Nitric Oxide and Hydrogen Sulfide Regulation of Ischemic Vascular Remodeling

Microcirculation. 2016 Feb;23(2):134-45. doi: 10.1111/micc.12248.

Abstract

Blockage or restriction of blood flow through conduit arteries results in tissue ischemia downstream of the disturbed area. Local tissues can adapt to this challenge by stimulating vascular remodeling through angiogenesis and arteriogenesis thereby restoring blood perfusion and removal of wastes. Multiple molecular mechanisms of vascular remodeling during ischemia have been identified and extensively studied. However, therapeutic benefits from these findings and insights are limited due to the complexity of various signaling networks and a lack of understanding central metabolic regulators governing these responses. The gasotransmitters NO and H2 S have emerged as master regulators that influence multiple molecular targets necessary for ischemic vascular remodeling. In this review, we discuss how NO and H2 S are individually regulated under ischemia, what their roles are in angiogenesis and arteriogenesis, and how their interaction controls ischemic vascular remodeling.

Keywords: blood flow; endothelium; hypoxia; ischemia; oxygen.

Publication types

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

MeSH terms

  • Animals
  • Humans
  • Hydrogen Sulfide / metabolism*
  • Ischemia / metabolism*
  • Ischemia / pathology
  • Ischemia / therapy
  • Neovascularization, Pathologic / metabolism*
  • Neovascularization, Pathologic / pathology
  • Neovascularization, Pathologic / therapy
  • Nitric Oxide / metabolism*
  • Vascular Remodeling*

Substances

  • Nitric Oxide
  • Hydrogen Sulfide