College of Pharmacy, Seoul National University, Seoul 08826, Republic of Korea; Natural Products Research Institute, Seoul National University, Seoul 08826, Republic of Korea.
College of Pharmacy, Seoul National University, Seoul 08826, Republic of Korea; Natural Products Research Institute, Seoul National University, Seoul 08826, Republic of Korea; Toxicology Division, IEC Korea, Suwon 17074, Republic of Korea.
Toxicol In Vitro. 2020 Sep;67:104886. doi: 10.1016/j.tiv.2020.104886. Epub 2020 May 11.
Benzophenone-3 (BP-3) and benzopenone-8 (BP-8) are commonly used ultraviolet (UV) filter ingredients in diverse sunscreen products. Recently, the obesogenic activity of avobenzone, a long wave UV A filter, was elucidated in the adipogenesis model of human bone marrow mesenchymal stem cells (hBM-MSCs). In this study, the obesogenic potentials of BP-3 and BP-8 were investigated because of their chemical similarity to avobenzone. During the adipogenesis in hBM-MSCs, BP-3 and BP-8 (EC, 25.05 and 43.20 μM, respectively) potently promoted adiponectin secretion than avobenzone (EC, 72.69 μM). In target identification, both BP-3 and BP-8 directly bound to peroxisome proliferator-activated receptor γ (PPARγ), which was associated with the recruitment of steroid receptor coactivator-2 (SRC-2). BP-3 functioned as a PPARγ full agonist whereas BP-8 was a PPARγ partial agonist. In addition, BP-3 and BP-8 significantly increased the gene transcription of PPARα, PPARγ, and major lipid metabolism-associated enzymes in human epidermal keratinocytes, a major target site of UV filters in human skin. This study suggests that BP-3 and BP-8 are obesogenic environmental chemicals similar to phthalates, bisphenols, and organotins.
二苯甲酮-3(BP-3)和二苯甲酮-8(BP-8)是各种防晒霜中常用的紫外线(UV)过滤成分。最近,长波紫外线 A 过滤器阿伏苯宗在人骨髓间充质干细胞(hBM-MSCs)成脂分化模型中的致肥胖活性得到了阐明。由于与阿伏苯宗具有化学相似性,本研究研究了 BP-3 和 BP-8 的致肥胖潜力。在 hBM-MSCs 的成脂分化过程中,BP-3 和 BP-8(EC50 值分别为 25.05 和 43.20 μM)比阿伏苯宗(EC50 值为 72.69 μM)更有效地促进脂联素分泌。在靶标鉴定中,BP-3 和 BP-8 均可直接与过氧化物酶体增殖物激活受体γ(PPARγ)结合,这与类固醇受体共激活因子-2(SRC-2)的募集有关。BP-3 是 PPARγ 完全激动剂,而 BP-8 是 PPARγ 部分激动剂。此外,BP-3 和 BP-8 可显著增加人表皮角质形成细胞中 PPARα、PPARγ 和主要脂质代谢相关酶的基因转录,人表皮角质形成细胞是人皮肤中紫外线滤光剂的主要靶位。本研究表明,BP-3 和 BP-8 是与邻苯二甲酸酯、双酚和有机锡类似的致肥胖环境化学物质。