Publication

Clinical Translation of Nitrite Therapy for Cardiovascular Diseases

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Last modified
  • 02/20/2025
Type of Material
Authors
    John W Calvert, Emory UniversityDavid J. Lefer, Emory University
Language
  • English
Date
  • 2010-02-15
Publisher
  • Elsevier
Publication Version
Copyright Statement
  • © 2009 Elsevier Inc. All rights reserved.
License
Final Published Version (URL)
Title of Journal or Parent Work
ISSN
  • 1089-8603
Volume
  • 22
Issue
  • 2
Start Page
  • 91
End Page
  • 97
Grant/Funding Information
  • Supported by grants from the ADA (7-09-BS-26) to J.W.C. and by grants from the NIH (2RO1 HL-060849-09 and 5R01 HL-092141-01) to D.J.L., as well as funds from the Carlyle Fraser Heart Center of Emory University Hospital Midtown.
Abstract
  • The anion nitrite is an oxidative breakdown product of nitric oxide (NO) that has traditionally been viewed as a diagnostic marker of NO formation in biological systems. In this regard, nitrite has long been considered an inert oxidation product of NO metabolism. More recently, this view has changed with the discovery that nitrite represents a physiologically relevant storage reservoir of NO in blood and tissues that can readily be reduced to NO under pathological conditions. This has sparked a renewed interest in the biological role of nitrite and has led to an extensive amount of work investigating its therapeutic potential. As a result, nitrite therapy has now been shown to be cytoprotective in numerous animal models of disease. Given the very robust preclinical data regarding the cytoprotective effects of nitrite therapy it is very logical to consider the clinical translation of nitrite-based therapies. This article will review some of this preclinical data and will discuss the potential use of nitrite therapy as a therapeutic agent for the treatment of cardiovascular diseases including: ischemia-reperfusion injury (i.e. acute myocardial infarction and stroke), hypertension, angiogenesis, and as an adjunctive therapy for transplantation of various organs (i.e. liver and lung).
Author Notes
  • Correspondence: David J. Lefer, Ph.D., Department of Surgery, Emory University School of Medicine, Carlyle Fraser Heart Center, Emory University Hospital Midtown, 550 Peachtree Street NE, Atlanta, GA 30308-2247; Phone: (404) 686-1820; Fax: (404) 686-4884; Email: dlefer@emory.edu
Research Categories
  • Health Sciences, General
  • Health Sciences, Medicine and Surgery

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