Literature DB >> 12855429

Orthogonal properties of the redox siblings nitroxyl and nitric oxide in the cardiovascular system: a novel redox paradigm.

David A Wink1, Katrina M Miranda, Tatsuo Katori, Daniele Mancardi, Douglas D Thomas, Lisa Ridnour, Michael G Espey, Martin Feelisch, Carol A Colton, Jon M Fukuto, Pasquale Pagliaro, David A Kass, Nazareno Paolocci.   

Abstract

Endogenous formation of nitric oxide (NO) and related nitrogen oxides in the vascular system is critical to regulation of multiple physiological functions. An imbalance in the production or availability of these species can result in progression of disease. Nitrogen oxide research in the cardiovascular system has primarily focused on the effects of NO and higher oxidation products. However, nitroxyl (HNO), the one-electron-reduction product of NO, has recently been shown to have unique and potentially beneficial pharmacological properties. HNO and NO often induce discrete biological responses, providing an interesting redox system. This article discusses the emerging aspects of HNO chemistry and attempts to provide a framework for the distinct effects of NO and HNO in vivo.

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Year:  2003        PMID: 12855429     DOI: 10.1152/ajpheart.00531.2003

Source DB:  PubMed          Journal:  Am J Physiol Heart Circ Physiol        ISSN: 0363-6135            Impact factor:   4.733


  27 in total

1.  Mechanisms of the interaction of nitroxyl with mitochondria.

Authors:  Sruti Shiva; Jack H Crawford; Anup Ramachandran; Erin K Ceaser; Tess Hillson; Paul S Brookes; Rakesh P Patel; Victor M Darley-Usmar
Journal:  Biochem J       Date:  2004-04-15       Impact factor: 3.857

Review 2.  The pharmacology of nitroxyl (HNO) and its therapeutic potential: not just the Janus face of NO.

Authors:  Nazareno Paolocci; Matthew I Jackson; Brenda E Lopez; Katrina Miranda; Carlo G Tocchetti; David A Wink; Adrian J Hobbs; Jon M Fukuto
Journal:  Pharmacol Ther       Date:  2006-11-29       Impact factor: 12.310

Review 3.  The emergence of nitroxyl (HNO) as a pharmacological agent.

Authors:  Christopher H Switzer; Wilmarie Flores-Santana; Daniele Mancardi; Sonia Donzelli; Debashree Basudhar; Lisa A Ridnour; Katrina M Miranda; Jon M Fukuto; Nazareno Paolocci; David A Wink
Journal:  Biochim Biophys Acta       Date:  2009-05-06

4.  The shy Angeli and his elusive creature: the HNO route to vasodilation.

Authors:  Nazareno Paolocci; David A Wink
Journal:  Am J Physiol Heart Circ Physiol       Date:  2009-03-13       Impact factor: 4.733

5.  Direct detection of nitroxyl in aqueous solution using a tripodal copper(II) BODIPY complex.

Authors:  Joel Rosenthal; Stephen J Lippard
Journal:  J Am Chem Soc       Date:  2010-04-28       Impact factor: 15.419

Review 6.  The specificity of nitroxyl chemistry is unique among nitrogen oxides in biological systems.

Authors:  Wilmarie Flores-Santana; Debra J Salmon; Sonia Donzelli; Christopher H Switzer; Debashree Basudhar; Lisa Ridnour; Robert Cheng; Sharon A Glynn; Nazareno Paolocci; Jon M Fukuto; Katrina M Miranda; David A Wink
Journal:  Antioxid Redox Signal       Date:  2011-03-16       Impact factor: 8.401

Review 7.  Redox signaling and protein phosphorylation in mitochondria: progress and prospects.

Authors:  D Brian Foster; Jennifer E Van Eyk; Eduardo Marbán; Brian O'Rourke
Journal:  J Bioenerg Biomembr       Date:  2009-04       Impact factor: 2.945

8.  Dual mechanisms of HNO generation by a nitroxyl prodrug of the diazeniumdiolate (NONOate) class.

Authors:  Daniela Andrei; Debra J Salmon; Sonia Donzelli; Azadeh Wahab; John R Klose; Michael L Citro; Joseph E Saavedra; David A Wink; Katrina M Miranda; Larry K Keefer
Journal:  J Am Chem Soc       Date:  2010-10-29       Impact factor: 15.419

Review 9.  Physiological and pharmacological features of the novel gasotransmitter: hydrogen sulfide.

Authors:  Daniele Mancardi; Claudia Penna; Annalisa Merlino; Piero Del Soldato; David A Wink; Pasquale Pagliaro
Journal:  Biochim Biophys Acta       Date:  2009-03-13

10.  Photoinduced release of nitroxyl and nitric oxide from diazeniumdiolates.

Authors:  Sergei V Lymar; Vladimir Shafirovich
Journal:  J Phys Chem B       Date:  2007-05-08       Impact factor: 2.991

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