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口服类胡萝卜素能否保护人类皮肤免受紫外线红斑、补骨脂素光毒性和紫外线诱导的DNA损伤?

Do oral carotenoids protect human skin against ultraviolet erythema, psoralen phototoxicity, and ultraviolet-induced DNA damage?

作者信息

Wolf C, Steiner A, Hönigsmann H

机构信息

Department of Dermatology I, University of Vienna, Austria.

出版信息

J Invest Dermatol. 1988 Jan;90(1):55-7. doi: 10.1111/1523-1747.ep12462564.

DOI:10.1111/1523-1747.ep12462564
PMID:3335790
Abstract

This study was performed in order to (1) assess the magnitude of a possible protective effect of oral carotenoids on ultraviolet B (UVB)-, ultraviolet A (UVA)-, and psoralen ultraviolet A (PUVA)-induced erythema in human skin and (2) to evaluate whether the postulated prevention of skin cancer by prophylactic administration of carotenoids is based on a decrease in UVB-induced DNA damage. Twenty-three healthy volunteers received oral carotenoids (150 mg/day) for 4 weeks. Serum levels were quantitated, and ranged from 390 to 1710 micrograms/dl. Before and after carotenoid administration, the UVA- and UVB-MEDs and the PUVA-MPD were determined by standard phototesting. DNA damage was assessed by autoradiographical measurement of unscheduled DNA synthesis (UDS) following UVB exposure before and after treatment. No statistically significant carotenoid-dependent protection was found against UVA, UVB, and PUVA erythema by comparing the pre- and postcarotenoid erythema doses. Also at the DNA level there was no indication of a protective effect that could be detected with the methods employed: the amount of UVB-induced UDS was not decreased after carotenoid treatment. We conclude that (1) carotenoids do not reduce UVB-, UVA-, or PUVA-induced erythema in human skin; that (2) reactive oxygen species may not be involved in PUVA-erythema production or, alternatively, carotenoids may not quench these radicals sufficiently in vivo; and that (3) carotenoid protection against UVB-induced carcinogenesis does not operate by reducing the number of mutagenic lesions in DNA.

摘要

进行本研究的目的是

(1)评估口服类胡萝卜素对人皮肤中紫外线B(UVB)、紫外线A(UVA)和补骨脂素紫外线A(PUVA)诱导的红斑可能具有的保护作用程度;(2)评估通过预防性给予类胡萝卜素预防皮肤癌的假设是否基于UVB诱导的DNA损伤的减少。23名健康志愿者口服类胡萝卜素(150毫克/天),持续4周。对血清水平进行定量,范围为390至1710微克/分升。在给予类胡萝卜素前后,通过标准光测试确定UVA和UVB的最小红斑量(MED)以及PUVA的最小光毒量(MPD)。通过放射自显影测量治疗前后UVB照射后非程序性DNA合成(UDS)来评估DNA损伤。通过比较给予类胡萝卜素前后的红斑剂量,未发现类胡萝卜素对UVA、UVB和PUVA红斑有统计学上显著的依赖性保护作用。在DNA水平上也没有迹象表明所采用的方法能检测到保护作用:类胡萝卜素治疗后UVB诱导的UDS量没有减少。我们得出结论:(1)类胡萝卜素不会减少人皮肤中UVB、UVA或PUVA诱导的红斑;(2)活性氧可能不参与PUVA红斑的产生,或者类胡萝卜素在体内可能无法充分淬灭这些自由基;(3)类胡萝卜素对UVB诱导的致癌作用的保护作用不是通过减少DNA中诱变损伤的数量来实现的。

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