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cDNA 表达的人细胞色素 P450 对 OPT 农药脱硫的动力学参数。

Kinetic parameters of OPT pesticide desulfuration by c-DNA expressed human CYPs.

机构信息

Comparative Toxicology and Ecotoxicology Laboratory, Istituto Superiore di Sanità, Viale Regina Elena 299, I-00161 Rome, Italy.

出版信息

Environ Toxicol Pharmacol. 2002 Jul;11(3-4):181-90. doi: 10.1016/s1382-6689(02)00010-8.

DOI:10.1016/s1382-6689(02)00010-8
PMID:21782601
Abstract

The role of different cytochrome P450 isoforms (CYPs) in the desulfuration of four organophosphorothionate pesticides (OPTs), namely diazinon (DIA), azinphos-methyl (AZ), chlorpyrifos (CPF) and parathion (PARA), at OPT levels representative of actual human exposure has been investigated. For this purpose c-DNA expressed human CYPs and a method, based on acetylcholinesterase (AChE) inhibition, able to detect nM levels of oxon have been used. Our results indicate that the four tested OPTs at low concentration were mainly desulfurated by CYP2B6, 2C19 and 1A2, showing K(m) values in the range 0.8-5 μM and the highest efficiency (intrinsic clearance (ICL)) values. CYP3A4 was generally endowed with high K(m) and resulted linear up to 25-100 μM OPT, concentrations saturating the most efficient CYPs. The tentative extrapolation of the relative contribution of single CYPs, taking into account the average content of different isoforms in the human liver, indicate that CYP1A2 is the major responsible for oxon formation. Indeed this CYP catalyses the 50-90% of desulfuration reaction, depending on the OPT. As CYP3A4 activity is not completely saturated up to 100 μM OPT, and due to the high hepatic content, its contribution to oxon formation may result relevant in poisoning episodes, when individuals are exposed at high doses of OPTs.

摘要

已经研究了不同细胞色素 P450 同工酶 (CYPs) 在四种有机磷硫代酸盐 (OPTs) 脱硫中的作用,即敌百虫 (DIA)、甲拌磷 (AZ)、毒死蜱 (CPF) 和对硫磷 (PARA),这些 OPT 的水平代表了实际的人类暴露水平。为此,使用了表达人 CYP 的 cDNA 和一种基于乙酰胆碱酯酶 (AChE) 抑制的方法,能够检测到纳摩尔水平的氧肟酸。我们的结果表明,四种测试的 OPT 在低浓度下主要由 CYP2B6、2C19 和 1A2 脱硫,表现出 0.8-5 μM 的 K(m) 值和最高效率 (内在清除率 (ICL)) 值。CYP3A4 通常具有较高的 K(m) 值,在 25-100 μM OPT 范围内呈线性增加,达到最有效 CYP 的浓度饱和。考虑到人肝中不同同工酶的平均含量,对单个 CYP 的相对贡献进行推测性外推,表明 CYP1A2 是形成氧肟酸的主要原因。事实上,这种 CYP 催化 50-90%的脱硫反应,具体取决于 OPT。由于 CYP3A4 的活性在 100 μM OPT 下并未完全饱和,并且由于其在肝脏中的含量较高,因此在个体暴露于高剂量 OPT 时发生中毒事件时,其对氧肟酸形成的贡献可能会变得相关。

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