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本文引用的文献

1
Sulfate metabolites of 4-monochlorobiphenyl in whole poplar plants.杨树植株中 4-单氯联苯的硫酸盐代谢物。
Environ Sci Technol. 2013 Jan 2;47(1):557-62. doi: 10.1021/es303807f. Epub 2012 Dec 14.
2
Identification of sulfated metabolites of 4-chlorobiphenyl (PCB3) in the serum and urine of male rats.鉴定雄性大鼠血清和尿液中 4-氯联苯(PCB3)的硫酸代谢物。
Chem Res Toxicol. 2012 Dec 17;25(12):2796-804. doi: 10.1021/tx300416v. Epub 2012 Nov 16.
3
New hydroxylated metabolites of 4-monochlorobiphenyl in whole poplar plants.全杨树植株中4-单氯联苯的新羟基化代谢产物。
Chem Cent J. 2011 Dec 20;5:87. doi: 10.1186/1752-153X-5-87.
4
1-Aminobenzotriazole, a known cytochrome P450 inhibitor, is a substrate and inhibitor of N-acetyltransferase.1-氨基苯并三唑是一种已知的细胞色素 P450 抑制剂,也是 N-乙酰基转移酶的底物和抑制剂。
Drug Metab Dispos. 2011 Sep;39(9):1674-9. doi: 10.1124/dmd.111.039834. Epub 2011 Jun 15.
5
Identification of hydroxylated metabolites of 3,3',4,4'-tetrachlorobiphenyl and metabolic pathway in whole poplar plants.鉴定 3,3',4,4'-四氯联苯的羟基化代谢物及在整株杨树上的代谢途径。
Chemosphere. 2010 Sep;81(4):523-8. doi: 10.1016/j.chemosphere.2010.07.036. Epub 2010 Aug 12.
6
Hydroxylated metabolites of 4-monochlorobiphenyl and its metabolic pathway in whole poplar plants.4-单氯联苯的羟基化代谢产物及其在整株杨树上的代谢途径。
Environ Sci Technol. 2010 May 15;44(10):3901-7. doi: 10.1021/es100230m.
7
Hydroxylated polychlorinated biphenyls (OH-PCBs) in the blood of mammals and birds from Japan: lower chlorinated OH-PCBs and profiles.日本哺乳动物和鸟类血液中的羟基化多氯联苯(OH-PCBs):低氯代OH-PCBs及其分布特征
Chemosphere. 2009 Feb;74(7):950-61. doi: 10.1016/j.chemosphere.2008.10.038. Epub 2008 Dec 2.
8
Is 1-aminobenzotriazole an appropriate in vitro tool as a nonspecific cytochrome P450 inactivator?1-氨基苯并三唑作为一种非特异性细胞色素P450灭活剂,是否是一种合适的体外工具?
Drug Metab Dispos. 2009 Jan;37(1):10-3. doi: 10.1124/dmd.108.024075. Epub 2008 Oct 20.
9
Mechanistic investigation of the noncytochrome P450-mediated metabolism of triadimefon to triadimenol in hepatic microsomes.肝微粒体中三唑酮经非细胞色素P450介导代谢为三唑醇的机制研究。
Chem Res Toxicol. 2008 Oct;21(10):1997-2004. doi: 10.1021/tx800211t. Epub 2008 Sep 3.
10
Cytochrome p450 and chemical toxicology.细胞色素P450与化学毒理学
Chem Res Toxicol. 2008 Jan;21(1):70-83. doi: 10.1021/tx700079z. Epub 2007 Dec 6.

在整株杨树上对细胞色素 P450 的抑制作用和 4-单氯联苯的羟化作用。

Inhibition of cytochromes P450 and the hydroxylation of 4-monochlorobiphenyl in whole poplar.

机构信息

Department of Civil and Environmental Engineering and IIHR Hydroscience and Engineering, The University of Iowa, Iowa City, Iowa 52242, United States.

出版信息

Environ Sci Technol. 2013 Jul 2;47(13):6829-35. doi: 10.1021/es304298m. Epub 2013 Jan 24.

DOI:10.1021/es304298m
PMID:23320482
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3652898/
Abstract

Cytochromes P450 (CYPs) are potential enzymes responsible for hydroxylation of many xenobiotics and endogenous chemicals in living organisms. It has been found that 4-monochlorobiphenyl (PCB3), mainly an airborne pollutant, can be metabolized to hydroxylated transformation products (OH-PCB3s) in whole poplars. However, the enzymes involved in the hydroxylation of PCB3 in whole poplars have not been identified. Therefore, two CYP suicide inhibitors, 1-aminobenzotriazole (ABT) and 17-octadecynoic acid (ODYA), were selected to probe the hydroxylation reaction of PCB3 in whole poplars in this work. Poplars (Populus deltoides × nigra, DN34) were exposed to PCB3 with or without inhibitor for 11 days. Results showed both ABT and ODYA can decrease the concentrations and yields of five OH-PCB3s in different poplar parts via the inhibition of CYPs. Furthermore, both ABT and ODYA demonstrated a dose-dependent relationship to the formation of OH-PCB3s in whole poplars. The higher the inhibitor concentrations, the lower the total yields of OH-PCB3s. For ABT spiked-additions, the total mass yield of five OH-PCB3s was inhibited by a factor of 1.6 times at an ABT concentration of 2.5 mg L(-1), 4.0 times at 12.5 mg L(-1), and 7.0 times at 25 mg L(-1). For the inhibitor ODYA, the total mass of five OH-PCB3s was reduced by 2.1 times compared to the control at an ODYA concentration of 2.5 mg L(-1). All results pointed to the conclusion that CYP enzymes were the agents which metabolized PCB3 to OH-PCB3s in whole poplars because suicide CYP inhibitors ABT and ODYA both led to sharp decreases of OH-PCB3s formation in whole poplars. A dose-response curve for each of the suicide inhibitors was developed.

摘要

细胞色素 P450(CYPs)是负责许多外来生物和生物体内源性化学物质羟化的潜在酶。已经发现,4-单氯联苯(PCB3),主要是一种空气污染物,可以在整个杨树中代谢为羟化转化产物(OH-PCB3s)。然而,在整个杨树上参与 PCB3 羟化的酶尚未确定。因此,本研究选择了两种 CYP 自杀抑制剂 1-氨基苯并三唑(ABT)和 17-辛炔酸(ODYA)来探测整个杨树上 PCB3 的羟化反应。杨树(杂种黑杨×欧美杨,DN34)用或不用抑制剂暴露于 PCB3 中 11 天。结果表明,ABT 和 ODYA 均可通过抑制 CYP 降低不同杨树部位五种 OH-PCB3s 的浓度和产率。此外,ABT 和 ODYA 均表现出对整个杨树中 OH-PCB3s 形成的剂量依赖性关系。抑制剂浓度越高,OH-PCB3s 的总产量越低。对于 ABT 加标添加,在 ABT 浓度为 2.5 mg L(-1)时,五种 OH-PCB3s 的总质量产率抑制了 1.6 倍,在 12.5 mg L(-1)时抑制了 4.0 倍,在 25 mg L(-1)时抑制了 7.0 倍。对于抑制剂 ODYA,与对照相比,五种 OH-PCB3s 的总质量减少了 2.1 倍。所有结果都表明 CYP 酶是将 PCB3 代谢为 OH-PCB3s 的代谢物,因为自杀 CYP 抑制剂 ABT 和 ODYA 都会导致整个杨树上 OH-PCB3s 形成急剧减少。为每种自杀抑制剂开发了剂量-反应曲线。