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二羟基丙酮是免晒美黑乳液中的活性褐变成分,可诱导培养的HaCaT角质形成细胞发生DNA损伤、细胞周期阻滞和凋亡。

Dihydroxyacetone, the active browning ingredient in sunless tanning lotions, induces DNA damage, cell-cycle block and apoptosis in cultured HaCaT keratinocytes.

作者信息

Petersen Anita B, Wulf Hans Christian, Gniadecki Robert, Gajkowska Barbara

机构信息

Department of Dermatology, Bispebjerg Hospital, Bispebjerg Bakke 23, DK-2400 Copenhagen, NV, Denmark.

出版信息

Mutat Res. 2004 Jun 13;560(2):173-86. doi: 10.1016/j.mrgentox.2004.03.002.

Abstract

Dihydroxyacetone (DHA), the active substance in sunless tanning lotions reacts with the amino groups of proteins to form a brown-colored complex. This non-enzymatic glycation, known as the Maillard reaction, can also occur with free amino groups in DNA, raising the possibility that DHA may be genotoxic. To address this issue we investigated the effects of DHA on cell survival and proliferation of a human keratinocyte cell line, HaCaT. Dose- and time-dependent morphological changes, chromatin condensation, cytoplasmic budding and cell detachment were seen in cells treated with DHA. Several dead cells were observed after long-time (24 h) incubation with 25 mM DHA or more. Furthermore, an extensive decline in proliferation was observed 1 day after DHA exposure for 24 h. When applied in different concentrations (5-50 mM) and for different time periods (1, 3 or 24 h) DHA caused a G(2)/M block after the cyclin B(1) restriction point. Exit from this cell-cycle block was associated with massive apoptosis, as revealed by a clonogenic assay, TUNEL staining and electron microscopy. Furthermore, DHA caused DNA damage as revealed by the alkaline comet assay. Preincubation with antioxidants prevented the formation of DNA strand breaks. The DHA toxicity may be caused by direct redox reactions, with formation of ROS as the crucial intermediates. The genotoxic capacity of DHA raises a question about the long-term clinical consequences of treatment of the skin with this commonly used compound.

摘要

二羟基丙酮(DHA)是免晒美黑乳液中的活性物质,它与蛋白质的氨基反应形成棕色复合物。这种非酶糖基化反应,即美拉德反应,也可能发生在DNA中的游离氨基上,这增加了DHA可能具有基因毒性的可能性。为了解决这个问题,我们研究了DHA对人角质形成细胞系HaCaT细胞存活和增殖的影响。在用DHA处理的细胞中观察到了剂量和时间依赖性的形态变化、染色质浓缩、细胞质出芽和细胞 detachment。在用25 mM或更高浓度的DHA长时间(24小时)孵育后,观察到了几个死细胞。此外,在DHA暴露24小时后1天,观察到增殖大幅下降。当以不同浓度(5-50 mM)和不同时间段(1、3或24小时)应用时,DHA在细胞周期蛋白B1限制点后导致G2/M期阻滞。如克隆形成试验、TUNEL染色和电子显微镜所示,从这种细胞周期阻滞中退出与大量细胞凋亡有关。此外,碱性彗星试验显示DHA会导致DNA损伤。用抗氧化剂预孵育可防止DNA链断裂的形成。DHA的毒性可能是由直接氧化还原反应引起的,其中ROS的形成是关键中间体。DHA的基因毒性能力引发了关于用这种常用化合物治疗皮肤的长期临床后果的问题。

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