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Updated: Jul 20, 2026

Receptor Autoradiography Protocol for the Localized Visualization of Angiotensin II Receptors
Published on: June 7, 2016
Clinical evidence for the cardiovascular benefits of angiotensin receptor blockers
Georg Nickenig1, Jan Ostergren, Harry Struijker-Boudier
1University of Saarland, Homburg, Germany.
Insights
Angiotensin II receptor blockers (ARBs) offer a well-tolerated approach to managing cardiovascular disease (CVD). They effectively block harmful effects, potentially delaying diabetes and reducing CVD risks.
Area of Science:
- Cardiovascular Medicine
- Pharmacology
Background:
- The renin-angiotensin-aldosterone system (RAAS) and its effector peptide, angiotensin II (Ang II), are key targets for cardiovascular disease (CVD) management.
- Angiotensin II contributes to CVD progression, morbidity, and mortality.
- Current strategies include ACE inhibitors (ACE-Is) and Ang II receptor blockers (ARBs).
Purpose of the Study:
- To evaluate the role of targeting Ang II in slowing CVD progression.
- To compare the efficacy and tolerability of ACE inhibitors versus Ang II receptor blockers.
- To explore the potential of ARBs in preventing or delaying diabetes.
Main Methods:
- Review of numerous clinical studies and trials investigating ACE inhibitors and ARBs.
- Analysis of outcomes related to morbidity and mortality in cardiovascular disease patients.
- Assessment of tolerability profiles, including adverse effects like angioedema and cough.
Main Results:
- ACE inhibitors demonstrate benefits in reducing CVD morbidity and mortality but have tolerability concerns.
- ARBs provide a more specific and complete blockade of Ang II's detrimental effects with generally better tolerability.
- Clinical trials indicate ARBs are associated with positive outcomes across the CVD spectrum and may help prevent or delay diabetes.
Conclusions:
- Targeting Ang II via ARBs is a promising strategy for managing cardiovascular disease.
- ARBs offer a favorable tolerability profile compared to ACE inhibitors.
- Further trials are ongoing to define the definitive role of ARBs in reducing CVD morbidity and mortality.
Abstract:
Targeting the renin-angiotensin-aldosterone system (RAAS), specifically the effector peptide angiotensin II (Ang II), represents a major opportunity for slowing the progression of cardiovascular disease (CVD) and, in turn, reducing the risk of morbidity and mortality. Inhibition of angiotensin-converting enzyme (ACE) and selective blockade of Ang II AT1 receptors are two approaches through which the pathophysiological effects of Ang II can be targeted. Numerous clinical studies have established the benefits of ACE inhibitors (ACE-Is) in lessening the morbidity and mortality burden of CVD. There are, however, tolerability concerns associated with ACE-Is, such as angioedema and dry cough. By blocking Ang II at the AT1 receptor level, Ang II receptor blockers (ARBs) provide a more specific and complete blockade of the deleterious effects of Ang II and tend to have more favourable tolerability. A number of clinical trials have shown that ARBs are not only associated with positive outcomes across the CVD continuum but mat also have a role in the prevention or delay of diabetes (a major cardiovascular risk factor). Ongoing trials are aiming to define the place of such agents in lessening morbidity and mortality from CVD.
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