(4): 469 - 474. [Abstract] [PDF]

				M. Auron, B. Harte, A. Kumar, and F. Michota Renin-angiotensin system antagonists in the perioperative setting: clinical consequences and recommendations for practice Postgrad. Med. J., July 1, 2011; 87(1029): 472 - 481. [Abstract] [Full Text] [PDF]

				K. C. Wu and G. Gerstenblith Review: Update on Newer Antihypertensive Medicines and Interventions Journal of Cardiovascular Pharmacology and Therapeutics, September 1, 2010; 15(3): 257 - 267. [Abstract] [PDF]