Department of Human Health & Nutritional Sciences, University of Guelph, Guelph, Ontario, Canada.
Division of Biochemical and Molecular Biology, Friedman School of Nutrition Science and Policy, Tufts University, Boston, Massachusetts, USA.
Ann N Y Acad Sci. 2024 Oct;1540(1):61-88. doi: 10.1111/nyas.15215. Epub 2024 Sep 16.
The gut microbiome may be related to the prevalence of overweight and obesity, but high interindividual variability of the human microbiome complicates our understanding. Obesity often occurs concomitantly with micronutrient deficiencies that impair energy metabolism. Microbiota composition is affected by diet. Host-microbiota interactions are bidirectional. We propose three pathways whereby these interactions may modulate the gut microbiome and obesity: (1) ingested compounds or derivatives affecting small intestinal transit, endogenous secretions, digestion, absorption, microbiome balance, and gut barrier function directly affect host metabolism; (2) substrate availability affecting colonic microbial composition and contact with the gut barrier; and (3) microbial end products affecting host metabolism. The quantity/concentration, duration, and/or frequency (circadian rhythm) of changes in these pathways can alter the gut microbiome, disrupt the gut barrier, alter host immunity, and increase the risk of and progression to overweight and obesity. Host-specific characteristics (e.g., genetic variations) may further affect individual sensitivity and/or resilience to diet- and microbiome-associated perturbations in the colonic environment. In this narrative review, the effects of selected interventions, including fecal microbiota transplantation, dietary calorie restriction, dietary fibers and prebiotics, probiotics and synbiotics, vitamins, minerals, and fatty acids, on the gut microbiome, body weight, and/or adiposity are summarized to help identify mechanisms of action and research opportunities.
肠道微生物组可能与超重和肥胖的流行有关,但人体微生物组的个体间高度可变性使我们对其的理解变得复杂。肥胖通常伴随着影响能量代谢的微量营养素缺乏。微生物组的组成受饮食影响。宿主-微生物组的相互作用是双向的。我们提出了三种可能调节肠道微生物组和肥胖的相互作用途径:(1)摄入的化合物或衍生物直接影响小肠转运、内源性分泌、消化、吸收、微生物组平衡和肠道屏障功能,从而影响宿主代谢;(2)底物可用性影响结肠微生物组成和与肠道屏障的接触;(3)微生物终产物影响宿主代谢。这些途径中的变化的数量/浓度、持续时间和/或频率(昼夜节律)可以改变肠道微生物组,破坏肠道屏障,改变宿主免疫,并增加超重和肥胖的风险和进展。宿主特异性特征(例如遗传变异)可能进一步影响个体对饮食和微生物组相关的结肠环境扰动的敏感性和/或弹性。在这篇叙述性综述中,总结了包括粪便微生物群移植、饮食热量限制、膳食纤维和益生元、益生菌和合生菌、维生素、矿物质和脂肪酸在内的一些干预措施对肠道微生物组、体重和/或肥胖的影响,以帮助确定作用机制和研究机会。