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维生素A、膳食纤维与微生物群-肠-脑轴之间的协同相互作用:预防阿尔茨海默病的潜在机制。

The synergistic interplay between vitamin A, dietary fiber, and the microbiota-gut-brain axis: a potential mechanism for preventing Alzheimer's disease.

作者信息

Skawratananond Shadt, McCrea Grace E, Lie Paul, Buxton Matthew B, Daly Sean P, Vojtkofsky Nicholas A, Smith Shane C, Zhang Charlie, Hernandez Matthew, Hindle Ashly, Logsdon Aric F, Lawrence J Josh

机构信息

Department of Pharmacology and Neuroscience, Texas Tech University Health Sciences Center, Lubbock, Texas, United States.

School of Medicine, Texas Tech University Health Sciences Center, Lubbock, Texas, United States.

出版信息

Am J Physiol Gastrointest Liver Physiol. 2025 Sep 1;329(3):G484-G499. doi: 10.1152/ajpgi.00097.2025. Epub 2025 Aug 12.

Abstract

The human gastrointestinal tract harbors a vast and diverse microbial community, with the gut microbiome playing a fundamental role in numerous biological processes that influence overall health and disease progression. Emerging evidence has identified bacterial lipopolysaccharides in the hippocampus of patients with Alzheimer's disease (AD), highlighting the intricate relationship between the gastrointestinal tract, gut microbiome, and the central and enteric nervous systems-commonly referred to as the "microbiota-gut-brain axis." In this review, we explore the mechanisms by which the microbiota-gut-brain axis contributes to AD pathogenesis. We propose that sufficient levels of all-trans retinoic acid (ATRA), the bioactive form of vitamin A, enhance intestinal barrier integrity by upregulating tight junction proteins and modulating immune function through the induction of regulatory T-cell differentiation, thereby mitigating inflammation. Furthermore, dietary fiber complements this process by promoting the production of short-chain fatty acids, such as butyrate, via bacterial fermentation. Butyrate, in turn, acts as a histone deacetylase inhibitor, upregulating ATRA bioavailability by elevating aldehyde dehydrogenase gene expression. Our mechanistic framework is supported by the endotoxin hypothesis of AD, which maintains that the movement of infectious pathogens across the blood-brain barrier causes a vicious cycle of inflammation, a key factor of AD pathogenesis, leading to amyloid-β deposition, microglial activation, and CYP26A1-mediated ATRA degradation. Finally, we discuss microbiome-based therapeutic strategies and dietary interventions, including prebiotic compounds, probiotic bacteria, fecal microbiota transplantation, the Mediterranean-DASH Intervention for Neurodegenerative Delay (MIND) diet, and a combined approach featuring vitamins A/D and dietary fiber, as potential approaches to prevent progression to AD via the microbiota-gut-brain axis.

摘要

人类胃肠道中栖息着庞大而多样的微生物群落,肠道微生物群在影响整体健康和疾病进展的众多生物过程中发挥着重要作用。新出现的证据已在阿尔茨海默病(AD)患者的海马体中发现了细菌脂多糖,这凸显了胃肠道、肠道微生物群与中枢和肠神经系统之间的复杂关系,这种关系通常被称为“微生物群-肠-脑轴”。在本综述中,我们探讨了微生物群-肠-脑轴促成AD发病机制的方式。我们提出,全反式维甲酸(ATRA)(维生素A的生物活性形式)的充足水平通过上调紧密连接蛋白来增强肠道屏障完整性,并通过诱导调节性T细胞分化来调节免疫功能,从而减轻炎症。此外,膳食纤维通过细菌发酵促进短链脂肪酸(如丁酸)的产生来补充这一过程。反过来,丁酸作为一种组蛋白脱乙酰酶抑制剂,通过提高醛脱氢酶基因表达来上调ATRA的生物利用度。我们的机制框架得到了AD内毒素假说的支持,该假说认为感染性病原体穿过血脑屏障会导致炎症的恶性循环,这是AD发病机制的一个关键因素,导致淀粉样β蛋白沉积、小胶质细胞激活和CYP26A1介导的ATRA降解。最后,我们讨论了基于微生物群的治疗策略和饮食干预措施,包括益生元化合物、益生菌、粪便微生物群移植、地中海-得舒饮食延缓神经退行性变干预(MIND)饮食,以及以维生素A/D和膳食纤维为特色的联合方法,作为通过微生物群-肠-脑轴预防进展为AD的潜在方法。

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