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植物乳杆菌dfa1通过调节炎症和肠道微生物群来减轻高碳水化合物饮食引起的肥胖。

Lactiplantibacillus plantarum dfa1 reduces obesity caused by a high carbohydrate diet by modulating inflammation and gut microbiota.

作者信息

Ondee Thunnicha, Pongpirul Krit, Wongsaroj Lampet, Senaprom Sayamon, Wattanaphansak Suphot, Leelahavanichkul Asada

机构信息

Department of Preventive and Social Medicine, Faculty of Medicine, Chulalongkorn University, Bangkok, 10330, Thailand.

Center of Excellence in Preventive and Integrative Medicine (CE-PIM), Faculty of Medicine, Chulalongkorn University, Bangkok, 10330, Thailand.

出版信息

Sci Rep. 2025 Jul 10;15(1):24801. doi: 10.1038/s41598-025-10435-x.

Abstract

Given the potential of probiotics to counteract obesity induced by high glucose diets (HGD) and the beneficial effects of high-fiber diets, this study explored the impact of Lactiplantibacillus plantarum dfa1 (Lp dfa1) in mice consuming modified diets, including a unique high-carbohydrate biscuit diet (HBD) featuring Prachuap Khiri Khan's Pineapple Cheese Cake Biscuit for its rich fiber content. Notably, the fruit-derived soluble fiber HBD might have a synbiotic effect (the enhanced beneficial bacteria in the gut) different from HGD. in The standard mouse diet (RD) with a carbohydrate: protein: fat (C: P:F) ratio of 56:13:31 served as the base, which was then modified with either glucose to form the HGD (C: P:F at 60:25:15) or blended with the high-fiber dessert to create the HBD (C: P:F at 70:9:21). Over 12 weeks, mice were fed HGD or HBD with and without daily oral administration of Lp dfa1 at 1 × 10 CFU. This study aimed to assess the effects on obesity indicators (weight gain, lipid profiles, fat deposition), prediabetes markers (fasting glucose, insulin, oral glucose tolerance test, and Homeostatic Model Assessment for Insulin Resistance (HOMA-IR)), intestinal health (FITC-dextran assay for enterocyte injury, serum cytokines TNF-α, IL-10, and IL-6), and liver health (enzymes, weight, histology, carbohydrate and fat components, and oxidative stress). Both HGD and HBD induced similar obesity metrics, prediabetic conditions, enterocyte injury, altered serum cytokines, and liver damage. Remarkably, Lp dfa1 administration mitigated these adverse effects with an elevation in fecal short-chain fatty acids. Microbiome analysis revealed diet-induced dysbiosis, with a notable difference between HGD and HBD impacts, particularly in the Fermicutes/Bacteroides ratio and Akkermansia spp. abundance, which was significantly elevated in the HBD + Lp group. Actinomycota with a lower Proteobacteria in HBD compared with HGD group indicate the possible different impacts between the mixed sugar with fruit-derived soluble fiber versus pure glucose. Interestingly, Lp dfa1 elevated Akkermansia spp. (a well-known beneficial probiotic against obesity) only in mice with HBD but not HGD, despite an obesity attenuation by Lp dfa1 in both HGD and HBD groups, implying the different anti-obesity mechanisms. In vitro experiments revealed Lp dfa1's supernatant reduced inflammation in Caco-2 and HepG2 cell lines, evidenced by improved transepithelial electrical resistance (TEER), expression of occludin-1 (a tight junction molecule), decreased inflammatory mediators (NF-κB, TNF-α, IL-8, IL-6, and IL-10), and elevated mucin gene. Conclusively, Lp dfa1 demonstrates a dual mechanism in preventing sugar-induced intestinal injury and supporting metabolic health: direct cellular protection and microbiome modulation. These findings highlight the additive effects of Lp dfa1 and high-fiber diets, particularly emphasizing the Pineapple Cheese Cake Biscuit-based diet's role in enhancing gut microbiota and addressing diet-induced health issues.

摘要

鉴于益生菌具有对抗高糖饮食(HGD)诱导的肥胖的潜力以及高纤维饮食的有益作用,本研究探讨了植物乳杆菌dfa1(Lp dfa1)对食用改良饮食的小鼠的影响,其中包括一种独特的高碳水化合物饼干饮食(HBD),该饮食以巴蜀府的菠萝芝士蛋糕饼干为特色,因其富含纤维。值得注意的是,源自水果的可溶性纤维HBD可能具有与HGD不同的合生元效应(肠道中有益细菌的增加)。以碳水化合物:蛋白质:脂肪(C:P:F)比例为56:13:31的标准小鼠饮食(RD)为基础,然后用葡萄糖进行改良以形成HGD(C:P:F为60:25:15),或与高纤维甜点混合以创建HBD(C:P:F为70:9:21)。在12周的时间里,给小鼠喂食HGD或HBD,并每日口服1×10 CFU的Lp dfa1或不口服。本研究旨在评估对肥胖指标(体重增加、血脂谱、脂肪沉积)、糖尿病前期标志物(空腹血糖、胰岛素、口服葡萄糖耐量试验和胰岛素抵抗稳态模型评估(HOMA-IR))、肠道健康(用于肠细胞损伤的异硫氰酸荧光素-葡聚糖测定、血清细胞因子TNF-α、IL-10和IL-6)以及肝脏健康(酶、重量、组织学、碳水化合物和脂肪成分以及氧化应激)的影响。HGD和HBD均诱导了相似的肥胖指标、糖尿病前期状况、肠细胞损伤、血清细胞因子改变和肝脏损伤。值得注意的是,给予Lp dfa1可减轻这些不良反应,同时粪便短链脂肪酸增加。微生物组分析显示饮食诱导的生态失调HGD和HBD的影响存在显著差异,特别是在厚壁菌门/拟杆菌门比例和阿克曼氏菌属丰度方面,在HBD + Lp组中显著升高。与HGD组相比,HBD中放线菌门含量较低而变形菌门含量较低,这表明含有水果来源可溶性纤维的混合糖与纯葡萄糖之间可能存在不同的影响。有趣的是,尽管Lp dfa1在HGD和HBD组中均减轻了肥胖,但Lp dfa1仅在HBD小鼠中而非HGD小鼠中提高了阿克曼氏菌属(一种著名的抗肥胖有益益生菌)的丰度,这意味着不同的抗肥胖机制。体外实验表明,Lp dfa1的上清液可降低Caco-2和HepG2细胞系中的炎症,这通过改善跨上皮电阻(TEER)、闭合蛋白-1(一种紧密连接分子)的表达、减少炎症介质(NF-κB、TNF-α、IL-8、IL-6和IL-10)以及提高粘蛋白基因得以证明。总之,Lp dfa1在预防糖诱导的肠道损伤和支持代谢健康方面表现出双重机制:直接的细胞保护和微生物组调节。这些发现突出了Lp dfa1和高纤维饮食的相加作用,特别强调了基于菠萝芝士蛋糕饼干的饮食在增强肠道微生物群和解决饮食诱导的健康问题方面的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/415d/12241623/dae88c6574e5/41598_2025_10435_Fig1_HTML.jpg

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