Angiotensin II signaling and its implication in erectile dysfunction

J Sex Med. 2009 Mar:6 Suppl 3:302-10. doi: 10.1111/j.1743-6109.2008.01188.x.

Abstract

Introduction: Angiotensin II (Ang II) is the primary effector of the renin-angiotensin system (RAS). Ang II exerts its diverse physiologic actions via angiotensin type 1 and type 2 receptors. Recent evidence shows that tissue RAS exists in the penis, therefore indicating a significant role for Ang II in erectile function.

Aim: To summarize the recent findings on the importance of Ang II in normal erection physiology and the pathogenesis of erectile dysfunction (ED).

Methods: This article reviews the literature that relates to the role of RAS in the regulation of erectile function.

Main outcome measures: Evidence in the literature on the association between Ang II and the development of ED.

Results: Elevated Ang II levels contribute to the development of ED in humans and different animal models. Pharmacologic therapy interrupting RAS may be beneficial for patients with ED.

Conclusion: Studies have demonstrated that RAS is crucial in erectile function. Better understanding of the signaling pathways mediating Ang II physiologic actions will provide important information for the treatment of ED.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Aldosterone / biosynthesis
  • Angiotensin II / metabolism*
  • Animals
  • Disease Models, Animal
  • Endothelium, Vascular / enzymology
  • Erectile Dysfunction / enzymology
  • Erectile Dysfunction / metabolism*
  • Humans
  • Male
  • Muscle, Smooth / metabolism
  • Nitric Oxide Synthase / metabolism
  • Penis / blood supply
  • Penis / metabolism
  • Renin-Angiotensin System / physiology*
  • Signal Transduction / physiology*
  • Sympathetic Nervous System / metabolism
  • Vasoconstriction / physiology
  • Vasopressins / biosynthesis
  • rho-Associated Kinases / metabolism

Substances

  • Vasopressins
  • Angiotensin II
  • Aldosterone
  • Nitric Oxide Synthase
  • rho-Associated Kinases