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实验饮食决定了益生菌在肥胖中的代谢益处。

Experimental diets dictate the metabolic benefits of probiotics in obesity.

机构信息

Quebec Heart and Lung Institute, Faculty of Medicine, and Institute of Nutrition and Functional Foods (INAF), Laval University, Quebec, QC, Canada.

Institute of Nutritional Medicine, University of Lübeck, Lübeck, Germany.

出版信息

Gut Microbes. 2023 Jan-Dec;15(1):2192547. doi: 10.1080/19490976.2023.2192547.

Abstract

Growing evidence supports the use of probiotics to prevent or mitigate obesity-related dysmetabolism and non-alcoholic fatty liver disease (NAFLD). However, frequent reports of responders versus non-responders to probiotic treatment warrant a better understanding of key modifiers of host-microbe interactions. The influence of host diet on probiotic efficacy, in particular against metabolic diseases, remains elusive. We fed C57BL6/J mice a low fat reference diet or one of two energy-matched high fat and high sucrose diets for 12 weeks; a classical high fat diet (HFD) and a customized fast food-mimicking diet (FFMD). During the studies, mice fed either obesogenic diet were gavaged daily with one of two probiotic lactic acid bacteria (LAB) strains previously classified as , namely ()or subsp. (), or vehicle. The tested probiotics exhibited a reproducible efficacy but dichotomous response according to the obesogenic diets used. Indeed, prevented weight gain, improved insulin sensitivity, and protected against NAFLD development in mice fed HFD, but not FFMD. Conversely, improved glucoregulatory capacity, reduced NAFLD development, and increased distal gut bile acid levels associated with changes in predicted functions of the gut microbiota exclusively in the context of FFMD-feeding. We found that the probiotic efficacy of two LAB strains is highly dependent on experimental obesogenic diets. These findings highlight the need to carefully consider the confounding impact of diet in order to improve both the reproducibility of preclinical probiotic studies and their clinical research translatability.

摘要

越来越多的证据支持使用益生菌来预防或减轻与肥胖相关的代谢紊乱和非酒精性脂肪性肝病(NAFLD)。然而,益生菌治疗的应答者与无应答者的频繁报告需要更好地了解宿主-微生物相互作用的关键修饰因子。宿主饮食对益生菌疗效的影响,特别是针对代谢疾病的影响,仍然难以捉摸。我们用低脂参考饮食或两种能量匹配的高脂肪和高蔗糖饮食喂养 C57BL6/J 小鼠 12 周;一种是经典的高脂肪饮食(HFD),另一种是定制的快餐模拟饮食(FFMD)。在研究期间,喂食肥胖饮食的小鼠每天用两种已分类为益生菌乳酸菌(LAB)菌株中的一种进行灌胃,分别为 ()或亚种。()或亚种。(),或载体。经过测试的益生菌表现出可重复的疗效,但根据使用的肥胖诱导饮食表现出二分法反应。事实上,预防了 HFD 喂养小鼠的体重增加、改善了胰岛素敏感性,并防止了 NAFLD 的发展,但对 FFMD 没有作用。相反,在 FFMD 喂养的情况下,改善了葡萄糖调节能力、减少了 NAFLD 的发展,并增加了与肠道微生物群预测功能变化相关的远端肠道胆汁酸水平,但只在 FFMD 喂养的情况下。我们发现,两种 LAB 菌株的益生菌疗效高度依赖于实验性肥胖诱导饮食。这些发现强调了需要仔细考虑饮食的混杂影响,以提高临床前益生菌研究的重现性及其临床研究的可转化性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/782b/10038044/d21850816d94/KGMI_A_2192547_UF0001_OC.jpg

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