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表面活性剂诱导的干性鳞屑皮肤中的角质层脂质异常。

Stratum corneum lipid abnormalities in surfactant-induced dry scaly skin.

作者信息

Fulmer A W, Kramer G J

出版信息

J Invest Dermatol. 1986 May;86(5):598-602. doi: 10.1111/1523-1747.ep12355351.

DOI:10.1111/1523-1747.ep12355351
PMID:3745969
Abstract

Sodium dodecyl sulfate (SDS) has been used to induce a dry scaly skin condition in human subjects. Measurements of stratum (s.) corneum hydration, scaliness, and lipid composition reveal in vivo surfactant perturbations on desquamation. Subjects (n = 10) were briefly treated daily with a 4% aqueous solution of SDS on one lower leg over a period of 2 weeks. The other control leg received no treatments. At the end of the treatment period, both lower legs were evaluated for hydration using an electrical impedance technique and examined by an independent dermatologist using a visually based grading scale for surface roughness and scaliness. Shave biopsies were then excised from each lower leg for analysis of s. corneum lipids. Treatment resulted in decreased s. corneum hydration and increased surface scale/roughness. These physical changes were accompanied by significant changes in s. corneum lipid composition. While surfactant treatments did not alter the total quantity of lipids per gram s. corneum protein, significant changes in specific lipid classes were observed. The free cholesterol to cholesterol ester ratio increased while the quantity of total sterols remained constant. The distribution of certain ceramide species were altered while the quantity of total ceramides remained constant. Free fatty acids were resolved into 2 distinct bands, only one of which diminished upon treatment. These results are interpreted in terms of a model for surfactant-induced perturbation of keratinization which leads to abnormal s. corneum lipids and altered desquamation.

摘要

十二烷基硫酸钠(SDS)已被用于在人体受试者中诱发皮肤干燥鳞屑状况。对角质层水合作用、鳞屑程度和脂质成分的测量揭示了体内表面活性剂对脱屑过程的干扰。10名受试者的一条小腿每天用4%的SDS水溶液进行短期处理,持续2周。另一条对照腿不接受任何处理。在治疗期结束时,使用电阻抗技术评估两条小腿的水合作用,并由一名独立的皮肤科医生使用基于视觉的分级量表检查表面粗糙度和鳞屑程度。然后从每条小腿上切取剃毛活检组织用于分析角质层脂质。治疗导致角质层水合作用降低,表面鳞屑/粗糙度增加。这些物理变化伴随着角质层脂质成分的显著变化。虽然表面活性剂处理并未改变每克角质层蛋白质中脂质的总量,但观察到特定脂质类别的显著变化。游离胆固醇与胆固醇酯的比例增加,而总甾醇的量保持不变。某些神经酰胺种类的分布发生改变,而总神经酰胺的量保持不变。游离脂肪酸被分离为两条不同的条带,处理后只有其中一条减少。这些结果根据表面活性剂诱导的角质化干扰模型进行解释,该模型导致角质层脂质异常和脱屑改变。

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