Determination of oxidative stress in vitiligo by measuring superoxide dismutase and catalase levels in vitiliginous and non-vitiliginous skin
Background: Vitiligo is an acquired disorder characterized by circumscribed depigmented macules devoid of identifiable melanocytes. Complex genetic, immunological, neural and self destructive mechanisms interplay in its pathogenesis. According to autocytotoxic hypothesis, oxidative stress has been s...
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Veröffentlicht in: | Indian journal of dermatology, venereology, and leprology venereology, and leprology, 2009-05, Vol.75 (3), p.268-271 |
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Zusammenfassung: | Background: Vitiligo is an acquired disorder characterized by
circumscribed depigmented macules devoid of identifiable melanocytes.
Complex genetic, immunological, neural and self destructive mechanisms
interplay in its pathogenesis. According to autocytotoxic hypothesis,
oxidative stress has been suggested to be the initial pathogenic event
in melanocyte degeneration. Aims: The aim of our investigation was to
evaluate the role of oxidative stress by measuring levels of the
antioxidant enzymes superoxide dismutase (SOD) and catalase (CAT) in
lesional and normal skin of patients with vitiligo and in the skin of
normal controls. Methods: We determined the activity of SOD in lesional
and non-lesional skin and CAT in lesional skin only of 25 vitiligo
patients and 25 controls by using the spectrophotometric assay and
Aebi′s method, respectively. Results: There was statistically
significant increase in the levels of SOD in vitiliginous and non
vitiliginous skin of patient group compared to the control group ( P
< 0.001). No significant difference was found between the levels of
SOD in lesional skin and non-lesional skin of vitiligo patients. The
levels of CAT in the skin of patients were found to be significantly
lower than those of controls ( P < 0.001). Conclusions: There is
increased oxidative stress in vitiligo as is indicated by high levels
of SOD and low levels of CAT in the skin of vitiligo patients. |
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ISSN: | 0378-6323 0973-3922 1998-3611 |
DOI: | 10.4103/0378-6323.48427 |