用人体重建表皮评价化合物和外用成品的光毒性潜能。

J. Medina, C. Elsaesser, V. Picarles, O. Grenet, M. Kolopp, S. Chibout, A. de Brugerolle de Fraissinette
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引用次数: 21

摘要

本研究的目的是设计一个模型系统,通过测试一些具有代表性的光毒性(P)和非光毒性(NP)化合物和成品外用产品,利用人重建表皮(HRE, skininetic Laboratories, Nice, France)来评估光毒性潜能。在UVA光存在和不存在的情况下,对5-5000微克/毫升试验剂应用24小时的组织反应进行了分析,包括活力(乳酸脱氢酶释放)、促炎活性(IL-8释放和mRNA表达)和形态学(组织病理学)。8-甲氧补骨脂素(P)和异丙嗪(P)产生的细胞毒浓度-反应曲线在辐照组织和非辐照组织之间有显著差异,而十二烷基硫酸钠(NP)则没有。仅辐照组织出现形态学损伤。在培养基中应用四环素(P),但不是局部应用,也会引起类似的光毒性迹象。6-甲基coumarine(弱P)没有细胞毒性,但仅在UVA照射后才增加IL-8的释放和mRNA的表达。含有1% 8-甲氧基补骨脂素(P)或煤焦油(P)的PUVA治疗霜降低了暴露于uva的组织的活力并诱导了组织学损伤。总之,通过使用分层策略,包括确定细胞毒性、IL-8的产生和HRE暴露于化合物和UVA光后的形态学损伤,正确预测了所测试试剂的光毒性潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Assessment of the phototoxic potential of compounds and finished topical products using a human reconstructed epidermis.
The goal of this study was to design a model system for the assessment of phototoxic potential using a human reconstructed epidermis (HRE, SkinEthic Laboratories, Nice, France), by testing some representative phototoxic (P) and non-phototoxic (NP) compounds and finished topical products. The tissue response to 24-h application of 5-5000 microg/mL of the test agents in the presence and absence of UVA light was analyzed in terms of viability (Lactate Dehydrogenase release), pro-inflammatory activity (IL-8 release and mRNA expression) and morphology (histopathology). 8-Methoxypsoralen (P) and promethazin (P), but not sodium lauryl sulfate (NP) produced cytotoxicity concentration-response curves significantly different between irradiated and nonirradiated tissues. Only irradiated tissues showed morphological damage. Application of tetracyclin (P) in the culture medium, but not topically, induced similar signs of phototoxicity. 6-Methylcoumarine (weak P) was not cytotoxic, yet it increased IL-8 release and mRNA expression only following UVA irradiation. PUVA therapy creams containing 1% 8-Methoxy-psoralen (P) or coal tar (P) decreased viability and induced histologic damage in UVA-exposed tissues. In conclusion, the phototoxic potential of the tested agents was correctly predicted by using a tiered strategy that involves determining cytotoxicity, production of IL-8, and morphological damage following exposure of the HRE to the compounds and UVA light.
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