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三叶苷,一种天然存在的食品添加剂,可改善小鼠力竭运动诱导的疲劳:与Nrf2/ARE/铁死亡信号通路有关。

Trilobatin, a Naturally Occurring Food Additive, Ameliorates Exhaustive Exercise-Induced Fatigue in Mice: Involvement of Nrf2/ARE/Ferroptosis Signaling Pathway.

作者信息

Xiao Ran, Wei Yu, Zhang Yueping, Xu Fan, Ma Congjian, Gong Qihai, Gao Jianmei, Xu Yingshu

机构信息

School of Pharmacy, Zunyi Medical University, Zunyi, China.

Key Laboratory of Basic Pharmacology of Ministry of Education and Joint International Research Laboratory of Ethnomedicine of Ministry of Education, Zunyi Medical University, Zunyi, China.

出版信息

Front Pharmacol. 2022 Jun 24;13:913367. doi: 10.3389/fphar.2022.913367. eCollection 2022.

DOI:10.3389/fphar.2022.913367
PMID:35814232
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9263197/
Abstract

Nrf2-mediated oxidative stress is a promising target of exhaustive exercise-induced fatigue (EEIF). Trilobatin (TLB) is a naturally occurring food additive with antioxidant effect and Nrf2 activation potency. The present study aimed to investigate the effect of TLB on EEIF and elucidate its underlying mechanism. Our results showed that TLB exerted potent anti-EEIF effect, as reflected by the rope climbing test and exhaustive swimming test. Moreover, TLB also effectively reduced the levels of lactate, creatine kinase, and blood urea nitrogen, and increased liver glycogen and skeletal muscle glycogen in mice after EEIF insult. Additionally, TLB also balanced the redox status as evidenced by decreasing the generation of reactive oxygen species and improving the antioxidant enzyme activities including superoxide dismutase, catalase, and glutathione peroxidase, as well as the level of glutathione both in the tissue of muscle and myocardium. Furthermore, TLB promoted nuclear factor erythroid 2-related factor 2 (Nrf2) from the cytoplasm to the nucleus, and upregulated its downstream antioxidant response element (ARE) including quinone oxidoreductase-1 and heme oxygenase-1. Intriguingly, TLB also upregulated the GPx4 protein expression and reduced iron overload in mice after EEIF insult. Encouragingly, the beneficial effect of TLB on EEIF-induced oxidative stress and ferroptosis were substantially abolished in Nrf2-deficient mice. In conclusion, our findings demonstrate, for the first time, that TLB alleviates EEIF-induced oxidative stress through mediating Nrf2/ARE/ferroptosis axis.

摘要

Nrf2介导的氧化应激是力竭运动诱导疲劳(EEIF)的一个有前景的靶点。三叶苷(TLB)是一种具有抗氧化作用和Nrf2激活能力的天然食品添加剂。本研究旨在探讨TLB对EEIF的影响并阐明其潜在机制。我们的结果表明,TLB发挥了强大的抗EEIF作用,这在爬绳试验和力竭游泳试验中得到了体现。此外,TLB还有效降低了力竭运动损伤后小鼠体内乳酸、肌酸激酶和血尿素氮的水平,并增加了肝糖原和骨骼肌糖原。此外,TLB还平衡了氧化还原状态,表现为减少活性氧的生成,提高抗氧化酶活性,包括超氧化物歧化酶、过氧化氢酶和谷胱甘肽过氧化物酶,以及肌肉和心肌组织中的谷胱甘肽水平。此外,TLB促进核因子红细胞2相关因子2(Nrf2)从细胞质转移到细胞核,并上调其下游抗氧化反应元件(ARE),包括醌氧化还原酶-1和血红素加氧酶-1。有趣的是,TLB还上调了力竭运动损伤后小鼠体内GPx4蛋白的表达并减少了铁过载。令人鼓舞的是,在Nrf2基因敲除小鼠中,TLB对EEIF诱导的氧化应激和铁死亡的有益作用基本消失。总之,我们的研究结果首次表明,TLB通过介导Nrf2/ARE/铁死亡轴减轻EEIF诱导的氧化应激。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ff82/9263197/b8335cfa929e/fphar-13-913367-g008.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ff82/9263197/b8335cfa929e/fphar-13-913367-g008.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ff82/9263197/d4df56477cd0/fphar-13-913367-g002.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ff82/9263197/654fe300db50/fphar-13-913367-g004.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ff82/9263197/387045c2ac69/fphar-13-913367-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ff82/9263197/00ed83552e51/fphar-13-913367-g007.jpg
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