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壬基酚处理的FVB/NJ小鼠中细胞色素P450的性别特异性诱导

Gender-specific induction of cytochrome P450s in nonylphenol-treated FVB/NJ mice.

作者信息

Hernandez Juan P, Chapman Laura M, Kretschmer Xiomara C, Baldwin William S

机构信息

Biological Sciences, University of Texas at El Paso, 500 W. University Ave., El Paso, TX 79968, USA.

出版信息

Toxicol Appl Pharmacol. 2006 Oct 15;216(2):186-96. doi: 10.1016/j.taap.2006.05.014. Epub 2006 May 25.

Abstract

Nonylphenol (NP) is a breakdown product of nonylphenol ethoxylates, which are used in a variety of industrial, agricultural, household cleaning, and beauty products. NP is one of the most commonly found toxicants in the United States and Europe and is considered a toxicant of concern because of its long half-life. NP is an environmental estrogen that also activates the pregnane X-receptor (PXR) and in turn induces P450s. No study to date has examined the gender-specific effects of NP on hepatic P450 expression. We provided NP at 0, 50 or 75 mg/kg/day for 7 days to male and female FVB/NJ mice and compared their P450 expression profiles. Q-PCR was performed on hepatic cDNA using primers to several CYP isoforms regulated by PXR or its relative, the constitutive androstane receptor (CAR). In female mice, NP induced Cyp2b10 and Cyp2b13, and downregulated the female-specific P450s, Cyp3a41 and Cyp3a44. In contrast, male mice treated with NP showed increased expression of Cyp2a4, Cyp2b9, and Cyp2b10. Western blots confirmed induction of Cyp2b subfamily members in both males and females. Consistent with the Q-PCR data, Western blots showed dose-dependent downregulation of Cyp3a only in females and induction of Cyp2a only in males. The overall increase in female-predominant P450s in males (Cyp2a4, 2b9) and the decrease in female-predominant P450s in females (Cyp3a41, 3a44) suggest that NP is in part feminizing the P450 profile in males and masculinizing the P450 profile in females. Testosterone hydroxylation was also altered in a gender-specific manner, as testosterone 16alpha-hydroxylase activity was only induced in NP-treated males. In contrast, NP-treated females demonstrated a greater propensity for metabolizing zoxazolamine probably due to greater Cyp2b induction in females. In conclusion, NP causes gender-specific P450 induction and therefore exposure to NP may cause distinct pharmacological and toxicological effects in males compared to females.

摘要

壬基酚(NP)是壬基酚聚氧乙烯醚的分解产物,壬基酚聚氧乙烯醚用于各种工业、农业、家用清洁和美容产品中。NP是美国和欧洲最常见的有毒物质之一,因其半衰期长而被视为一种值得关注的有毒物质。NP是一种环境雌激素,它还能激活孕烷X受体(PXR),进而诱导细胞色素P450(P450s)。迄今为止,尚无研究考察NP对肝脏P450表达的性别特异性影响。我们以0、50或75mg/kg/天的剂量给雄性和雌性FVB/NJ小鼠提供NP,持续7天,并比较它们的P450表达谱。使用针对几种受PXR或其相关物组成型雄甾烷受体(CAR)调控的CYP同工型的引物,对肝脏cDNA进行定量聚合酶链反应(Q-PCR)。在雌性小鼠中,NP诱导Cyp2b10和Cyp2b13,并下调雌性特异性P450s,即Cyp3a41和Cyp3a44。相比之下,用NP处理的雄性小鼠Cyp2a4、Cyp2b9和Cyp2b10的表达增加。蛋白质免疫印迹法证实了雄性和雌性中Cyp2b亚家族成员的诱导。与Q-PCR数据一致,蛋白质免疫印迹法显示仅在雌性中Cyp3a呈剂量依赖性下调,仅在雄性中Cyp2a被诱导。雄性中以雌性为主的P450s(Cyp2a4、2b9)总体增加,而雌性中以雌性为主的P450s(Cyp3a41、3a44)减少,这表明NP在一定程度上使雄性的P450谱女性化,使雌性的P450谱男性化。睾酮羟基化也以性别特异性方式改变,因为仅在NP处理的雄性中诱导了睾酮16α-羟基化酶活性。相比之下,NP处理的雌性表现出更高的唑沙仑代谢倾向,这可能是由于雌性中Cyp2b诱导程度更高。总之,NP导致性别特异性的P450诱导,因此与雌性相比,接触NP可能在雄性中引起不同的药理和毒理效应。

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