Hormonal activity of polycyclic musks evaluated by reporter gene assay.

Taiki Mori, Mitsuru Iida, Hiroshi Ishibashi, Shinya Kohra, Yuji Takao, Takehiro Takemasa, Koji Arizono
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Abstract

Synthetic musk fragrance compounds, such as polycyclic musks (PCMs), are a group of chemicals used extensively as personal care products, and can be found in the environment and the human body. PCMs, such as 1,3,4,6,7,8-hexahydro-4,6,6,7,8,8-hexa-methylcyclopenta-gamma-2-benzopyran (HHCB) and 7-acetyl-1,1,3,4,4,6-hexamethyltetralin (AHTN), are known to have agonistic activities toward human estrogen receptor alpha (hERalpha) and hERbeta, and have antagonistic activity toward the human androgen receptor (hAR), as shown in several reporter gene assays. However, little is known about the interaction of PCMs with the human thyroid hormone receptor (hTR), and the hormonal effects of other PCMs except for HHCB and AHTN. In this study, we focus on the interactions of six PCMs, namely, HHCB, AHTN, 4-acetyl-1,1-dimethyl-6-tert-butyl-indan (ADBI), 6-acetyl-1,1,2,3,3,5-hexamethylindan (AHMI), 6,7-dihydro-1,1,2,3,3-pentamethyl-4(5H)-indanone (DPMI), and 5-acetyl-1,1,2,6-tetramethyl-3-isopropy-lindan (ATII) with hERalpha, hAR, and hTRbeta by in vitro reporter gene assay using Chinese hamster ovary cells. All the samples were found to be agonists toward hERalpha, whereas no agonistic activities of these PCMs for hAR and hTRbeta were observed. No antagonistic activities for hERalpha and hTRbeta were observed at the concentrations tested. However, several PCMs, namely, HHCB, AHTN, ATII, ADBI, and AHMI, showed dose-dependent antagonistic activities for hAR, and the IC50 values of these compounds were estimated to be 1.0 x 10(-7), 1.5 x 10(-7), 1.4 x 10(-7), 9.8 x 10(-6), and 1.4 x 10(-7) M, respectively. The results suggest that these PCMs interact with hERalpha and hAR but have no hormonal effect on hTRbeta. This is the first report on the agonistic and antagonistic activities of ATII, ADBI, AHMI, and DPMI for hERalpha and hAR as determined by in vitro reporter gene assay using stably transfected Chinese hamster ovary cells.

用报告基因法评价多环麝香的激素活性。
合成麝香化合物,如多环麝香(PCMs),是一组广泛用于个人护理产品的化学物质,可以在环境和人体中找到。PCMs,如1,3,4,6,7,8,8 -六氢-4,6,6,7,8,8-六甲基环五- - γ -2-苯并吡喃(HHCB)和7-乙酰-1,1,3,4,4,6-六甲基四乙胺(AHTN),已知对人类雌激素受体α (herα)和herβ具有激动活性,并对人类雄激素受体(hAR)具有拮抗活性,一些报告基因检测显示。然而,关于PCMs与人甲状腺激素受体(hTR)的相互作用,以及除HHCB和AHTN外其他PCMs的激素作用知之甚少。本研究利用中国仓鼠卵巢细胞,通过体外报告基因检测,研究了HHCB、AHTN、4-乙酰基-1,1-二甲基-6-叔丁基-indan (ADBI)、6-乙酰基-1,1,2,3,3,5-六甲基林丹(AHMI)、6,7-二氢-1,1,2,3,3-五甲基-4(5H)-indanone (DPMI)和5-乙酰基-1,1,2,6-四甲基-3-异丙基林丹(ATII) 6种PCMs与herα、hAR和htβ的相互作用。所有样品都被发现是herα的激动剂,而这些PCMs对hAR和htr β没有激动活性。在测试浓度下,未观察到对herα和htr β的拮抗活性。然而,几种PCMs,即HHCB、AHTN、ATII、ADBI和AHMI,对hAR表现出剂量依赖性的拮抗活性,这些化合物的IC50值估计分别为1.0 × 10(-7)、1.5 × 10(-7)、1.4 × 10(-7)、9.8 × 10(-6)和1.4 × 10(-7) M。结果表明,这些PCMs与herα和hAR相互作用,但对herβ没有激素作用。这是第一次用稳定转染的中国仓鼠卵巢细胞进行体外报告基因测定,研究了ATII、ADBI、AHMI和DPMI对hERalpha和hAR的激动和拮抗活性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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