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222nm 紫外线 C 灭菌灯对紫外线敏感小鼠的长期影响。

Long-term Effects of 222-nm ultraviolet radiation C Sterilizing Lamps on Mice Susceptible to Ultraviolet Radiation.

机构信息

Division of Dermatology, Department of Internal Related, Graduate School of Medicine, Kobe University, Kobe, Japan.

Department of Ophthalmology, Faculty of Medicine, Shimane University, Izumo, Japan.

出版信息

Photochem Photobiol. 2020 Jul;96(4):853-862. doi: 10.1111/php.13269. Epub 2020 May 31.

DOI:10.1111/php.13269
PMID:32222977
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7497027/
Abstract

Germicidal lamps that emit primarily 254 nm ultraviolet radiation (UV) are routinely utilized for surface sterilization but cannot be used for human skin because they cause genotoxicity. As an alternative, 222-nm UVC has been reported to exert sterilizing ability comparable to that of 254-nm UVC without producing cyclobutane pyrimidine dimers (CPDs), the major DNA lesions caused by UV. However, there has been no clear evidence for safety in chronic exposure to skin, particularly with respect to carcinogenesis. We therefore investigated the long-term effects of 222-nm UVC on skin using a highly photocarcinogenic phenotype mice that lack xeroderma pigmentosum complementation group A (Xpa-) gene, which is involved in repairing of CPDs. CPDs formation was recognized only uppermost layer of epidermis even with high dose of 222-nm UVC exposure. No tumors were observed in Xpa-knockout mice and wild-type mice by repetitive irradiation with 222-nm UVC, using a protocol which had shown to produce tumor in Xpa-knockout mice irradiated with broad-band UVB. Furthermore, erythema and ear swelling were not observed in both genotype mice following 222-nm UVC exposure. Our data suggest that 222-nm UVC lamps can be safely used for sterilizing human skin as far as the perspective of skin cancer development.

摘要

杀菌灯主要发射 254nm 紫外线(UV),常用于表面消毒,但不能用于人体皮肤,因为它们会引起遗传毒性。作为替代方案,据报道,222nm UVC 具有与 254nm UVC 相当的杀菌能力,而不会产生由 UV 引起的主要 DNA 损伤——环丁烷嘧啶二聚体(CPD)。然而,对于皮肤的慢性暴露,特别是致癌性,还没有明确的安全性证据。因此,我们使用缺乏 Xeroderma Pigmentosum 互补组 A(Xpa-)基因的高度光致癌表型小鼠,研究了 222nm UVC 对皮肤的长期影响,Xpa 基因参与 CPD 的修复。即使在高剂量的 222nm UVC 照射下,也只能在上层表皮中识别到 CPDs 的形成。在使用已证明会导致 Xpa 敲除小鼠接受广谱 UVB 照射产生肿瘤的方案对 Xpa 敲除小鼠和野生型小鼠进行重复 222nm UVC 照射后,未观察到肿瘤。此外,在接受 222nm UVC 照射后,两种基因型的小鼠均未出现红斑和耳肿胀。我们的数据表明,只要从皮肤癌发展的角度来看,222nm UVC 灯就可以安全地用于消毒人体皮肤。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d7e/7497027/fb5f70c3857c/PHP-96-853-g007.jpg
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