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可可多酚可改变粪便微生物群,但在喂食健康或西式基础饮食的小鼠中不能减轻结肠炎。

Cocoa Polyphenols Alter the Fecal Microbiome Without Mitigating Colitis in Mice Fed Healthy or Western Basal Diets.

作者信息

Stewart Eliza C, Almatani Mohammed F, Hayden Marcus, Rompato Giovanni, Case Jeremy, Rice Samuel, Hintze Korry J, Benninghoff Abby D

机构信息

Department of Animal, Dairy and Veterinary Sciences, Utah State University, 4815 Old Main Hill, Logan, UT 84322, USA.

Department of Pharmacology, College of Pharmacy, King Khalid University, Al Fara, Abha 62223, Saudi Arabia.

出版信息

Nutrients. 2025 Jul 29;17(15):2482. doi: 10.3390/nu17152482.

DOI:10.3390/nu17152482
PMID:40806068
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12348170/
Abstract

: Chronic inflammation and Western-style diets elevate colorectal cancer (CRC) risk, particularly in individuals with colitis, a feature of inflammatory bowel disease (IBD). Diets rich in polyphenol-containing functional foods, such as cocoa, may reduce gut inflammation and modulate the gut microbiome. This study investigated the impact of cocoa polyphenol (CP) supplementation on inflammation and microbiome composition in mice with colitis, fed either a healthy or Western diet, before, during, and after the onset of disease. We hypothesized that CPs would attenuate inflammation and promote distinct shifts in the microbiome, especially in the context of a Western diet. : A 2 × 2 factorial design tested the effects of the basal diet (AIN93G vs. total Western diet [TWD]) and CP supplementation (2.6% / CocoaVia™ Cardio Health Powder). Inflammation was induced using the AOM/DSS model of colitis. : CP supplementation did not reduce the severity of colitis, as measured by disease activity index or histopathology. CPs did not alter gene expression in healthy tissue or suppress the colitis-associated pro-inflammatory transcriptional profile in either of the two diet groups. However, fecal microbiome composition shifted significantly with CPs before colitis induction, with persistent effects on several rare taxa during colitis and recovery. : CP supplementation did not mitigate inflammation or mucosal injury at the tissue level, nor did it affect the expression of immune-related genes. While CPs altered microbiome composition, most notably in healthy mice before colitis, these shifts did not correspond to changes in inflammatory signaling. Basal diet remained the primary determinant of inflammation, mucosal damage, and colitis severity in this model.

摘要

慢性炎症和西式饮食会增加结直肠癌(CRC)风险,尤其是在患有结肠炎的个体中,结肠炎是炎症性肠病(IBD)的一个特征。富含含多酚功能食品(如可可)的饮食可能会减轻肠道炎症并调节肠道微生物群。本研究调查了补充可可多酚(CP)对结肠炎小鼠炎症和微生物群组成的影响,这些小鼠在疾病发作前、发作期间和发作后分别喂食健康饮食或西式饮食。我们假设CP会减轻炎症并促进微生物群的明显变化,尤其是在西式饮食的情况下。:采用2×2析因设计测试基础饮食(AIN93G与全西式饮食 [TWD])和CP补充(2.6% / CocoaVia™ 心脏健康粉)的效果。使用AOM/DSS结肠炎模型诱导炎症。:通过疾病活动指数或组织病理学测量,补充CP并未降低结肠炎的严重程度。CP在两个饮食组中均未改变健康组织中的基因表达或抑制与结肠炎相关的促炎转录谱。然而,在诱导结肠炎之前,粪便微生物群组成随CP显著变化,在结肠炎和恢复期间对几种稀有分类群有持续影响。:补充CP在组织水平上并未减轻炎症或黏膜损伤,也未影响免疫相关基因的表达。虽然CP改变了微生物群组成(最明显的是在结肠炎前的健康小鼠中),但这些变化与炎症信号的变化并不对应。在该模型中,基础饮食仍然是炎症、黏膜损伤和结肠炎严重程度的主要决定因素。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ea74/12348170/194689ed2a2a/nutrients-17-02482-g010.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ea74/12348170/a8b7be488836/nutrients-17-02482-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ea74/12348170/6be6bf0d156f/nutrients-17-02482-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ea74/12348170/194689ed2a2a/nutrients-17-02482-g010.jpg

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The association between dietary inflammatory potential and risk of total and site-specific colorectal cancer: a systematic review and meta-analysis of observational studies.饮食炎症潜能与总体及特定部位结直肠癌风险之间的关联:观察性研究的系统评价和荟萃分析
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Gut Microbiome and Lipidome Signatures in Irritable Bowel Syndrome Patients from a Low-Income, Food-Desert Area: A Pilot Study.
低收入食物匮乏地区肠易激综合征患者的肠道微生物组和脂质组特征:一项试点研究
Microorganisms. 2023 Oct 6;11(10):2503. doi: 10.3390/microorganisms11102503.
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Dietary Supplementation with a Cocoa-Carob Blend Modulates Gut Microbiota and Prevents Intestinal Oxidative Stress and Barrier Dysfunction in Zucker Diabetic Rats.用可可-角豆混合物进行膳食补充可调节Zucker糖尿病大鼠的肠道微生物群并预防肠道氧化应激和屏障功能障碍。
Antioxidants (Basel). 2023 Jul 29;12(8):1519. doi: 10.3390/antiox12081519.
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