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The Renin-Angiotensin System and the Cerebrovascular Diseases: Experimental and Clinical Evidence
Lucas M Kangussu1, Lucas Alexandre Santos Marzano2, Cássio Ferraz Souza2
1Department of Morphology - Biological Science Institute, Federal University of Minas Gerais, Belo Horizonte, MG, Brazil.
Abstract:
Cerebrovascular Diseases (CVD) comprise a wide spectrum of disorders, all sharing an acquired or inherited alteration of the cerebral vasculature. CVD have been associated with important changes in systemic and tissue Renin-Angiotensin System (RAS). The aim of this review was to summarize and to discuss recent findings related to the modulation of RAS components in CVD. The role of RAS axes is more extensively studied in experimentally induced stroke. By means of AT1 receptors in the brain, Ang II hampers cerebral blood flow and causes tissue ischemia, inflammation, oxidative stress, cell damage and apoptosis. On the other hand, Ang-(1-7) by stimulating Mas receptor promotes angiogenesis in brain tissue, decreases oxidative stress, neuroinflammation, and improves cognition, cerebral blood flow, neuronal survival, learning and memory. In regard to clinical studies, treatment with Angiotensin Converting Enzyme (ACE) inhibitors and AT1 receptor antagonists exerts preventive and therapeutic effects on stroke. Besides stroke, studies support a similar role of RAS molecules also in traumatic brain injury and cerebral aneurysm. The literature supports a beneficial role for the alternative RAS axis in CVD. Further studies are necessary to investigate the therapeutic potential of ACE2 activators and/or Mas receptor agonists in patients with CVD.
Insights
The Renin-Angiotensin System (RAS) impacts cerebrovascular diseases (CVD). The Ang-(1-7) pathway shows therapeutic potential, unlike Ang II, offering new avenues for treating brain vascular conditions.
Area of Science:
- Neuroscience
- Cardiovascular Research
- Genetics
Background:
- Cerebrovascular diseases (CVD) involve alterations in cerebral vasculature.
- The Renin-Angiotensin System (RAS) plays a significant role in systemic and tissue changes associated with CVD.
Purpose of the Study:
- To review and discuss recent findings on RAS component modulation in CVD.
- To explore the dual role of RAS axes in experimental and clinical cerebrovascular conditions.
Main Methods:
- Literature review of experimental and clinical studies on RAS in CVD.
- Analysis of the effects of Angiotensin II (Ang II) and Angiotensin-(1-7) [Ang-(1-7)] on brain tissue.
- Examination of clinical data on Angiotensin Converting Enzyme (ACE) inhibitors and AT1 receptor antagonists.
Main Results:
- In experimental stroke, Ang II via AT1 receptors exacerbates ischemia, inflammation, and cell damage.
- Ang-(1-7) via Mas receptor promotes neuroprotection, angiogenesis, and cognitive benefits.
- Clinical studies show ACE inhibitors and AT1 antagonists have preventive and therapeutic effects on stroke.
Conclusions:
- The alternative RAS axis, particularly Ang-(1-7), demonstrates beneficial effects in CVD.
- Further research into ACE2 activators and Mas receptor agonists is warranted for CVD therapeutic development.
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