Literature DB >> 12395182

Sulphoacetaldehyde as a product of taurine chloramine peroxidation at site of inflammation.

S Olszowski1, E Olszowska, D Kusior, E Szneler.   

Abstract

It has been reported, that sulphoacetalhehyde is formed in the fagocytozing PMNs and its production is taurine monochloramine mediated. Since H(2)O(2) and secreted MPO are present in the medium the non- and enzymatic peroxidation of taurine of its mono- and dichloramines were examined within the pH range 5.3-7.4. The formation of sulphoacetaldehyde was observed in nonenzymatic hydrolysis of taurine N,N-dichloramine (pH 5.3) as well as for monochloramine at pH 7.4. It was found also that its formation was accelerated in the presence of H(2)O(2), in the MPO/H(2)O(2) and in the full system containing Cl(-). Additionally it was shown that also horseradish peroxidase (HRP) could catalyze sulphoacetaldehyde production. The sulphoacetaldehyde formation in the examined systems was confirmed with the use of (1)HNMR spectra of separated 2,4-dinitrophenylhydrazone derivative. Our results suggest that both non- and ezymatic processes could contribute to the sulphoacetaldehyde formation at site of inflammation.

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Year:  2002        PMID: 12395182     DOI: 10.1007/s007260200003

Source DB:  PubMed          Journal:  Amino Acids        ISSN: 0939-4451            Impact factor:   3.520


  1 in total

1.  Chemical characterization and biological properties of NVC-422, a novel, stable N-chlorotaurine analog.

Authors:  Lu Wang; Barbara Belisle; Mansour Bassiri; Ping Xu; Dmitri Debabov; Chris Celeri; Nichole Alvarez; Martin C Robson; Wyatt G Payne; Ramin Najafi; Behzad Khosrovi
Journal:  Antimicrob Agents Chemother       Date:  2011-03-21       Impact factor: 5.191

  1 in total

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