Angiotensin receptor blockers and angiogenesis: clinical and experimental evidence

Lauren M Willis1, Azza B El-Remessy, Payaningal R Somanath

  • 1Program in Clinical and Experimental Therapeutics, University of Georgia College of Pharmacy, Charlie Norwood VA Medical Center, Augusta, GA 30912, USA.

Insights

Angiotensin II receptor blockers (ARBs) show conflicting effects on blood vessel growth. This review examines ARB-induced angiogenesis in disease models, exploring mechanisms and clinical relevance.

Area of Science:

  • Cardiovascular Research
  • Oncology
  • Nephrology

Background:

  • Angiotensin II type 1 receptor antagonists (ARBs) are crucial for blood pressure management, renal, and cardiac protection, especially in patients intolerant to ACE inhibitors.
  • Conflicting evidence exists regarding ARBs' impact on angiogenesis, with some studies suggesting tumor promotion and others indicating beneficial vascular effects.

Purpose of the Study:

  • To review the angiogenic effects of ARBs in animal and cellular models of cardiovascular disease, stroke, and cancer.
  • To explore the molecular mechanisms underlying ARB-mediated angiogenesis.
  • To discuss the clinical implications of ARB use concerning vascular effects.

Main Methods:

  • Review of existing literature on ARBs and angiogenesis in various disease models.
  • Analysis of studies investigating molecular pathways involved in ARB-induced vascular changes.
  • Synthesis of findings to evaluate clinical consequences.

Main Results:

  • ARBs demonstrate predominantly anti-angiogenic effects in models of cancer and retinopathy.
  • Conversely, ARBs have shown pro-angiogenic effects in myocardial infarction and stroke models, improving vascular density and recovery.
  • Proposed mechanisms involve modulation of growth factors and signaling pathways.

Conclusions:

  • The angiogenic effects of ARBs are context-dependent, varying significantly across different disease models.
  • Understanding these dual effects is critical for optimizing ARB therapy and managing potential risks.
  • Further research is needed to fully elucidate the clinical impact of ARB-mediated angiogenesis.

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