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Reprint of: CYP1A protein expression and catalytic activity in double-crested cormorants experimentally exposed to deepwater Horizon Mississippi Canyon 252 oil

机译:转载:CYp1a蛋白在双冠鸬鹚中的表达和催化活性实验暴露于深水地平线密西西比峡谷252油

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摘要

Double-crested cormorants (Phalacrocorax auritus, DCCO) were orally exposed to Deepwater Horizon Mississippi Canyon 252 (DWH) oil to investigate oil-induced toxicological impacts. Livers were collected for multiple analyses including cytochrome P4501A (CYP1A) enzymatic activity and protein expression. CYP1A enzymatic activity was measured by alkoxyresorufin O-dealkylase (AROD) assays. Activities specific to the O-dealkylation of four resorufin ethers are reported: benzyloxyresorufin O-debenzylase (BROD), ethoxyresorufin O-deethylase (EROD), methoxyresorufin O-demethylase (MROD), and pentoxyresorufin O-depentylase (PROD). CYP1A protein expression was measured by western blot analysis with a CYP1A1 mouse monoclonal antibody. In study 1, hepatic BROD, EROD, and PROD activities were significantly induced in DCCO orally exposed to 20 ml/ kg body weight (bw) oil as a single dose or daily for 5 days. Western blot analysis revealed hepatic CYP1A protein induction in both treatment groups. In study 2 (5 ml/kg bw oil or 10 ml/kg bw oil, 21 day exposure), all four hepatic ARODs were significantly induced. Western blots showed an increase in hepatic CYP1A expression in both treatment groups with a significant induction in birds exposed to 10 ml/kg oil. Significant correlations were detected among all 4 AROD activities in both studies and between CYP1A protein expression and both MROD and PROD activities in study 2. EROD activity was highest for both treatment groups in both studies while BROD activity had the greatest fold-induction. While PROD activity values were consistently low, the fold induction was high, usually 2nd highest to BROD activity. The observed induced AROD profiles detected in the present studies suggest both CYP1A4/1A5 DCCO isoforms are being induced after MC252 oil ingestion. A review of the literature on avian CYP1A AROD activity levels and protein expression after exposure to CYP1A inducers highlights the need for species-specific studies to accurately evaluate avian exposure to oil.
机译:将双冠mor(蝴蝶ala,DCCO)经口暴露于深水地平线密西西比峡谷252(DWH)油中,以研究油引起的毒理学影响。收集肝脏进行多种分析,包括细胞色素P4501A(CYP1A)酶活性和蛋白质表达。 CYP1A酶活性通​​过烷氧基间苯二酚O-脱烷基酶(AROD)分析进行测定。据报道,特定的四种间苯二酚醚的O-脱烷基化活性为:苄氧基间苯二酚O-脱苄基酶(BROD),乙氧基间苯二酚O-脱乙基酶(EROD),甲氧基间苯二酚O-脱甲基酶(MROD)和戊氧基间苯二酚O-脱戊基酶(PROD)。使用CYP1A1小鼠单克隆抗体通过蛋白质印迹分析测量CYP1A蛋白的表达。在研究1中,以口服DCCO的单次剂量或每天5天,可显着诱导肝BROD,EROD和PROD活性。 Western印迹分析显示两个治疗组中的肝CYP1A蛋白诱导。在研究2中(5 ml / kg体重的油或10 ml / kg体重的油,暴露21天),所有四个肝脏AROD均被显着诱导。 Western印迹显示两个治疗组中肝CYP1A表达均增加,暴露于10 ml / kg油中的家禽显着诱导。在两项研究中,在所有4种AROD活性之间以及在CYP1A蛋白表达与MROD和PROD活性之间均检测到显着相关性。在两项研究中,两个治疗组的EROD活性最高,而BROD活性具有最大的诱导倍数。尽管PROD活性值始终较低,但折叠诱导较高,通常是BROD活性的第二高。在本研究中观察到的诱导的AROD概况表明,MC252的油摄入后,CYP1A4 / 1A5 DCCO亚型都被诱导。 CYP1A诱导剂暴露后对禽类CYP1A AROD活性水平和蛋白质表达的文献综述强调了需要进行特定物种研究以准确评估禽类对油的暴露。

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