Xenobiotic metabolism in human skin and 3D human skin reconstructs: A review

被引:42
作者
Gibbs, Sue
van de Sandt, Johannes J. M.
Merk, Hans F.
Lockley, David J.
Pendlington, Ruth U.
Pease, Camilla K.
机构
[1] Unilever, Safety & Environm Assurance Ctr, Sharnbrook MK44 1LQ, Beds, England
[2] Vrije Univ Amsterdam Med Ctr, Dept Dermatol, Amsterdam, Netherlands
[3] TNO, NL-3704 HE Zeist, Netherlands
[4] Rhein Westfal TH Aachen Klinikum, Univ Hosp, Dept Dermatol & Allergol, D-52074 Aachen, Germany
关键词
D O I
10.2174/138920007782798225
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
In this review, we discuss and compare studies of xenobiotic metabolism in both human skin and 3D human skill reconstructs. In comparison to the liver, the skin is a less studied organ in terms of characterising metabolic capability. While the skill forms the major protective barrier to environmental chemical exposure, it is also a potential target organ for adverse health effects. Occupational, accidental or intended-use exposure to toxic chemicals could result in acute or delayed injury to the skill (e.g. inflammation, allergy, cancer). Skin metabolism may play a role in the manifestation or amelioration ofadverse effects via the topical route. Today, we have robust testing strategies to assess the potential for local skin toxicity of chemical exposure. Such methods (e.g. the local lymph node assay for assessing skin sensitisation; skin painting carcinogenicity studies) incorporate skill metabolism implicitly in the in vivo model system used. In light of recent European legislation (i.e. 7(th) Amendment to the Cosmetics Directive and Registration Evaluation and Authorisation of existing Chemicals (REACH)), non-animal approaches will be required to reduce and replace animal experiments for chemical risk assessment. It is expected that new models and approaches will need to account for skill metabolism explicitly, as the mechanisms ofadverse effects in the skin are deconvoluted. 3D skin models have been proposed as a tool to use in new in vitro alternative approaches. In order to be able to use 3D skin models in this context, we need to understand their metabolic competency in relation to xenobiotic biotransformation and whether functional activity is representative of that seen in human skin.
引用
收藏
页码:758 / 772
页数:15
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