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5-甲氧基补骨脂素对紫外线辐射诱导的人体皮肤DNA损伤的光化学保护作用的起效时间和持续时间。

The time of onset and duration of 5-methoxypsoralen photochemoprotection from UVR-induced DNA damage in human skin.

作者信息

Chadwick C A, Potten C S, Cohen A J, Young A R

机构信息

CRG Department of Epithelial Biology, Paterson Institute for Cancer Research, Christie Hospital (NHS) Trust, Manchester, U.K.

出版信息

Br J Dermatol. 1994 Oct;131(4):483-94. doi: 10.1111/j.1365-2133.1994.tb08548.x.

Abstract

Sites of previously unexposed buttock skin of eight human volunteers (skin type II) were treated daily for 3, 5, 8, or 10 days with suberythemogenic doses of solar-simulated radiation (SSR) in the presence of a UVB sunscreen containing 5-methoxypsoralen (5-MOP) at 30 p.p.m., or daily for 10 days with SSR+the same sunscreen without 5-MOP. One week after cessation of treatment, these sites, together with a control unexposed site, were challenged with 2 minimal erythema doses (2 MED) of SSR. Biopsy samples were taken within 15 min of the challenge dose, and were incubated for 1 h in tritiated thymidine. UV-induced DNA damage was measured indirectly by unscheduled DNA synthesis (UDS), and directly using a monoclonal antibody to thymine dimers, and automated image analysis. The level of pigmentation was assessed in sections in a semiquantiative fashion with Masson-Fontana staining, and the number of layers in the stratum corneum was used to assess changes in epidermal thickness. Using the UDS and dimer measurements, the level of photochemoprotection afforded by 5-MOP was determined from the reduction in the level of DNA damage observed. The photochemoprotection was expressed as a ratio of the 5-MOP-treated sites compared with the sites that did not receive 5-MOP treatment. The onset of 5-MOP photochemoprotection was shown to occur after three to five daily exposures, and became maximal after eight daily exposures. The onset of this protection coincided with increases in melanin and in stratum corneum thickness. In an extension of this study, it was found that following 10 daily exposures, 5-MOP photochemoprotection declined at a rate of about 5% per week, and in spite of several cycles of epidermal cell replacement, some protection still persisted up to 14 weeks after the end of the tanning protocol. The sites treated with sunscreen without 5-MOP was good correlation between the photochemoprotection endpoints of UDS and thymine dimer levels. The importance of 5-MOP photochemoprotection in the risk-benefit assessment of sunscreens used in suntanning is discussed.

摘要

八名人类志愿者(II型皮肤)先前未暴露的臀部皮肤部位,在含有30 ppm 5-甲氧基补骨脂素(5-MOP)的UVB防晒霜存在的情况下,每天用亚红斑剂量的太阳模拟辐射(SSR)处理3、5、8或10天,或者每天用SSR加不含5-MOP的相同防晒霜处理10天。治疗停止一周后,这些部位与一个未暴露的对照部位一起接受2个最小红斑剂量(2 MED)的SSR照射。在给予激发剂量后15分钟内采集活检样本,并在氚标记胸腺嘧啶核苷中孵育1小时。通过非计划DNA合成(UDS)间接测量紫外线诱导的DNA损伤,并直接使用抗胸腺嘧啶二聚体单克隆抗体和自动图像分析进行测量。用Masson-Fontana染色以半定量方式评估切片中的色素沉着水平,并用角质层的层数评估表皮厚度的变化。使用UDS和二聚体测量,根据观察到的DNA损伤水平的降低来确定5-MOP提供的光化学保护水平。光化学保护表示为5-MOP处理部位与未接受5-MOP处理部位的比率。结果表明,5-MOP光化学保护在每日暴露三至五次后开始出现,在每日暴露八次后达到最大值。这种保护的开始与黑色素和角质层厚度的增加同时发生。在本研究的扩展中,发现每日暴露10次后,5-MOP光化学保护以每周约5%的速率下降,并且尽管经历了几个表皮细胞更替周期,在晒黑方案结束后长达14周仍有一些保护作用持续存在。用不含5-MOP的防晒霜处理的部位,UDS和胸腺嘧啶二聚体水平的光化学保护终点之间具有良好的相关性。讨论了5-MOP光化学保护在晒黑用防晒霜风险效益评估中的重要性。

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