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首页|期刊导航|海南医科大学学报|妊娠期和妊娠哺乳期CdCl2暴露对子代小鼠海马损伤神经毒性影响

妊娠期和妊娠哺乳期CdCl2暴露对子代小鼠海马损伤神经毒性影响

饶文莲 李文学 岑育芳 陈冬顺 刘宝熙 李博雅 兰银材 庞雅琴

海南医科大学学报2026,Vol.32Issue(12):890-899,10.
海南医科大学学报2026,Vol.32Issue(12):890-899,10.DOI:10.13210/j.cnki.jhmu.20250306.003

妊娠期和妊娠哺乳期CdCl2暴露对子代小鼠海马损伤神经毒性影响

Neurotoxic effects of CdCl2 exposure during pregnancy and lactation on hippocampal damage in offspring mice

饶文莲 1李文学 2岑育芳 3陈冬顺 1刘宝熙 3李博雅 4兰银材 4庞雅琴5

作者信息

  • 1. 右江民族医学院医学技术与人工智能学院,广西 百色 533000
  • 2. 广州市疾病预防控制中心毒理与生化检验科,广东 广州 510440
  • 3. 右江民族医学院基础医学院,广西 百色 533000
  • 4. 右江民族医学院公共卫生学院,广西 百色 533000
  • 5. 右江民族医学院医学技术与人工智能学院,广西 百色 533000||广西高校生态铝工业基地环境与人群健康研究重点实验室,广西 百色 533000||右江民族医学院"环境污染与健康风险评价"重点实验室,广西 百色 533000
  • 折叠

摘要

Abstract

Objective:To investigate the neurotoxic effects of CdCl2 exposure during pregnancy and lactation on hippocampal injury in offspring mice.Methods:The pregnant mice were divided into 3 groups:the control group,the 5 mg/kg group and the 10 mg/kg CdCl2 group.The pregnant and lactating mice were respectively administered intragastrically with normal saline,5 mg/kg and 10 mg/kg of CdCl2.The birth status,physical development,histopathological changes and hippocampal cell apoptosis of offspring mice were observed.The brain organ coefficient was calculated.ICP-MS was used to evaluate the changes in cadmium,zinc and iron levels in the brain and blood of PDN1 and PDN30 offspring.qRT-PCR was used to analyze the expression of inflam-matory neurological function-related factors in the hippocampus of PND1 and PND30 offspring.Results:CdCl2 exposure during pregnancy and lactation had no effect on the body weight of PND1,PND30 offspring mice and maternal mice.The brain organ co-efficient of PND1 offspring in the 10 mg/kg group was reduced(P<0.01).CdCl2 exposure will lead to increased PND1 offspring's brain cadmium,and PND30 offspring's brain or blood cadmium,decreased iron and zinc levels(P<0.05).On the 2nd,3rd,4th and 5th days of positioning navigation,the escape latency of PND30 offspring in the 5 mg/kg and 10 mg/kg groups was prolonged compared to the control group(P<0.01);The spatial exploration test data showed that the times of the PND30 offspring in the 5 mg/kg and 10 mg/kg groups crossed the platform,and the target quadrant residence time was reduced(P<0.05).CdCl2 exposure caused different degrees of pathological changes in the CA1 and CA3 regions of the hippocampus of PND30 offspring mice,in-creased apoptosis in the CA1 and DG regions,and no pathological changes were found in the hippocampus of PND1 offspring.Compared to the control group,the mRNA of IL-1β,IL-6,TNF-α,APP,Tau,Ki67,BDNF,GFAP,Nestin,Arg-1,IL-4,and IL-10 in the 5mg/kg and 10mg/kg groups did not show statistically significant differences in the brain of the PND1 offspring(P>0.05);The mRNA expression of IL-1β,IL-6,TNF-α,APP,and Tau was upregulated in the 5 mg/kg or 10 mg/kg groups,and the expression of IL-4,IL-10,Arg-1,Ki67,BDNF,GFAP,and Nestin was downregulated in the hippocampus of the PND30 offspring mice(P<0.05).Conclusion:CdCl2 exposure during pregnancy or lactation proves that a small amount of CdCl2 enters the offspring through the placental glucocorticoid barrier and the blood-brain barrier,and most of it is transferred to the offspring through breast milk,which can cause reduced iron and zinc levels in PND1 and PND30 offspring,as well as damage to hippocampal memory and neurological function in PND30 offspring,and induce brain inflammatory response.

关键词

妊娠期/妊娠哺乳期/CdCl2/海马/神经毒性

Key words

Pregnancy/Pregnancy and Lactation/CdCl2/Hippocampus/Neurotoxicity

分类

医药卫生

引用本文复制引用

饶文莲,李文学,岑育芳,陈冬顺,刘宝熙,李博雅,兰银材,庞雅琴..妊娠期和妊娠哺乳期CdCl2暴露对子代小鼠海马损伤神经毒性影响[J].海南医科大学学报,2026,32(12):890-899,10.

基金项目

This study was supported by the 2024 Innovation Project of Youjiang Medical University for Nationalities Graduate Education(YXCXJH2024001) (YXCXJH2024001)

Guangxi Key R&D Program(2023AB22053) (2023AB22053)

Guangxi Natural Science Foundation Project(2019JJD140011) 2024年右江民族医学院研究生创新计划项目(YXCXJH2024001) (2019JJD140011)

广西重点研发计划(2023AB22053) (2023AB22053)

广西自然科学基金项目(2019JJD140011) (2019JJD140011)

海南医科大学学报

1007-1237

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