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一种用于评估新型益生菌-多廿烷醇组合抗肥胖潜力的体外肠-肝-脂肪轴模型

An In Vitro Gut-Liver-Adipose Axis Model to Evaluate the Anti-Obesity Potential of a Novel Probiotic-Polycosanol Combination.

作者信息

Mulè Simone, Galla Rebecca, Parini Francesca, Botta Mattia, Ferrari Sara, Uberti Francesca

机构信息

Department for Sustainable Development and Ecological Transition, University of Piemonte Orientale (UPO), 13100 Vercelli, Italy.

Noivita Srls, Spin Off, University of Piemonte Orientale (UPO), Via Solaroli 17, 28100 Novara, Italy.

出版信息

Foods. 2025 Jun 5;14(11):2003. doi: 10.3390/foods14112003.

DOI:10.3390/foods14112003
PMID:40509530
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12154259/
Abstract

The gut-liver-adipose axis plays a pivotal role in metabolic regulation, and its dysregulation contributes to obesity and metabolic syndrome. Probiotics and polycosanol have shown potential in modulating gut barrier integrity, lipid metabolism, and inflammation. This study aimed to evaluate their combined effects using an in vitro model of the gut-liver-adipose axis. Transwell system was used to recreate the interaction between intestinal (CaCo-2), hepatic (HepG2), and adipose (3T3-L1) cells. Cells were treated with GM-25, GM-21, GM-28, and polycosanols. The effects were assessed by analyzing intestinal barrier integrity (TEER, tight junction proteins), hepatic and adipose lipid accumulation (Oil Red O staining), oxidative stress (ROS production, lipid peroxidation), inflammation (TNF-α) and lipid metabolism (CD36, PPARγ, AMPK and SREBP-1 levels). Probiotics and polycosanols improved intestinal integrity, increased butyrate production, and reduced ROS levels. Hepatic lipid accumulation was significantly decreased, with enhanced PPARγ and AMPK activation. In adipocytes, probiotic-polycosanols treatment suppressed SREBP-1 expression, enhanced lipid oxidation, and promoted UCP1 and PGC-1α expression, suggesting activation of thermogenic pathways. These findings underline a possible biological relevance of probiotics and polycosanols in modulating metabolic pathways, improving gut barrier integrity, and reducing inflammation, supporting their role as functional ingredients for metabolic health.

摘要

肠-肝-脂肪轴在代谢调节中起关键作用,其失调会导致肥胖和代谢综合征。益生菌和多廿烷醇已显示出在调节肠道屏障完整性、脂质代谢和炎症方面的潜力。本研究旨在使用肠-肝-脂肪轴的体外模型评估它们的联合作用。采用Transwell系统重建肠(CaCo-2)、肝(HepG2)和脂肪(3T3-L1)细胞之间的相互作用。细胞用GM-25、GM-21、GM-28和多廿烷醇处理。通过分析肠道屏障完整性(跨上皮电阻、紧密连接蛋白)、肝和脂肪脂质积累(油红O染色)、氧化应激(活性氧产生、脂质过氧化)、炎症(肿瘤坏死因子-α)和脂质代谢(CD36、过氧化物酶体增殖物激活受体γ、腺苷酸活化蛋白激酶和固醇调节元件结合蛋白-1水平)来评估其作用。益生菌和多廿烷醇改善了肠道完整性,增加了丁酸盐产生,并降低了活性氧水平。肝脂质积累显著减少,同时过氧化物酶体增殖物激活受体γ和腺苷酸活化蛋白激酶的激活增强。在脂肪细胞中,益生菌-多廿烷醇处理抑制了固醇调节元件结合蛋白-1的表达,增强了脂质氧化,并促进了解偶联蛋白1和过氧化物酶体增殖物激活受体γ共激活因子1α的表达,表明产热途径被激活。这些发现强调了益生菌和多廿烷醇在调节代谢途径、改善肠道屏障完整性和减轻炎症方面可能具有的生物学相关性,支持了它们作为代谢健康功能成分的作用。

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本文引用的文献

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Front Pharmacol. 2025 Apr 14;16:1546456. doi: 10.3389/fphar.2025.1546456. eCollection 2025.
2
Effects of Quercetin Metabolites on Glucose-Dependent Lipid Accumulation in 3T3-L1 Adipocytes.槲皮素代谢物对3T3-L1脂肪细胞中葡萄糖依赖性脂质积累的影响。
Mol Nutr Food Res. 2025 Apr 21:e70070. doi: 10.1002/mnfr.70070.
3
Comparative analysis of β-Estradiol and testosterone on lipid droplet accumulation, and regulatory protein expression in palmitate/oleate-induced fatty HepG2 cells.
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BMC Gastroenterol. 2025 Apr 16;25(1):263. doi: 10.1186/s12876-025-03863-6.
4
Understanding the Link Between Sterol Regulatory Element Binding Protein (SREBPs) and Metabolic Dysfunction Associated Steatotic Liver Disease (MASLD).了解固醇调节元件结合蛋白(SREBPs)与代谢功能障碍相关脂肪性肝病(MASLD)之间的联系。
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5
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Free Radic Res. 2025 Jan;59(1):86-101. doi: 10.1080/10715762.2024.2449457. Epub 2025 Jan 8.
6
Metabolomic Hallmarks of Obesity and Metabolic Dysfunction-Associated Steatotic Liver Disease.肥胖及代谢功能障碍相关脂肪性肝病的代谢组学特征
Int J Mol Sci. 2024 Nov 28;25(23):12809. doi: 10.3390/ijms252312809.
7
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8
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