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镉诱导内质网应激及其对大鼠肾脏 Nrf2 信号通路的调节。

Induction of Endoplasmic Reticulum Stress by Cadmium and Its Regulation on Nrf2 Signaling Pathway in Kidneys of Rats.

机构信息

School of Public Health, Guangdong Pharmaceutical University, Guangzhou 510310, Guangdong, China.

Bao'an Center for Disease Control and Prevention of Shenzhen, Shenzhen 518101, Guangdong, China.

出版信息

Biomed Environ Sci. 2019 Jan;32(1):1-10. doi: 10.3967/bes2019.001.

Abstract

OBJECTIVE

This study was conducted to investigate the regulation of endoplasmic reticulum stress on Nrf2 signaling pathway in the kidneys of rats.

METHODS

Rats were divided into twelve groups of six animals each. Some groups were pre-administered with bacitracin or tauroursodeoxycholic acid (TUDCA), and all of them were treated with 5-20 μmol/kg cadmium (Cd) for 48 h. The oxidative stress levels were analyzed using kits. The mRNA and protein expression levels of endoplasmic reticulum stress-related factors and Nrf2 signaling pathway-related factors were determined using RT-PCR and western blot.

RESULTS

Cd exposure resulted in oxidative stress in the kidneys of rats and upregulated the expression of endoplasmic reticulum stress (ERS)-related factors and Nrf2 signaling pathway-related factors, especially at doses of 10 and 20 μmol/kg Cd, and the expression changes were particularly obvious. Moreover, after pretreatment with bacitracin, Cd upregulated the expression of ERS-related factors to a certain extent and, at higher doses, increased the mRNA expression of Nrf2. After pretreatment with TUDCA, Cd reduced the level of ERS to a certain extent; however, at these doses, there were no significant changes in the expression of Nrf2.

CONCLUSION

Cadmium can result in ERS and oxidative stress in the kidneys of rats, activate Nrf2, and upregulate the transcriptional expression of phase II detoxification enzymes under these experimental conditions. ERS has a positive regulation effect on Nrf2 signaling pathway but has little effect on the negative regulation of Nrf2 signaling pathway in cadmium toxicity.

摘要

目的

本研究旨在探讨内质网应激对大鼠肾脏中 Nrf2 信号通路的调节作用。

方法

将大鼠分为 12 组,每组 6 只。部分组给予杆菌肽或牛磺熊脱氧胆酸(TUDCA)预处理,所有组均给予 5-20 μmol/kg 镉(Cd)处理 48 h。采用试剂盒分析氧化应激水平。采用 RT-PCR 和 Western blot 法测定内质网应激相关因子和 Nrf2 信号通路相关因子的 mRNA 和蛋白表达水平。

结果

Cd 暴露导致大鼠肾脏发生氧化应激,上调内质网应激(ERS)相关因子和 Nrf2 信号通路相关因子的表达,尤其在 10 和 20 μmol/kg Cd 剂量时表达变化尤为明显。此外,杆菌肽预处理后,Cd 在一定程度上上调 ERS 相关因子的表达,且在高剂量时增加 Nrf2 的 mRNA 表达。TUDCA 预处理后,Cd 在一定程度上降低 ERS 水平;但在这些剂量下,Nrf2 的表达没有明显变化。

结论

在这些实验条件下,Cd 可导致大鼠肾脏发生 ERS 和氧化应激,激活 Nrf2,并上调 II 相解毒酶的转录表达。ERS 对 Nrf2 信号通路具有正调控作用,但对 Cd 毒性中 Nrf2 信号通路的负调控作用较小。

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