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肠道微生物群代谢产物:阿尔茨海默病的潜在治疗靶点?

Gut microbiota metabolites: potential therapeutic targets for Alzheimer's disease?

作者信息

Zhang Shanshan, Lu Jing, Jin Ziqi, Xu Hanying, Zhang Dongmei, Chen Jianan, Wang Jian

机构信息

The School to Changchun University of Chinese Medicine, Changchun, China.

Research Center of Traditional Chinese Medicine, The Affiliated Hospital to Changchun University of Chinese Medicine, Changchun, China.

出版信息

Front Pharmacol. 2024 Sep 17;15:1459655. doi: 10.3389/fphar.2024.1459655. eCollection 2024.

Abstract

BACKGROUND

Alzheimer's disease (AD) is a neurodegenerative disease characterized by progressive decline in cognitive function, which significantly increases pain and social burden. However, few therapeutic interventions are effective in preventing or mitigating the progression of AD. An increasing number of recent studies support the hypothesis that the gut microbiome and its metabolites may be associated with upstream regulators of AD pathology.

METHODS

In this review, we comprehensively explore the potential mechanisms and currently available interventions targeting the microbiome for the improvement of AD. Our discussion is structured around modern research advancements in AD, the bidirectional communication between the gut and brain, the multi-target regulatory effects of microbial metabolites on AD, and therapeutic strategies aimed at modulating gut microbiota to manage AD.

RESULTS

The gut microbiota plays a crucial role in the pathogenesis of AD through continuous bidirectional communication via the microbiota-gut-brain axis. Among these, microbial metabolites such as lipids, amino acids, bile acids and neurotransmitters, especially sphingolipids and phospholipids, may serve as central components of the gut-brain axis, regulating AD-related pathogenic mechanisms including β-amyloid metabolism, Tau protein phosphorylation, and neuroinflammation. Additionally, interventions such as probiotic administration, fecal microbiota transplantation, and antibiotic use have also provided evidence supporting the association between gut microbiota and AD. At the same time, we propose an innovative strategy for treating AD: a healthy lifestyle combined with targeted probiotics and other potential therapeutic interventions, aiming to restore intestinal ecology and microbiota balance.

CONCLUSION

Despite previous efforts, the molecular mechanisms by which gut microbes act on AD have yet to be fully described. However, intestinal microorganisms may become an essential target for connecting the gut-brain axis and improving the symptoms of AD. At the same time, it requires joint exploration by multiple centers and multiple disciplines.

摘要

背景

阿尔茨海默病(AD)是一种神经退行性疾病,其特征为认知功能进行性衰退,这显著增加了痛苦和社会负担。然而,很少有治疗干预措施能有效预防或减轻AD的进展。最近越来越多的研究支持这样一种假说,即肠道微生物群及其代谢产物可能与AD病理的上游调节因子有关。

方法

在本综述中,我们全面探讨了针对微生物群改善AD的潜在机制和目前可用的干预措施。我们围绕AD的现代研究进展、肠道与大脑之间的双向通信、微生物代谢产物对AD的多靶点调节作用以及旨在调节肠道微生物群以管理AD的治疗策略展开讨论。

结果

肠道微生物群通过微生物-肠道-脑轴的持续双向通信在AD的发病机制中起关键作用。其中,脂质、氨基酸、胆汁酸和神经递质等微生物代谢产物,尤其是鞘脂和磷脂,可能作为肠-脑轴的核心成分,调节与AD相关的致病机制,包括β-淀粉样蛋白代谢、Tau蛋白磷酸化和神经炎症。此外,益生菌给药、粪便微生物群移植和抗生素使用等干预措施也提供了支持肠道微生物群与AD之间关联的证据。同时,我们提出了一种治疗AD的创新策略:健康的生活方式结合靶向益生菌和其他潜在的治疗干预措施,旨在恢复肠道生态和微生物群平衡。

结论

尽管此前已做出努力,但肠道微生物作用于AD的分子机制尚未完全阐明。然而,肠道微生物可能成为连接肠-脑轴和改善AD症状的重要靶点。同时,这需要多个中心和多学科的联合探索。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/773d/11442227/1bc2f36413b8/fphar-15-1459655-g001.jpg

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