Literature DB >> 9284096

Increased sensitivity to peroxidative agents as a possible pathogenic factor of melanocyte damage in vitiligo.

V Maresca1, M Roccella, F Roccella, E Camera, G Del Porto, S Passi, P Grammatico, M Picardo.   

Abstract

To examine the sensitivity of vitiligo melanocytes to external oxidative stress, we studied enzymatic and non-enzymatic anti-oxidants in cultured melanocytes of normal subjects (n = 20) and melanocytes from apparently normal skin of vitiligo patients (n = 10). The activity of superoxide dismutase and catalase and the intracellular concentrations of vitamin E and ubiquinone were evaluated in cultures at the fourth or fifth passage. In addition, cells were exposed to various concentrations of a peroxidizing agent, cumene hydroperoxide (CUH, 0.66-20 microM), for 1 and 24 h. Compared to normal melanocytes, vitiligo melanocytes showed normal superoxide dismutase and significantly lower catalase activities and higher vitamin E and lower ubiquinone levels. At the concentration used, CUH did not significantly affect cell number or viability of melanocytes after either period of culture. On the contrary, vitiligo melanocytes were susceptible to the toxic effect of CUH after 24 h of continuous treatment at concentrations greater than 6.6 microM. The degree of CUH toxicity correlated strictly with the anti-oxidant pattern, defined as the ratio between vitamin E concentration and catalase activity, suggesting that the alteration in the antioxidants was the basis for sensitivity to the external oxidative stress. Our results demonstrate the presence of an imbalance in the anti-oxidant system in vitiligo melanocytes and provide further support for a free radical-mediated damage as an initial pathogenic event in melanocyte degeneration in vitiligo.

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Year:  1997        PMID: 9284096     DOI: 10.1111/1523-1747.ep12335801

Source DB:  PubMed          Journal:  J Invest Dermatol        ISSN: 0022-202X            Impact factor:   8.551


  43 in total

1.  Oxidative stress-induced overexpression of miR-25: the mechanism underlying the degeneration of melanocytes in vitiligo.

Authors:  Q Shi; W Zhang; S Guo; Z Jian; S Li; K Li; R Ge; W Dai; G Wang; T Gao; C Li
Journal:  Cell Death Differ       Date:  2015-08-28       Impact factor: 15.828

Review 2.  Vitiligo: Focus on Clinical Aspects, Immunopathogenesis, and Therapy.

Authors:  Katia Boniface; Julien Seneschal; Mauro Picardo; Alain Taïeb
Journal:  Clin Rev Allergy Immunol       Date:  2018-02       Impact factor: 8.667

3.  Promoter polymorphism -119C/G in MYG1 (C12orf10) gene is related to vitiligo susceptibility and Arg4Gln affects mitochondrial entrance of Myg1.

Authors:  Mari-Anne Philips; Külli Kingo; Maire Karelson; Ranno Rätsep; Eerik Aunin; Ene Reimann; Paula Reemann; Orm Porosaar; Jonas Vikeså; Finn C Nielsen; Eero Vasar; Helgi Silm; Sulev Kõks
Journal:  BMC Med Genet       Date:  2010-04-08       Impact factor: 2.103

4.  Oxidative stress level and tyrosinase activity in vitiligo patients.

Authors:  M Eskandani; J Golchai; N Pirooznia; S Hasannia
Journal:  Indian J Dermatol       Date:  2010       Impact factor: 1.494

5.  Transcriptional Analysis of Vitiligo Skin Reveals the Alteration of WNT Pathway: A Promising Target for Repigmenting Vitiligo Patients.

Authors:  Claire Regazzetti; Florence Joly; Carine Marty; Michel Rivier; Bruno Mehul; Pascale Reiniche; Carine Mounier; Yves Rival; David Piwnica; Marine Cavalié; Bérengère Chignon-Sicard; Robert Ballotti; Johannes Voegel; Thierry Passeron
Journal:  J Invest Dermatol       Date:  2015-08-31       Impact factor: 8.551

Review 6.  Innate immune mechanisms in vitiligo: danger from within.

Authors:  Jillian M Richmond; Michael L Frisoli; John E Harris
Journal:  Curr Opin Immunol       Date:  2013-11-12       Impact factor: 7.486

7.  Comparison of plasma malondialdehyde, glutathione, glutathione peroxidase, hydroxyproline and selenium levels in patients with vitiligo and healthy controls.

Authors:  I Cetin Ozturk; Kadir Batcioglu; Fikret Karatas; Ersoy Hazneci; Metin Genc
Journal:  Indian J Dermatol       Date:  2008       Impact factor: 1.494

8.  Vitiligo treatment with vitamins, minerals and polyphenol supplementation.

Authors:  Akrem Jalel; Gaigi Siala Soumaya; Mohamed Hédi Hamdaoui
Journal:  Indian J Dermatol       Date:  2009       Impact factor: 1.494

9.  Oxidative stress in experimental vitiligo C57BL/6 mice.

Authors:  Akrem Jalel; Mrabet Yassine; Mohamed Hédi Hamdaoui
Journal:  Indian J Dermatol       Date:  2009-07       Impact factor: 1.494

10.  Study of total antioxidant status and glutathione peroxidase activity in Tunisian vitiligo patients.

Authors:  Akrem Jalel; Mohamed Hédi Hamdaoui
Journal:  Indian J Dermatol       Date:  2009       Impact factor: 1.494

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