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发酵汁通过调控 AML-12 细胞 NRF2-AMPK 信号通路对乙醇诱导的肝细胞损伤的保护作用。

Protective effects of fermented juice against ethanol‑induced hepatocyte injury by regulating the NRF2‑AMPK signaling pathway in AML‑12 cells.

机构信息

School of Public Health, Zhejiang Chinese Medical University, Hangzhou, Zhejiang 310053, P.R. China.

School of Food Science and Engineering, Zhejiang University of Technology, Hangzhou, Zhejiang 310014, P.R. China.

出版信息

Mol Med Rep. 2024 Oct;30(4). doi: 10.3892/mmr.2024.13298. Epub 2024 Aug 2.

DOI:10.3892/mmr.2024.13298
PMID:39092554
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11332318/
Abstract

Alcohol‑related liver disease (ALD) is a major health concern worldwide. In recent years, there has been growing interest in natural products and functional foods for preventing and treating ALD due to their potential antioxidant and hepatoprotective properties. , known for its rich content of bioactive compounds, has demonstrated promising health benefits, including anti‑inflammatory and antioxidant effects. Fermentation has been utilized as a strategy to enhance the bioavailability and efficacy of natural products. In the present study, using a mixture of , lotus leaf extract and grape seed proanthocyanidins fermented by HH‑LP56, a novel fermented (FRRT) juice was discovered that can prevent and regulate ethanol‑induced liver cell damage. Following fermentation, the pH was significantly decreased, and the content of VC and superoxide dismutase (SOD) were significantly increased, along with a noticeable enhancement in hydroxyl and 2,2‑diphenyl‑1‑picrylhydrazyl free radical scavenging abilities. Alpha Mouse liver 12 cells were exposed to ethanol for 24 h to establish an liver cell injury model. The present study evaluated the effects of FRRT on cell damage, lipid accumulation and oxidative stress markers. The results revealed that FRRT pretreatment (cells were pre‑treated with 2.5 and 5 mg/ml FRRT for 2 h) significantly reduced lipid accumulation and oxidative stress in liver cells. Mechanistically, FRRT regulated lipid metabolism by influencing key genes and proteins, such as AMP‑activated protein kinase, sterol regulatory element binding transcription factor 1 and Stearyl‑CoA desaturase‑1. Furthermore, FRRT enhanced antioxidant activity by increasing SOD activity, glutathione and catalase levels, while reducing reactive oxygen species and malondialdehyde levels. It also reversed the expression changes of ethanol‑induced oxidative stress‑related genes and proteins. In conclusion, a novel functional food ingredient may have been discovered with extensive potential applications. These findings indicated that FRRT has antioxidant properties and potential therapeutic benefits in addressing ethanol‑induced liver cell damage through its effects on liver lipid metabolism and oxidative stress.

摘要

酒精性肝病(ALD)是全球范围内的一个主要健康问题。近年来,由于天然产物和功能性食品具有潜在的抗氧化和肝保护特性,因此人们对其预防和治疗 ALD 的兴趣日益浓厚。[莲]因其丰富的生物活性化合物含量而闻名,具有抗炎和抗氧化作用。发酵已被用作提高天然产物生物利用度和功效的策略。在本研究中,使用[莲]、荷叶提取物和葡萄籽原花青素的混合物,由 HH-LP56 发酵,发现了一种新型发酵[莲](FRRT)汁,可预防和调节乙醇诱导的肝细胞损伤。发酵后,pH 值显著降低,VC 和超氧化物歧化酶(SOD)的含量显著增加,同时羟基和 2,2-二苯基-1-苦基肼自由基清除能力明显增强。将α Mouse liver 12 细胞暴露于乙醇中 24 h 以建立肝细胞损伤模型。本研究评估了 FRRT 对细胞损伤、脂质积累和氧化应激标志物的影响。结果表明,FRRT 预处理(细胞用 2.5 和 5 mg/ml FRRT 预处理 2 h)显著减少了肝细胞中的脂质积累和氧化应激。机制上,FRRT 通过影响关键基因和蛋白质,如 AMP 激活蛋白激酶、固醇调节元件结合转录因子 1 和硬脂酰辅酶 A 去饱和酶-1,调节脂质代谢。此外,FRRT 通过增加 SOD 活性、谷胱甘肽和过氧化氢酶水平,同时降低活性氧和丙二醛水平来增强抗氧化活性。它还逆转了乙醇诱导的氧化应激相关基因和蛋白质的表达变化。总之,一种新的功能性食品成分可能已经被发现,具有广泛的应用潜力。这些发现表明,FRRT 具有抗氧化特性,并通过其对肝脂质代谢和氧化应激的影响,在解决乙醇诱导的肝细胞损伤方面具有潜在的治疗益处。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec2c/11332318/59efe080cf76/mmr-30-04-13298-g07.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec2c/11332318/7db21993fe2e/mmr-30-04-13298-g01.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec2c/11332318/eef219ee468c/mmr-30-04-13298-g06.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec2c/11332318/59efe080cf76/mmr-30-04-13298-g07.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec2c/11332318/7db21993fe2e/mmr-30-04-13298-g01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec2c/11332318/3db777eeb019/mmr-30-04-13298-g02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec2c/11332318/0e0ad51337f7/mmr-30-04-13298-g03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec2c/11332318/7e7435c16d7b/mmr-30-04-13298-g04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec2c/11332318/72e48c41ee56/mmr-30-04-13298-g05.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec2c/11332318/eef219ee468c/mmr-30-04-13298-g06.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec2c/11332318/59efe080cf76/mmr-30-04-13298-g07.jpg

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