Literature DB >> 1748819

Low catalase levels in the epidermis of patients with vitiligo.

K U Schallreuter1, J M Wood, J Berger.   

Abstract

Suction blister roofs taken from the involved and uninvolved epidermis of patients with vitiligo showed a consistent reduction in levels of catalase compared to normal healthy controls of matched photo-skin types (Fitzpatrick classification). A decrease in catalase activity is expected to increase the concentration of hydrogen peroxide in the epidermis of these patients. Hydrogen peroxide functions as a reversible inhibitor of human tyrosinase with a KI of 8 X 10(-6) M. Also, hydrogen peroxide undergoes photochemical reduction yielding highly reactive hydroxyl radicals (OH.) and hydroxyl ions (OH-) mainly by the Haber-Weiss reaction. Hydroxyl radicals are capable of bleaching constitutional melanin and cause membrane lysis through lipid peroxidation reactions. Hydroxyl ions increase the pH in the epidermis, and as a consequence glutathione reductase activity is increased in patients with vitiligo compared to controls. Based on these new results, together with the previously reported calcium transport defect, a new hypothesis has been formulated for the pathogenesis of vitiligo.

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Year:  1991        PMID: 1748819     DOI: 10.1111/1523-1747.ep12492612

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


  42 in total

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

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7.  Increased in vitro expression of beta 2-adrenoceptors in differentiating lesional keratinocytes of vitiligo patients.

Authors:  K U Schallreuter; J M Wood; M R Pittelkow; N N Swanson; V Steinkraus
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8.  Comparison of plasma malondialdehyde, glutathione, glutathione peroxidase, hydroxyproline and selenium levels in patients with vitiligo and healthy controls.

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

Authors:  Akrem Jalel; Gaigi Siala Soumaya; Mohamed Hédi Hamdaoui
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10.  Oxidative stress in experimental vitiligo C57BL/6 mice.

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