Literature DB >> 27126389

Drug discovery in renin-angiotensin system intervention: past and future.

Bryan Williams1.   

Abstract

The renin-angiotensin system (RAS) plays a central role in the control of blood pressure in the body and the way this interacts with other systems is widely recognized. This has not always been the case and this review summarizes how our knowledge has evolved from the initial discovery of renin by Tigerstedt and Berman in 1898. This includes the identification of angiotensin in the 1950s to the proposed relationship between this system, hypertension and ultimately cardiovascular disease. While the RAS is far more complex than originally thought, much is now known about this system and the wide ranging effects of angiotensin in the body. This has enabled the development of therapies that target the various proteins in this pathway and hence are implicated in disease. The first of these treatments was the angiotensin converting enzyme inhibitors (ACE-Is), followed by the angiotensin receptor blockers (ARBs), and more recently the direct renin inhibitors (DRIs). Clinical outcome trials have shown these drugs to be effective, but as they act at contrasting points in the RAS, there are differences in their efficacy and safety profiles. RAS blockade is the foundation of modern combination therapy with a calcium channel blocker and/or a diuretic given to reduce blood pressure and limit the impact of RAS activation. Other options that complement these treatments may be available in the future and will offer more choice to clinicians.
© The Author(s), 2016.

Entities:  

Keywords:  angiotensin II; cardiovascular remodelling; renin–angiotensin system (RAS)

Mesh:

Substances:

Year:  2016        PMID: 27126389      PMCID: PMC5933671          DOI: 10.1177/1753944716642680

Source DB:  PubMed          Journal:  Ther Adv Cardiovasc Dis        ISSN: 1753-9447


  40 in total

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Journal:  Blood Press       Date:  2013-12-20       Impact factor: 2.835

3.  Activity of various fractions of bradykinin potentiating factor against angiotensin I converting enzyme.

Authors:  S H Ferreira; L H Greene; V A Alabaster; Y S Bakhle; J R Vane
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4.  Stimulation of angiotensin AT2 receptors by the non-peptide agonist, Compound 21, evokes vasodepressor effects in conscious spontaneously hypertensive rats.

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8.  Effects of valsartan on morbidity and mortality in patients with heart failure not receiving angiotensin-converting enzyme inhibitors.

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Journal:  J Am Coll Cardiol       Date:  2002-10-16       Impact factor: 24.094

9.  Valsartan, captopril, or both in myocardial infarction complicated by heart failure, left ventricular dysfunction, or both.

Authors:  Marc A Pfeffer; John J V McMurray; Eric J Velazquez; Jean-Lucien Rouleau; Lars Køber; Aldo P Maggioni; Scott D Solomon; Karl Swedberg; Frans Van de Werf; Harvey White; Jeffrey D Leimberger; Marc Henis; Susan Edwards; Steven Zelenkofske; Mary Ann Sellers; Robert M Califf
Journal:  N Engl J Med       Date:  2003-11-10       Impact factor: 91.245

Review 10.  Emergence and evolution of the renin-angiotensin-aldosterone system.

Authors:  David Fournier; Friedrich C Luft; Michael Bader; Detlev Ganten; Miguel A Andrade-Navarro
Journal:  J Mol Med (Berl)       Date:  2012-04-14       Impact factor: 4.599

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Review 4.  Angiotensin-converting enzyme 2 (ACE2): SARS-CoV-2 receptor and RAS modulator.

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Review 6.  Effects of Olive Oil on Blood Pressure: Epidemiological, Clinical, and Mechanistic Evidence.

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