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1,1-二氯乙烯诱导的克拉拉细胞损伤与反应性环氧化物的原位形成有关。其谷胱甘肽共轭物的免疫组织化学检测。

1,1-Dichloroethylene-induced Clara cell damage is associated with in situ formation of the reactive epoxide. Immunohistochemical detection of its glutathione conjugate.

作者信息

Forkert P G

机构信息

Department of Anatomy and Cell Biology, Queen's University, Kingston, Ontario, Canada.

出版信息

Am J Respir Cell Mol Biol. 1999 Jun;20(6):1310-8. doi: 10.1165/ajrcmb.20.6.3525.

Abstract

Pulmonary Clara cells are selectively damaged in mice given 1, 1-dichloroethylene (DCE), a chemical used in the plastics industry. The cytotoxicity is attributed to formation of a reactive metabolite believed to be the DCE-epoxide, which was detected in vitro. We have undertaken in vivo studies to test the hypothesis that in situ formation of the DCE-epoxide within Clara cells mediates the cell-specific injury manifested after DCE exposure. Formation of the epoxide was estimated by trapping of the metabolite with glutathione (GSH) and identifying the conjugated products as 2-(S-glutathionyl) acetyl glutathione ([B]) and 2-S-glutathionyl acetate ([C]). High-pressure liquid chromatographic analyses showed that conjugates [B] and [C] were both detected in lung cytosol isolated from mice treated in vivo with [14C]DCE. Epoxide levels in the cytosol, as estimated by the total amount of conjugates formed, were dose-dependent at DCE doses ranging from 25 to 225 mg/kg. Pretreatment of mice with buthionine sulfoximine (BSO) decreased sulfhydryl levels and significantly inhibited the formation of the GSH conjugates. Epoxide levels were also reduced by pretreatment with diallyl sulfone (DASO2), an inhibitor of the P450 isozyme CYP2E1. A polyclonal antibody was developed that is specific for conjugate [C] and that recognizes an antigen consisting of the conjugate epoxide-GSH-glutaraldehyde-bovine serum albumin. Immunohistochemical studies with this antibody revealed staining in Clara cells of mice treated with DCE. Staining was also present in Clara cells of mice treated with both BSO and DCE, but at slightly reduced levels. Reduction of this staining was more pronounced in Clara cells of mice treated with both DASO2 and DCE. These results show that the DCE-epoxide is formed in vivo, is localized in Clara cells, and correlates with the cytotoxicity manifested in this cell type.

摘要

在给予1,1 - 二氯乙烯(DCE,一种塑料工业中使用的化学物质)的小鼠中,肺克拉拉细胞会被选择性损伤。细胞毒性归因于一种被认为是DCE - 环氧化物的反应性代谢产物的形成,该产物已在体外被检测到。我们进行了体内研究,以检验以下假设:克拉拉细胞内DCE - 环氧化物的原位形成介导了DCE暴露后出现的细胞特异性损伤。通过用谷胱甘肽(GSH)捕获代谢产物并将共轭产物鉴定为2 -(S - 谷胱甘肽基)乙酰谷胱甘肽([B])和2 - S - 谷胱甘肽基乙酸酯([C])来估计环氧化物的形成。高压液相色谱分析表明,共轭物[B]和[C]在从用[14C]DCE进行体内处理的小鼠分离的肺细胞溶质中均被检测到。根据形成的共轭物总量估计,细胞溶质中的环氧化物水平在25至225 mg/kg的DCE剂量范围内呈剂量依赖性。用丁硫氨酸亚砜胺(BSO)预处理小鼠会降低巯基水平,并显著抑制GSH共轭物的形成。用二烯丙基砜(DASO2,一种细胞色素P450同工酶CYP2E1的抑制剂)预处理也会降低环氧化物水平。开发了一种针对共轭物[C]的特异性多克隆抗体,该抗体识别由共轭环氧化物 - GSH - 戊二醛 - 牛血清白蛋白组成的抗原。用该抗体进行的免疫组织化学研究显示,在用DCE处理的小鼠的克拉拉细胞中有染色。在用BSO和DCE两者处理的小鼠的克拉拉细胞中也存在染色,但水平略有降低。在用DASO2和DCE两者处理的小鼠的克拉拉细胞中,这种染色的减少更为明显。这些结果表明,DCE - 环氧化物在体内形成,定位于克拉拉细胞中,并且与该细胞类型中表现出的细胞毒性相关。

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