
Achieving the goal of optimised renin system suppression: preclinical experience with a direct renin inhibitor.
Author(s) -
Friedrich C. Luft
Publication year - 2006
Publication title -
jraas. journal of the renin-angiotensin-aldosterone system/journal of the renin-angiotensin-aldosterone system
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.457
H-Index - 46
eISSN - 1752-8976
pISSN - 1470-3203
DOI - 10.3317/jraas.2006.032
Subject(s) - renin–angiotensin system , renin inhibitor , pharmacology , computer science , medicine , blood pressure
Aliskiren is the first orally available direct renin inhibitor and is a highly potent and specific inhibitor of human renin.The high specificity for human renin has resulted in considerable challenges in utilising animal models in preclinical studies. Both marmoset and spontaneously hypertensive rat models demonstrate the safety and efficacy of aliskiren in reducing blood pressure, although both models have drawbacks.The former are difficult to study, while the latter feature a renin that is less amenable to inhibition by a human-renin-specific drug. However, a double transgenic rat (dTGR) model has been shown to be extremely valuable in preclinical studies of aliskiren.These rats are designed to express genes for human renin and angiotensinogen. Preclinical studies in dTGR demonstrate the efficacy and safety of aliskiren, both as monotherapy and in combination with ACE inhibitors and ARBs in the treatment of hypertension. Direct renin inhibition with aliskiren improves kidney function and reduces left ventricular hypertrophy, and may have the potential to provide end-organ protection