Bioassay discrimination between nitric oxide (NO) and nitroxyl (NO-) using L-cysteine

Pino, R.Z. and Feelisch, M. (1994) Bioassay discrimination between nitric oxide (NO) and nitroxyl (NO-) using L-cysteine. Biochemical and Biophysical Research Communications, 201, (1), 54-62. (doi:10.1006/bbrc.1994.1668). (PMID:8198612).


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Nitroxyl (NO-) is the one-electron reduction product of nitric oxide (NO.). Recently, NO- generating compounds were shown to possess potent vasorelaxant activity and this was attributed to the ready conversion of NO- to NO.. Because of its metastable character, direct chemical detection of NO- or its conjugated acid, HNO, has not been accomplished yet. In order to gain further insight into the cellular mode of action of NO- generating compounds we aimed at finding a means to discriminate NO- from NO. by bioassay. Using isolated rat aortic rings in organ baths, we here show that high concentrations of L-cysteine cause complete inhibition of the vasorelaxant response to NO- (generated from Angeli's salt and sodium nitroxyl) whereas responses to authentic NO. and S-nitrosocysteine are largely enhanced. Preliminary results indicate that the inhibition by L-cysteine of NO- activity may be mediated in part by enzymatic and non-enzymatic mechanisms. Whether or not NO- generating compounds will have promising therapeutic potential as a new class of NO.- donors will not least depend on their interference with enzymatic routes susceptible to inhibition by NO-.

Item Type: Article
Digital Object Identifier (DOI): doi:10.1006/bbrc.1994.1668
ISSNs: 0006-291X (print)
1090-2104 (electronic)
Subjects: R Medicine > R Medicine (General)
Divisions : Faculty of Medicine > Clinical and Experimental Sciences
ePrint ID: 337906
Accepted Date and Publication Date:
30 May 1994Published
Date Deposited: 15 Aug 2012 10:22
Last Modified: 31 Mar 2016 14:27

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