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外用凯林与紫外线A或模拟阳光辐射联合治疗对轻度色素沉着的无毛小鼠具有致癌性。

Treatment with topical khellin in combination with ultraviolet A or solar-simulated radiation is carcinogenic to lightly pigmented hairless mice.

作者信息

Bech-Thomsen N, Wulf H C

机构信息

Department of Dermatology, National University Hospital, Rigshospitalet, Copenhagen, Denmark.

出版信息

Photodermatol Photoimmunol Photomed. 1995 Oct-Dec;11(5-6):204-8. doi: 10.1111/j.1600-0781.1995.tb00170.x.

Abstract

Khellin is used together with either UVA irradiation or sun exposure in the treatment of vitiligo. The purpose of this study was to investigate the carcinogenic effect of topically applied khellin together with UVA or solar simulated radiation (SSR) in lightly pigmented C3H/Tif mice. For comparison purposes a 0.1% 8-methoxypsoralen (8-MOP) cream was also tested in combination with SSR. Fifty microliters of a 5% khellin cream, a 0.1% 8-MOP cream, or a cream without active substances were spread uniformly on the back of the mice 30 minutes before UVA or SSR irradiation. All mice were irradiated 3 times a week until age or skin tumor development necessitated killing. Treatment with topical khellin and UVA irradiation was carcinogenic to lightly pigmented hairless mice, time to 50% of the mice had developed one tumor (t50) was 507 days. This indicates that the combination of topical khellin and UVA radiation, formerly expected to be rather innocuous, is carcinogenic to mice. Also the combination of khellin and SSR (t50 = 268 days) enhanced skin tumor development significantly compared with control cream and SSR (t50 = 330 days), P < 0.05. In addition, the combination of khellin and SSR was found to have the same carcinogenic effect as treatment with 0.1% 8-MOP and SSR (t50 = 262 days). This study shows that topically applied khellin increases the carcinogenic effect of both UVA and sunlight.

摘要

凯林与紫外线A(UVA)照射或阳光照射联合用于白癜风的治疗。本研究的目的是调查在色素较浅的C3H/Tif小鼠中局部应用凯林与UVA或模拟太阳辐射(SSR)联合使用的致癌作用。为了进行比较,还测试了0.1%的8-甲氧基补骨脂素(8-MOP)乳膏与SSR联合使用的情况。在UVA或SSR照射前30分钟,将50微升5%的凯林乳膏、0.1%的8-MOP乳膏或无活性物质的乳膏均匀涂抹在小鼠背部。所有小鼠每周照射3次,直到因年龄或皮肤肿瘤发展需要处死。局部应用凯林和UVA照射对色素较浅的无毛小鼠具有致癌性,50%的小鼠出现一个肿瘤的时间(t50)为507天。这表明局部应用凯林和UVA辐射,以前认为相当无害,对小鼠具有致癌性。与对照乳膏和SSR(t50 = 330天)相比,凯林和SSR联合使用(t50 = 268天)也显著促进了皮肤肿瘤的发展,P < 0.05。此外,发现凯林和SSR联合使用与0.1%的8-MOP和SSR治疗具有相同的致癌作用(t50 = 262天)。本研究表明,局部应用凯林会增加UVA和阳光的致癌作用。

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