Aluru Neelakanteswar, Renaud Rick, Leatherland John F, Vijayan Mathilakath M
Department of Biology, University of Waterloo, Ontario, Canada N2L 3G1.
Toxicol Sci. 2005 Apr;84(2):260-9. doi: 10.1093/toxsci/kfi077. Epub 2005 Jan 5.
The objective of the study was to investigate the impact of aryl hydrocarbon receptor (AhR) activation on interrenal steroidogenesis in rainbow trout. To this end, fish were fed AhR agonist (beta-naphthoflavone (BNF): 10 mg/kg body mass/day) and antagonist (alpha-naphthoflavone (ANF): 10 mg/kg body mass/day) either singly or in combination (ABNF) for 5 days to elucidate the mechanisms involved in AhR-mediated depression of cortisol production. Liver AhR protein expression was significantly elevated only with ABNF, but not with BNF and ANF compared to the control group. However, all three treatments (BNF, ANF, and ABNF) significantly elevated cytochrome P450 1A1 (CYP1A1) gene and protein expression in the kidney and liver, respectively. Also, these three treatment groups had significantly depressed ACTH-stimulated cortisol production in vitro compared to the control group. This attenuation of interrenal steroidogenesis corresponded with a lower mRNA abundance of steroidogenic acute regulatory (StAR) protein and cytochrome P450 cholesterol side chain cleavage enzyme (P450scc), but not 11beta-hydroxylase. Furthermore, in vitro incubation of head kidney pieces with 7-3H-pregnenolone failed to show any treatment effects on pathways downstream of P450scc, except for a significantly higher conversion to progesterone in the BNF and ANF groups. Plasma cortisol and glucose levels showed no significant change between the treated groups and control, but liver and brain glucocorticoid receptor (GR) protein expression was higher in the BNF group, and ANF abolished this response. Taken together, both BNF and ANF impaired cortisol production, and the mechanism may involve attenuation of StAR and P450scc, the rate limiting steps in steroidogenesis. Overall, endocrine disruption by xenobiotics acting via AhR includes impaired cortisol biosynthesis and abnormal cortisol target tissue GR responses in rainbow trout.
本研究的目的是调查芳烃受体(AhR)激活对虹鳟鱼肾间组织类固醇生成的影响。为此,将鱼单独或联合投喂AhR激动剂(β-萘黄酮(BNF):10毫克/千克体重/天)和拮抗剂(α-萘黄酮(ANF):10毫克/千克体重/天)(ABNF),持续5天,以阐明AhR介导的皮质醇生成抑制所涉及的机制。与对照组相比,仅ABNF显著提高了肝脏AhR蛋白表达,而BNF和ANF则未使其升高。然而,所有三种处理(BNF、ANF和ABNF)分别显著提高了肾脏和肝脏中细胞色素P450 1A1(CYP1A1)基因和蛋白表达。此外,与对照组相比,这三个处理组在体外显著抑制了促肾上腺皮质激素刺激的皮质醇生成。肾间组织类固醇生成的这种减弱与类固醇生成急性调节蛋白(StAR)和细胞色素P450胆固醇侧链裂解酶(P450scc)的mRNA丰度降低相对应,但与11β-羟化酶无关。此外,用7-³H-孕烯醇酮对头肾组织块进行体外孵育,除了BNF和ANF组转化为孕酮的比例显著更高外,未显示出对P450scc下游途径的任何处理效果。处理组与对照组之间血浆皮质醇和葡萄糖水平无显著变化,但BNF组肝脏和脑糖皮质激素受体(GR)蛋白表达较高,而ANF消除了这种反应。综上所述,BNF和ANF均损害了皮质醇生成,其机制可能涉及StAR和P450scc的减弱,这是类固醇生成中的限速步骤。总体而言,通过AhR起作用的外源性物质引起的内分泌干扰包括虹鳟鱼皮质醇生物合成受损和皮质醇靶组织GR反应异常。