Human erythrocytes were subjected to oxidative stress using arsenicals. The study is a model for thiol-related redox processes observed in the etiology of diseases such as rheumatoid arthritis. Spin-echo NMR spectroscopy of the living cell was used to monitor the cellular biochemistry. Oxidation of
Stability and nonreactivity of ergothioneine in human erythrocytes studied by 1H NMR
β Scribed by Caroline D. Rae; Kimberley J. E. Sweeney; Philip W. Kuchel
- Publisher
- John Wiley and Sons
- Year
- 1993
- Tongue
- English
- Weight
- 340 KB
- Volume
- 29
- Category
- Article
- ISSN
- 0740-3194
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β¦ Synopsis
Abstract
The N(CH~3~)~3~ resonance of ergothioneine in ^1^H spinβecho Fourier transform (SEFT) NMR spectra of red blood cells is usually a large singlet and it has been common practice to use this apparently unchanging resonance as an intensity reference. Recently, Reglinski et al. (Magn. Reson. Med. 6, 217β223 (1988)) have questioned this practice, reporting changes seen in the resonance in response to oxidative stress induced by arsenicals. We propose that the changes in the ergothioneine resonance that were reported are artifacts due to alterations in osmolality and magnetic susceptibility induced by the addition of nonisotonic solutions to red blood cell suspensions. These factors change the specific intensity of the intracellular resonances of all compounds. Ergothioneine was observed not to take part in any chemical reactions with arsenicals in free solution or in intact erythrocytes, and we conclude that ergothioneine may still be used as an internal intensity reference in ^1^H SEFT NMR spectra, bearing in mind the above physical factors.
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