Pilipenko Nadezhda, Ropstad Erik, Halsne Ruth, Zamaratskaia Galia
Department of Molecular Sciences, Swedish University of Agricultural Sciences, P.O. Box 7015, 750 07 Uppsala, Sweden.
Department of Production Animal Clinical Sciences, Faculty of Veterinary Medicine and Biosciences, Norwegian University of Life Sciences, P.O. 8146 Dep., 0033 Oslo, Norway.
Biomed Res Int. 2017;2017:8472312. doi: 10.1155/2017/8472312. Epub 2017 May 8.
The aim of the present study was to evaluate in vitro effects of dietary phytochemicals naringenin, quercetin, and sesamin on the activities of ethoxy- (EROD; CYP1A) and benzyloxy- (BROD; CYP3A) resorufin O-dealkylases after the exposure to the cocktail of persistent organic pollutants (POPs). CD-1 mice were exposed from weaning, through gestation and lactation to a defined mixture of POPs. Hepatic microsomes were prepared from their female offspring at postnatal day 42. Hepatic EROD and BROD activity were evaluated in the presence of quercetin, naringenin, and sesamin at nine concentrations from 5 to 100000 nM. EROD activity was strongly inhibited by quercetin with values from 1.7 to 2.6 M. BROD activity was inhibited by quercetin with values from 64.9 to 75.3 M and naringenin with values from 39.3 to 45.8 M. The IC and values did not differ between the groups of mice with different levels of POPs exposure in any of the experimental sets. Sesamin did not inhibit either EROD or BROD. We concluded that the interactions of quercetin and naringenin with CYP1A and CYP3A in mice liver were not affected by the levels of POPs exposure.
本研究的目的是评估膳食植物化学物质柚皮素、槲皮素和芝麻素在暴露于持久性有机污染物(POPs)混合物后对乙氧基(EROD;CYP1A)和苄氧基(BROD;CYP3A)试卤灵O - 脱烷基酶活性的体外影响。CD - 1小鼠从断奶期开始,经妊娠和哺乳期暴露于特定的POPs混合物中。在出生后第42天从它们的雌性后代中制备肝微粒体。在存在浓度从5到100000 nM的槲皮素、柚皮素和芝麻素的情况下评估肝EROD和BROD活性。槲皮素对EROD活性有强烈抑制作用,IC50值为1.7至2.6 μM。槲皮素对BROD活性有抑制作用,IC50值为64.9至75.3 μM,柚皮素对BROD活性的IC50值为39.3至45.8 μM。在任何实验组中,不同POPs暴露水平的小鼠组之间的IC50和EC50值没有差异。芝麻素对EROD或BROD均无抑制作用。我们得出结论,槲皮素和柚皮素与小鼠肝脏中CYP1A和CYP3A的相互作用不受POPs暴露水平的影响。