碳水化合物负荷饮食与肠道微生物群的相关性:一项系统综述

IF 4.6 3区 生物学 Q2 MICROBIOLOGY
Omar El-Kholy, Lindsey Nichols, Ahmed Adham R. Elsayed, Marc D. Basson
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引用次数: 0

摘要

肠道微生物组对消化、粘膜通透性、代谢、血压和脂质谱有重要影响。这些过程的病理变化导致代谢综合征,这是一个日益严重的人类健康问题,可能在碳水化合物负荷饮食的动物中模拟。我们回顾了碳水化合物负荷饮食对动物肠道微生物组的影响。系统检索了截至2024年9月的五个数据库:Cochrane Library、PubMed、Scopus、Web of Science和VHL。使用sycle的工具评估相关动物研究的偏倚风险。其中包括17项研究,数据来自690多只啮齿动物。碳水化合物负荷饮食改变肠道微生物组成、多样性和比例。高碳水化合物、高脂肪饮食几乎始终与厚壁菌门与拟杆菌门(F/B)比率的增加有关。不同类型的碳水化合物,如果糖、蔗糖,甚至特殊的饮食类型,在影响微生物群和微生物群相关的病理生理、诱导不同的代谢状态和影响血压、肠道结构完整性、免疫调节和其他功能方面差异很大。在喂食时或喂食后加入干预措施,可显著调节这些饮食引起的变化。碳水化合物负荷饮食可以对肠道微生物群和相关生理产生不同的影响。除了以淀粉为基础的饮食外,高脂肪碳水化合物饮食通常会增加脂肪/脂肪比,这一变化与人类肥胖有关。相比之下,低脂碳水化合物饮食不会提高F/B比,而是产生不同的微生物组效应,根据碳水化合物类型和其他影响因素,有有益的也有有害的。进一步的动物和人类研究对于验证和进一步阐明饮食对肠道微生物群的影响至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

The Correlation Between Carbohydrate Loading Diet and Gut Microbiome: A Systematic Review

The Correlation Between Carbohydrate Loading Diet and Gut Microbiome: A Systematic Review

The gut microbiome critically influences digestion, mucosal permeability, metabolism, blood pressure, and lipid profile. Pathological shifts in these processes cause metabolic syndrome, a growing human health concern that may be modeled in animals with carbohydrate-loading diets. We reviewed the effects of carbohydrate-loading diets on the animal gut microbiome. A systematic literature search was performed up to September 2024 on five databases: Cochrane Library, PubMed, Scopus, Web of Science, and VHL. Relevant animal studies were assessed for risk of bias using SYRCLE's tool. Seventeen studies were included, with data from more than 690 rodents. Carbohydrate-loading diets alter the gut microbiome composition, diversity, and ratios. High-carbohydrate, high-fat diets were almost consistently associated with an increased Firmicutes to Bacteroidetes (F/B) ratio. Different types of carbohydrates, such as fructose, sucrose, or even special diet types, vary widely in impacting both the microbiota and microbiota-associated pathophysiology, inducing different metabolic states and affecting blood pressure, gut structural integrity, immunomodulation, and other functions. Interventions added with or after feeding substantially modulated these diet-induced changes. Carbohydrate-loading diets can differentially influence the gut microbiome and associated physiology. High-fat carbohydrate diets, apart from starch-based diets, typically increase the F/B ratio, a shift linked to human obesity. In contrast, low-fat carbohydrate diets do not elevate the F/B ratio but instead produce diverse microbiome effects, ranging from beneficial to harmful, depending on the carbohydrate type and other influencing factors. Further animal and human research is crucial to validate and further illuminate the dietary impact on the gut microbiome.

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来源期刊
MicrobiologyOpen
MicrobiologyOpen MICROBIOLOGY-
CiteScore
8.00
自引率
0.00%
发文量
78
审稿时长
20 weeks
期刊介绍: MicrobiologyOpen is a peer reviewed, fully open access, broad-scope, and interdisciplinary journal delivering rapid decisions and fast publication of microbial science, a field which is undergoing a profound and exciting evolution in this post-genomic era. The journal aims to serve the research community by providing a vehicle for authors wishing to publish quality research in both fundamental and applied microbiology. Our goal is to publish articles that stimulate discussion and debate, as well as add to our knowledge base and further the understanding of microbial interactions and microbial processes. MicrobiologyOpen gives prompt and equal consideration to articles reporting theoretical, experimental, applied, and descriptive work in all aspects of bacteriology, virology, mycology and protistology, including, but not limited to: - agriculture - antimicrobial resistance - astrobiology - biochemistry - biotechnology - cell and molecular biology - clinical microbiology - computational, systems, and synthetic microbiology - environmental science - evolutionary biology, ecology, and systematics - food science and technology - genetics and genomics - geobiology and earth science - host-microbe interactions - infectious diseases - natural products discovery - pharmaceutical and medicinal chemistry - physiology - plant pathology - veterinary microbiology We will consider submissions across unicellular and cell-cluster organisms: prokaryotes (bacteria, archaea) and eukaryotes (fungi, protists, microalgae, lichens), as well as viruses and prions infecting or interacting with microorganisms, plants and animals, including genetic, biochemical, biophysical, bioinformatic and structural analyses. The journal features Original Articles (including full Research articles, Method articles, and Short Communications), Commentaries, Reviews, and Editorials. Original papers must report well-conducted research with conclusions supported by the data presented in the article. We also support confirmatory research and aim to work with authors to meet reviewer expectations. MicrobiologyOpen publishes articles submitted directly to the journal and those referred from other Wiley journals.
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