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低剂量莠去津暴露饮用水诱导小鼠肝损伤模型的建立及验证

朱玉 苏莹实 刘溪 何宝国 秦嫘

中国比较医学杂志2024,Vol.34Issue(6):73-81,9.
中国比较医学杂志2024,Vol.34Issue(6):73-81,9.DOI:10.3969/j.issn.1671-7856.2024.06.009

低剂量莠去津暴露饮用水诱导小鼠肝损伤模型的建立及验证

Establishment and validation of a mouse liver injury model induced by chronic low-dose exposure to atrazine

朱玉 1苏莹实 1刘溪 1何宝国 1秦嫘1

作者信息

  • 1. 齐齐哈尔医学院,黑龙江齐齐哈尔 161006
  • 折叠

摘要

Abstract

Objective To establish a model of long-term atrazine(ATR)-induced liver injury in mice and to evaluate the hepatotoxic effects induced by ATR.Methods C57BL/6-N male mice were randomly divided into a control group and 1.5 mg/L and 150 mg/L ATR dose(ATR-L,ATR-H)groups.After 35 and 63 days,serum liver function biochemical indexes and inflammatory factors were detected,the hepatosomatic ratio was calculated,and the histopathology and ultrastructure of the liver were observed.Lipid peroxidation levels and antioxidant capacity,the activities of major phase I metabolic enzymes and phase Ⅱ detoxification enzymes,and the expression of related proteins in liver tissues were detected.Results Compared with the control group,the ATR groups showed significant changes in the AST/ALT ratio,levels of pro-inflammatory factors CCL2,TNF-α and IL-6,H2O2 content and activities of the metabolic enzymes NCR,CYTb5,and UDPGT(P<0.05).In the 150 mg/L ATR group,GGT content,peroxide levels(as indicated by malondialdehyde),and CYP1A2 expression were significantly increased(P<0.01),while GSH content was significantly decreased(P<0.05),and hepatocyte injury and mitochondrial vacuolation were more serious when compared to control and 1.5 mg/L groups.Conclusions In a mouse model of low-dose ATR liver injury,both 1.5 mg/L and 150 mg/L ATR exposure induced liver injury in mice,with 150 mg/L ATR inducing the maximum metabolic toxicity in the liver after 63 days.

关键词

莠去津/饮用水/肝损伤/动物模型

Key words

atrazine/drinking water/liver injury/animal model

分类

医药卫生

引用本文复制引用

朱玉,苏莹实,刘溪,何宝国,秦嫘..低剂量莠去津暴露饮用水诱导小鼠肝损伤模型的建立及验证[J].中国比较医学杂志,2024,34(6):73-81,9.

基金项目

黑龙江省教育厅项目(2018-KYYWF-0109) (2018-KYYWF-0109)

"新时代龙江优秀硕士、博士学位论文"资助项目(LJYXL2023-066) (LJYXL2023-066)

齐齐哈尔医学科学院项目(QMSI2023B-18)o (QMSI2023B-18)

中国比较医学杂志

OA北大核心CSTPCD

1671-7856

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