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提取物对乙酰氨基酚诱导的肝损伤的保护作用。

Protective Effects of Extract against Acetaminophen-Induced Liver Injury.

作者信息

Lee Yea-Lim, Lee Ji-Yun, Park Joo-Woong, Lee Jin, Lee Hyun-Hoo, Lee Dae-Hee

机构信息

Nbio, Inc., Gangneung 25457, Republic of Korea.

Biostream Co., Ltd., Suwon 10442, Republic of Korea.

出版信息

J Microbiol Biotechnol. 2024 Dec 28;34(12):2675-2862. doi: 10.4014/jmb.2409.09061. Epub 2024 Oct 25.

DOI:10.4014/jmb.2409.09061
PMID:39473023
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11729533/
Abstract

Acetaminophen (APAP) is a well-known analgesic used globally. Generally, APAP has been proven to be safe and effective at therapeutic doses; however, it can cause serious liver damage when administered at high levels. We prepared extract (CFE) using the seaweed and confirmed that the CFE contains a substance called Loliolide with antioxidant activity. We performed the present study to determine whether CFE protects HEPG2 cells and BALB/c mice from oxidative stress-induced liver damage. We confirmed that CFE and Loliolide were non-cytotoxic and protected against liver damage by reducing the activities of ALT and AST, which were increased by APAP treatment, and that CFE reduced the mRNA expression of inflammatory cytokines TNF-α and IL-6 and inhibited the phosphorylation of ERK and p38 in HEPG2 cells as determined by RT-PCR and Western blot analyses. Furthermore, the TNF-α and IL-6 levels, which were increased after APAP treatment in BALB/c mice, decreased after CFE treatment. Therefore, we demonstrated that CFE exerts a protective effect against APAP-induced liver injury by suppressing the inflammatory response through anti-inflammatory activity. Our findings provide new perspectives for developing functional foods that utilize seaweeds to improve liver function.

摘要

对乙酰氨基酚(APAP)是一种在全球范围内广泛使用的知名镇痛药。一般来说,已证明APAP在治疗剂量下是安全有效的;然而,高剂量使用时它会导致严重的肝损伤。我们用这种海藻制备了提取物(CFE),并证实CFE含有一种具有抗氧化活性的物质叫洛利内酯。我们进行本研究以确定CFE是否能保护HEPG2细胞和BALB/c小鼠免受氧化应激诱导的肝损伤。我们证实CFE和洛利内酯无细胞毒性,通过降低APAP处理后升高的ALT和AST活性来保护肝脏免受损伤,并且通过RT-PCR和蛋白质印迹分析确定,CFE降低了HEPG2细胞中炎性细胞因子TNF-α和IL-6的mRNA表达,并抑制了ERK和p38的磷酸化。此外,APAP处理后BALB/c小鼠中升高的TNF-α和IL-6水平在CFE处理后降低。因此,我们证明CFE通过抗炎活性抑制炎症反应,对APAP诱导的肝损伤发挥保护作用。我们的研究结果为开发利用海藻改善肝功能的功能性食品提供了新的视角。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3d3d/11729533/cbf2fe19f04d/jmb-34-12-2675-f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3d3d/11729533/bedb7c991e0f/jmb-34-12-2675-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3d3d/11729533/0f46bfeef39d/jmb-34-12-2675-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3d3d/11729533/94a2dcdd9285/jmb-34-12-2675-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3d3d/11729533/c12d084be0e9/jmb-34-12-2675-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3d3d/11729533/6e0a540945d0/jmb-34-12-2675-f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3d3d/11729533/cbf2fe19f04d/jmb-34-12-2675-f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3d3d/11729533/bedb7c991e0f/jmb-34-12-2675-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3d3d/11729533/0f46bfeef39d/jmb-34-12-2675-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3d3d/11729533/94a2dcdd9285/jmb-34-12-2675-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3d3d/11729533/c12d084be0e9/jmb-34-12-2675-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3d3d/11729533/6e0a540945d0/jmb-34-12-2675-f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3d3d/11729533/cbf2fe19f04d/jmb-34-12-2675-f6.jpg

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本文引用的文献

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Bacillus amyloliquefaciens B10 can alleviate liver apoptosis and oxidative stress induced by aflatoxin B1.
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