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首页> 外文期刊>The Journal of toxicological sciences >Cytochrome P450-inhibitory activity of parabens and phthalates used in consumer products
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Cytochrome P450-inhibitory activity of parabens and phthalates used in consumer products

机译:消费类产品中对羟基苯甲酸酯和邻苯二甲酸酯的细胞色素P450抑制活性

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The in vitro cytochrome P450 (CYP)-inhibitory effects of 11 parabens and 7 phthalates used in consumer products, as well as their hydrolytic metabolites, were investigated, using rat liver microsomes as an enzyme source. The effects on individual CYP isozymes were evaluated by assaying inhibition of activities towards specific substrates, i.e., ethoxyresorufin O-dealkylase (EROD), methoxyresorufin O-dealkylase (MROD), pentoxyresorufin O-dealkylase (PROD), 7-benzyloxy-4-trifluoromethylcoumarin dealkylase (BFCD), 7-methoxy-4-trifiuoromethylcoumarin dealkylase (MFCD) and 7-ethoxy-4-trifluoromethylcoumarin dealkylase (EFCD) activities. These activities were dose-dependently inhibited, most potently by medium-side-chain parabens (C6-9) and phthalates (C4-6), and less potently by shorter and longer-side-chain esters. The hydrolytic product of parabens, 4-hydroxybenzoic acid, was not inhibitory, while those of phthalates, phthalic acid monoesters, showed lower inhibitory activity than the parent phthalates. Parabens showed relatively potent inhibition of MFCD activity, considered to be mainly due to CYP2C, and phthalates showed relatively potent inhibition of PROD activity, considered to be mainly due to CYP2B.
机译:使用大鼠肝微粒体作为酶源,研究了消费品中使用的11种对羟基苯甲酸酯和7种邻苯二甲酸酯及其水解代谢产物的体外细胞色素P450(CYP)抑制作用。通过测定对特定底物的活性的抑制作用来评估对单个CYP同工酶的影响,这些底物是乙氧基间苯二酚O-脱烷基酶(EROD),甲氧基间苯二酚O-脱烷基酶(MROD),戊氧基间苯二酚O-脱烷基酶(PROD),7-苄氧基-4-三氟甲基香豆素脱烷基酶(BFCD),7-甲氧基-4-三氟甲基香豆素脱烷基酶(MFCD)和7-乙氧基-4-三氟甲基香豆素脱烷基酶(EFCD)的活性。这些活性受到剂量依赖性的抑制,最受中侧对羟基苯甲酸酯(C6-9)和邻苯二甲酸酯(C4-6)抑制,而对较短和较长侧链酯的抑制作用较小。对羟基苯甲酸酯的水解产物4-羟基苯甲酸没有抑制作用,而邻苯二甲酸酯的邻苯二甲酸单酯的水解产物显示出比母体邻苯二甲酸酯更低的抑制活性。对羟基苯甲酸酯类显示出对MFCD活性的相对有效的抑制作用,这主要归因于CYP2C,而邻苯二甲酸酯类则表现出对PROD活性的相对有效的抑制作用,认为主要归因于CYP2B。

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