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采用液相色谱-高分辨质谱法鉴定三种人肝制剂中硫丹硫酸盐的代谢物并分析其谱图。

Metabolite identification and profile of endosulfan sulfate in three human liver preparations using liquid chromatography-high resolution mass spectrometry.

机构信息

Department of Agricultural Biotechnology and Research Institute of Agriculture and Life Sciences, Seoul National University, Seoul 08826, Republic of Korea.

College of Pharmacy, The Catholic University of Korea, Kyeonggi-do 14662, Republic of Korea.

出版信息

J Chromatogr B Analyt Technol Biomed Life Sci. 2020 Mar 1;1140:121996. doi: 10.1016/j.jchromb.2020.121996. Epub 2020 Jan 28.

Abstract

In this study, we performed the metabolism of endosulfan sulfate in human liver preparations (human liver microsomes, S9 fractions and hepatocytes) to identify new metabolites using liquid chromatography-high resolution mass spectrometry (LC-HRMS). Endosulfan sulfate is a major oxidized metabolite of the organochlorine insecticide endosulfan, and it exhibits a similar toxicity to endosulfan. Six metabolites, including 5 novel metabolites of endosulfan sulfate, were identified in the three different human liver reaction mixtures and metabolic pathways of endosulfan sulfate were proposed. The phase I metabolites M1 and M2 were observed in human liver microsomes, S9 fractions and hepatocytes. M1 was suggested to be an endosulfan diol monosulfate and M2 was identified as (1,4,5,6,7,7-hexachloro-3-formylbicyclo[2,2,1]hept-5-en-2-yl)methyl hydrogen sulfate through the interpretation of the HRMS spectrum. The phase II metabolite M3 was produced as an endosulfan sulfate-GSH conjugate in those three liver preparations and transformed to M5 (dipeptide) in S9 fractions and hepatocytes. M3 was the most predominant metabolite identified in the three liver preparations. M4 was only detected in microsomes as an M2-GSH conjugate and was metabolized to M6 (monopeptide) in hepatocytes. These results are different from the metabolic pathway of endosulfan and suggest the possible detoxification metabolic reaction of endosulfan sulfate in living organisms.

摘要

在这项研究中,我们用人肝制剂(人肝微粒体、S9 级分和肝细胞)进行了硫丹硫酸盐的代谢研究,使用液相色谱-高分辨质谱(LC-HRMS)来鉴定新的代谢物。硫丹硫酸盐是有机氯杀虫剂硫丹的主要氧化代谢物,其毒性与硫丹相似。在这三种不同的人肝反应混合物中,共鉴定出 6 种代谢物,包括 5 种硫丹硫酸盐的新代谢物,并提出了硫丹硫酸盐的代谢途径。人肝微粒体、S9 级分和肝细胞中均观察到 I 相代谢物 M1 和 M2。M1 被认为是硫丹二醇单硫酸盐,M2 通过 HRMS 谱的解析被鉴定为(1,4,5,6,7,7-六氯-3-甲酰基双环[2,2,1]庚-5-烯-2-基)甲基硫酸氢盐。II 相代谢物 M3 在这三种肝制剂中作为硫丹硫酸盐-GSH 缀合物生成,并在 S9 级分和肝细胞中转化为 M5(二肽)。M3 是这三种肝制剂中鉴定出的最主要的代谢物。M4 仅在微粒体中作为 M2-GSH 缀合物被检测到,并在肝细胞中代谢为 M6(单肽)。这些结果与硫丹的代谢途径不同,提示硫丹硫酸盐在生物体中可能存在解毒代谢反应。

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