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SLS-irritated human skin shows no correlation between degree of proliferation and TEWL increase
Authors:J. Welzel  Claudia Metker  Helmut H. Wolff  Klaus-Peter Wilhelm
Affiliation:Klinik für Dermatologie und Venerologie, Medizinische Universit?t zu Lübeck, Ratzeburger Allee 160, D-23538 Lübeck, Germany Tel.: +49-451-500 2515; Fax: +49-451-500 2981, DE
proDERM, Industriestra?e 1, 22869 Schenefeld/Hamburg, Germany, DE
Abstract:Abstract It is well known that cutaneous irritants influence epidermal proliferation but the pathogenesis is poorly understood. Recent investigations have shown that the skin barrier integrity influences the proliferation of the basal keratinocytes. Our question was whether the proliferating activity of keratinocytes is indeed regulated by the degree of skin barrier damage or by a direct toxic action of the irritant on the keratinocytes. Therefore various degrees of skin irritation were induced by the application of 0.1%, 0.5% and 2% sodium lauryl sulphate (SLS) solution to the forearm skin of six healthy volunteers. This experiment was performed to evaluate the relationship between SLS concentration and epidermal proliferation. In a second experiment another 14 volunteers were treated with a single SLS concentration (0.5%) to look for interindividual differences in the patterns of skin reaction and susceptibility to the irritant. Skin barrier function was evaluated by measurements of transepidermal water loss (TEWL) before and after irritation. Punch biopsies were taken after 96 h from exposed areas and from unexposed normal skin. Dividing keratinocytes were identified immunocytochemically using three different monoclonal antibodies: PCNA, MIB 1 and KiS1. Exposure to SLS resulted in concentration-dependent increases in both TEWL and epidermal proliferation. However, no significant correlation could be found between the degree of hyperproliferation and the TEWL changes. The results suggest that epidermal proliferation is modulated by a direct interaction of the surfactant with the keratinocytes and/or by release of mediators rather than the consequence of a barrier disturbance. Received: 5 February 1997 / Received after revision: 12 August 1998 / Accepted: 24 August 1998
Keywords:Skin barrier function  Proliferation  Sodium lauryl sulphate  Keratinocytes  Transepidermal  water loss
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