High-fat diet, intestinal microecology and bone loss.

IF 4.1 2区 医学 Q2 NUTRITION & DIETETICS
Ning Wang, Xue Tong, Yi-Kai Li
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引用次数: 0

Abstract

Bone, a vital component of the human body, plays a crucial role in maintaining mobility and systemic health. Growing evidence underscores the complex interplay between a high-fat diet (HFD), intestinal microecology, and bone loss. This review consolidates findings across three interconnected mechanisms: (1) HFD compromises bone homeostasis by reducing bone mineral density (BMD) and disrupting microarchitecture, driven by bone marrow adiposity, oxidative stress, and chronic inflammation; (2) HFD disrupts intestinal microecology through microbiota dysbiosis (e.g., elevated Firmicutes/Bacteroidetes ratio, depletion of Bifidobacterium), epithelial barrier impairment (e.g., suppressed Mucin2 secretion, downregulated tight junction proteins), and immune dysregulation (e.g., Th17/Treg imbalance, diminished IL-10 production); and (3) intestinal microecology imbalances exacerbate bone loss through microbial metabolite alterations (e.g., a deficiency of short-chain fatty acids impairing Treg-mediated Wnt10b signaling), systemic inflammation from barrier leakage, and intestinal immune cell trafficking (e.g., Th17 migration to bone marrow). These interconnected mechanisms point to an indirect pathway by which HFD contributes to bone loss through alterations in intestinal microecology. While this indirect relationship remains insufficiently validated, accumulating evidence highlights the important roles of HFD and intestinal microecology in bone regulation. This review aims to comprehensively examine the connections between HFD, intestinal microecology, and bone loss, with a focus on elucidating these potential mechanisms. Given diet's profound impact on intestinal microecology, optimizing dietary patterns to rebalance intestinal microecology offers a promising strategy for preventing and treating bone-related disorders.

高脂肪饮食、肠道微生态和骨质流失。
骨骼是人体的重要组成部分,在维持活动能力和全身健康方面起着至关重要的作用。越来越多的证据强调了高脂肪饮食(HFD)、肠道微生态和骨质流失之间复杂的相互作用。这篇综述整合了三个相互关联的机制的发现:(1)HFD通过降低骨密度(BMD)和破坏微结构来破坏骨稳态,由骨髓肥胖、氧化应激和慢性炎症驱动;(2) HFD通过微生物群失调(如厚壁菌门/拟杆菌门比例升高、双歧杆菌减少)、上皮屏障损伤(如抑制Mucin2分泌、下调紧密连接蛋白)和免疫失调(如Th17/Treg失衡、IL-10产生减少)破坏肠道微生态;(3)肠道微生态失衡通过微生物代谢物的改变(例如,短链脂肪酸的缺乏损害treg介导的Wnt10b信号)、屏障渗漏引起的全身性炎症和肠道免疫细胞运输(例如Th17迁移到骨髓)加剧骨质流失。这些相互关联的机制指出了HFD通过改变肠道微生态导致骨质流失的间接途径。虽然这种间接关系尚未得到充分验证,但越来越多的证据表明HFD和肠道微生态在骨骼调节中的重要作用。本文旨在全面探讨HFD、肠道微生态和骨质流失之间的联系,并重点阐明这些潜在的机制。鉴于饮食对肠道微生态的深远影响,优化饮食模式以重新平衡肠道微生态为预防和治疗骨相关疾病提供了一种有希望的策略。
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来源期刊
Nutrition & Metabolism
Nutrition & Metabolism 医学-营养学
CiteScore
8.40
自引率
0.00%
发文量
78
审稿时长
4-8 weeks
期刊介绍: Nutrition & Metabolism publishes studies with a clear focus on nutrition and metabolism with applications ranging from nutrition needs, exercise physiology, clinical and population studies, as well as the underlying mechanisms in these aspects. The areas of interest for Nutrition & Metabolism encompass studies in molecular nutrition in the context of obesity, diabetes, lipedemias, metabolic syndrome and exercise physiology. Manuscripts related to molecular, cellular and human metabolism, nutrient sensing and nutrient–gene interactions are also in interest, as are submissions that have employed new and innovative strategies like metabolomics/lipidomics or other omic-based biomarkers to predict nutritional status and metabolic diseases. Key areas we wish to encourage submissions from include: -how diet and specific nutrients interact with genes, proteins or metabolites to influence metabolic phenotypes and disease outcomes; -the role of epigenetic factors and the microbiome in the pathogenesis of metabolic diseases and their influence on metabolic responses to diet and food components; -how diet and other environmental factors affect epigenetics and microbiota; the extent to which genetic and nongenetic factors modify personal metabolic responses to diet and food compositions and the mechanisms involved; -how specific biologic networks and nutrient sensing mechanisms attribute to metabolic variability.
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