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Tyrosinase-mediated formation of a reactive quinone from the depigmenting agents, 4-tert-butylphenol and 4-tert-butylcatechol

Author:
  • K Thorneby-Andersson
  • Olov Sterner
  • Christer Hansson
Publishing year: 2000
Language: English
Pages: 33-38
Publication/Series: Pigment Cell Research1987-01-01+01:002008-01-01+01:00
Volume: 13
Issue: 1
Document type: Journal article
Publisher: Wiley-Blackwell

Abstract english

Exposure of the skin to certain phenols or catechols such as 4-tert-butylphenol (TBP) and 4-tert-butylcatechol (TBC) may cause leukoderma. These substances are used in the polymer industry and numerous cases have been reported. Several theories of the mechanism for chemical leukoderma have been suggested. In the present study, TBP and TBC are shown to be oxidised by tyrosinase. The oxidation of TBC yields a quinone that is further investigated on its reactions with cysteine or glutathione (GSH). The products formed are isolated and identified by mass spectrometry and nuclear magnetic resonance as being 4-tert-butyl-6-S-cysteinylcatechol (cys-TBC) and 4-tert-butyl-6-S-glutathionylcatechol (GS-TBC). The reactive quinone is a strongly electrophilic substance that rapidly reacts with GSH. A depletion of the GSH defence system may give conditions where the quinone lives long enough to effect its toxic properties. The influence of the reactive tert-butylquinone on enzymatic activities is demonstrated by the inhibition of glyceraldehyde-3-phosphate dehydrogenase.

Keywords

  • Dermatology and Venereal Diseases
  • Chemical leukoderma
  • Glutathione
  • Melanocyte
  • Pigmentation
  • Quinone

Other

Published
  • ISSN: 0893-5785
Olov Sterner
E-mail: olov [dot] sterner [at] science [dot] lu [dot] se

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