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生育三烯酚激活 Nrf2 核转位并增加小鼠肝脏的抗氧化相关肝保护机制。

Tocotrienols Activate Nrf2 Nuclear Translocation and Increase the Antioxidant- Related Hepatoprotective Mechanism in Mice Liver.

机构信息

Department of Pharmacology, Faculty of Medicine, Universiti Kebangsaan Malaysia, Jalan Yaacob Latif, Bandar Tun Razak, 56000 Cheras, Kuala Lumpur, Malaysia.

出版信息

Curr Pharm Biotechnol. 2021;22(8):1085-1098. doi: 10.2174/1389201021666200928095950.

DOI:10.2174/1389201021666200928095950
PMID:32988349
Abstract

BACKGROUND

The most common preparation of tocotrienols is the Tocotrienol-Rich Fraction (TRF). This study aimed to investigate whether TRF induced liver Nrf2 nuclear translocation and influenced the expression of Nrf2-regulated genes.

METHODS

In the Nrf2 induction study, mice were divided into control, 2000 mg/kg TRF and diethyl maleate treated groups. After acute treatment, mice were sacrificed at specific time points. Liver nuclear extracts were prepared and Nrf2 nuclear translocation was detected through Western blotting. To determine the effect of increasing doses of TRF on the extent of liver nuclear Nrf2 translocation and its implication on the expression levels of several Nrf2-regulated genes, mice were divided into 5 groups (control, 200, 500 and 1000 mg/kg TRF, and butylated hydroxyanisole-treated groups). After 14 days, mice were sacrificed and liver RNA was extracted for qPCR assay.

RESULTS

2000 mg/kg TRF administration initiated Nrf2 nuclear translocation within 30 min, reached a maximum level of around 1 h and dropped to half-maximal levels by 24 h. Incremental doses of TRF resulted in dose-dependent increases in liver Nrf2 nuclear levels, along with concomitant dosedependent increases in the expressions of Nrf2-regulated genes.

CONCLUSION

TRF activated the liver Nrf2 pathway resulting in increased expression of Nrf2-regulated cytoprotective genes.

摘要

背景

生育三烯酚最常见的制剂是生育三烯酚浓缩物(TRF)。本研究旨在探讨 TRF 是否诱导肝脏 Nrf2 核转位并影响 Nrf2 调节基因的表达。

方法

在 Nrf2 诱导研究中,将小鼠分为对照组、2000mg/kg TRF 组和马来酸二乙酯处理组。急性处理后,在特定时间点处死小鼠。制备肝核提取物,并通过 Western blot 检测 Nrf2 核转位。为了确定增加 TRF 剂量对肝核 Nrf2 转位程度的影响及其对几种 Nrf2 调节基因表达水平的影响,将小鼠分为 5 组(对照组、200、500 和 1000mg/kg TRF 组和丁基羟基茴香醚处理组)。14 天后,处死小鼠并提取肝 RNA 进行 qPCR 分析。

结果

2000mg/kg TRF 给药在 30 分钟内引发 Nrf2 核转位,在 1 小时左右达到最大水平,并在 24 小时降至半最大水平。递增剂量的 TRF 导致肝 Nrf2 核水平呈剂量依赖性增加,同时 Nrf2 调节基因的表达也呈剂量依赖性增加。

结论

TRF 激活了肝脏 Nrf2 通路,导致 Nrf2 调节的细胞保护基因表达增加。

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