果糖分解代谢及其代谢效应:探索宿主-微生物群相互作用和种族的影响。

IF 4.7 2区 医学 Q1 NEUROSCIENCES
Florine H M Westerbeke, Melany Rios-Morales, Ilias Attaye, Max Nieuwdorp
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引用次数: 0

摘要

在肥胖症和相关非传染性疾病(NCDs)(包括 2 型糖尿病(T2D)和代谢功能障碍相关性脂肪肝(MASLD))的患病率方面,不同种族群体之间存在着严重的健康差异。然而,人们对造成这些差异的潜在因素仍然知之甚少。果糖被广泛认为是这些非传染性疾病的潜在介质,因为肝脏果糖分解可导致有害的代谢效应,包括胰岛素抵抗和肝脏脂肪变性。此外,肠道微生物群对果糖的发酵可产生乙醇和乙酸盐等代谢物,这两种物质都是新生脂肪生成(DNL)的潜在底物,因此可能会导致这些代谢疾病的发生。据观察,不同种族之间的肠道微生物群组成存在显著差异。此外,不同种族群体的果糖摄入量也不尽相同,果糖摄入量已被证实会显著改变肠道微生物群的组成,从而影响其发酵特性和代谢作用。因此,肠道微生物群组成的种族差异可能会受到果糖摄入量变化的影响,从而导致观察到的健康差异。本综述概述了宿主与微生物果糖分解之间复杂的相互作用、种族在塑造这些代谢过程中的作用及其对宿主健康的影响。了解这些相互作用有助于深入了解造成种族健康差异的机制,从而改进个性化营养策略。要点:近几十年来,膳食中果糖的摄入量大幅增加,这与肥胖症和非传染性疾病(NCD)(如 2 型糖尿病和代谢功能障碍相关性脂肪肝)发病率的上升有关。不同种族群体在非传染性疾病发病率和膳食果糖消耗量方面存在明显差异,这凸显了阐明果糖分解代谢及其健康影响的内在机制的必要性。除了众所周知的肝脏果糖分解代谢的毒性作用外,新出现的证据还强调了小肠微生物群在将果糖等糖类发酵成具有潜在有害代谢影响的各种细菌产物中的作用。肠道微生物群的组成存在着明显的种族差异,再加上果糖摄入量的不同,可能会导致观察到的健康差异。为了全面了解肠道微生物群在介导果糖诱导的不良代谢效应中的作用,未来的研究应侧重于小肠微生物群。未来有关果糖-微生物群-宿主相互作用的研究应考虑饮食习惯和微生物组成的种族差异,以阐明肠道微生物群在推动上述健康差异方面的潜在作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Fructose catabolism and its metabolic effects: Exploring host-microbiota interactions and the impact of ethnicity.

Important health disparities are observed in the prevalence of obesity and associated non-communicable diseases (NCDs), including type 2 diabetes (T2D) and metabolic dysfunction-associated steatotic liver disease (MASLD) among ethnic groups. Yet, the underlying factors accounting for these disparities remain poorly understood. Fructose has been widely proposed as a potential mediator of these NCDs, given that hepatic fructose catabolism can result in deleterious metabolic effects, including insulin resistance and hepatic steatosis. Moreover, the fermentation of fructose by the gut microbiota can produce metabolites such as ethanol and acetate, both which serve as potential substrates for de novo lipogenesis (DNL) and could therefore contribute to the development of these metabolic conditions. Significant inter-ethnic differences in gut microbiota composition have been observed. Moreover, fructose consumption varies across ethnic groups, and fructose intake has been demonstrated to significantly alter gut microbiota composition, which can influence its fermenting properties and metabolic effects. Therefore, ethnic differences in gut microbiota composition, which may be influenced by variations in fructose consumption, could contribute to the observed health disparities. This review provides an overview of the complex interactions between host and microbial fructose catabolism, the role of ethnicity in shaping these metabolic processes and their impact on host health. Understanding these interactions could provide insights into the mechanisms driving ethnic health disparities to improve personalized nutrition strategies. KEY POINTS: Dietary fructose consumption has increased substantially over recent decades, which has been associated with the rising prevalence of obesity and non-communicable diseases (NCDs) such as type 2 diabetes and metabolic dysfunction-associated steatotic liver disease. Pronounced disparities among different ethnic groups in NCD prevalence and dietary fructose consumption underscore the need to elucidate the underlying mechanisms of fructose catabolism and its health effects. Together with the well-known toxic effects of hepatic fructose catabolism, emerging evidence highlights a role for the small intestinal microbiota in fermenting sugars like fructose into various bacterial products with potential deleterious metabolic effects. There are significant ethnic differences in gut microbiota composition that, combined with varying fructose consumption, could mediate the observed health disparities. To comprehensively understand the role of the gut microbiota in mediating fructose-induced adverse metabolic effects, future research should focus on the small intestinal microbiota. Future research on fructose - microbiota - host interactions should account for ethnic differences in dietary habits and microbial composition to elucidate the potential role of the gut microbiota in driving the mentioned health disparities.

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来源期刊
Journal of Physiology-London
Journal of Physiology-London 医学-神经科学
CiteScore
9.70
自引率
7.30%
发文量
817
审稿时长
2 months
期刊介绍: The Journal of Physiology publishes full-length original Research Papers and Techniques for Physiology, which are short papers aimed at disseminating new techniques for physiological research. Articles solicited by the Editorial Board include Perspectives, Symposium Reports and Topical Reviews, which highlight areas of special physiological interest. CrossTalk articles are short editorial-style invited articles framing a debate between experts in the field on controversial topics. Letters to the Editor and Journal Club articles are also published. All categories of papers are subjected to peer reivew. The Journal of Physiology welcomes submitted research papers in all areas of physiology. Authors should present original work that illustrates new physiological principles or mechanisms. Papers on work at the molecular level, at the level of the cell membrane, single cells, tissues or organs and on systems physiology are all acceptable. Theoretical papers and papers that use computational models to further our understanding of physiological processes will be considered if based on experimentally derived data and if the hypothesis advanced is directly amenable to experimental testing. While emphasis is on human and mammalian physiology, work on lower vertebrate or invertebrate preparations may be suitable if it furthers the understanding of the functioning of other organisms including mammals.
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