Biomarkers of oxidative stress in epidermis of Tunisian pemphigus foliaceus patients
Background Reactive oxygen species play a key role in the development of many dermatological disorders. Objective The purpose of this study is to examine the lipid peroxidation, protein oxidation and antioxidative profile in Tunisian pemphigus foliaceus (PF) patients. Methods Malondialdehyde (MDA...
Gespeichert in:
Veröffentlicht in: | Journal of the European Academy of Dermatology and Venereology 2013-03, Vol.27 (3), p.e271-e275 |
---|---|
Hauptverfasser: | , , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
Zusammenfassung: | Background Reactive oxygen species play a key role in the development of many dermatological disorders.
Objective The purpose of this study is to examine the lipid peroxidation, protein oxidation and antioxidative profile in Tunisian pemphigus foliaceus (PF) patients.
Methods Malondialdehyde (MDA), conjugated dienes (CD), protein thiol levels, catalase (CAT) and superoxide dismutase (SOD) activities were evaluated in skin biopsies of 13 patients compared to biopsies of 7 healthy controls.
Results Oxidative stress was confirmed in these three types of patient biopsies as compared to controls. Thus, MDA, CD levels and catalase CAT and SOD activities were significantly increased in lesional, perilesional and normal biopsies of PF patients than in those of control subjects. Protein oxidative was confirmed by lower levels of protein thiols in lesional, perilesional and normal biopsies than in control’s biopsies. Otherwise, in patients, a significant rise of these biomarkers was observed in lesional and perilesional biopsies compared with normal biopsies.
Conclusion This study shows that oxidative stress could be involved in the pathogenesis of PF by the spread of skin lesions and/or by the increase in auto‐antibodies’ reactivity. |
---|---|
ISSN: | 0926-9959 1468-3083 |
DOI: | 10.1111/j.1468-3083.2012.04626.x |