阿尔茨海默病的肠道微生物群:理解分子途径和潜在的治疗前景。

Simone Lista, Antonio Munafò, Filippo Caraci, Camillo Imbimbo, Enzo Emanuele, Piercarlo Minoretti, José Pinto-Fraga, María Merino-País, Paula Crespo-Escobar, Susana López-Ortiz, Giovanni Monteleone, Bruno P Imbimbo, Alejandro Santos-Lozano
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摘要

越来越多的证据表明,肠道微生物群(GM)在阿尔茨海默病(AD)的发病和进展中起着至关重要的作用。这篇叙述性综述探讨了AD中GM、免疫系统和中枢神经系统之间复杂的相互作用。我们讨论了转基因生态失调损害肠道屏障完整性的机制,使促炎分子和代谢物进入体循环和大脑,可能导致AD的特征。此外,我们还研究了转基因可能影响AD风险的其他病理生理机制,包括短链脂肪酸、次级胆油酸和色氨酸代谢物的产生。迷走神经在肠-脑交流中的作用也被讨论。我们强调了靶向转基因治疗AD的潜在治疗意义,重点是抗生素、益生菌、益生元、后益生菌、植物化学物质和粪便微生物群移植。虽然临床前研究显示出希望,但临床证据仍然有限且不一致。我们批判性地评估临床试验,强调将转基因疗法转化为AD患者所面临的挑战。综述的证据强调需要进一步研究阐明转基因与AD之间的精确分子机制,并确定转基因生态失调是AD病理的促成因素还是后果。未来的研究应侧重于大规模的临床试验,以验证基于转基因的干预措施对AD的有效性和安全性。
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Gut microbiota in Alzheimer's disease: Understanding molecular pathways and potential therapeutic perspectives.

Accumulating evidence suggests that gut microbiota (GM) plays a crucial role in Alzheimer's disease (AD) pathogenesis and progression. This narrative review explores the complex interplay between GM, the immune system, and the central nervous system in AD. We discuss mechanisms through which GM dysbiosis can compromise intestinal barrier integrity, enabling pro-inflammatory molecules and metabolites to enter systemic circulation and the brain, potentially contributing to AD hallmarks. Additionally, we examine other pathophysiological mechanisms by which GM may influence AD risk, including the production of short-chain fatty acids, secondary bile acids, and tryptophan metabolites. The role of the vagus nerve in gut-brain communication is also addressed. We highlight potential therapeutic implications of targeting GM in AD, focusing on antibiotics, probiotics, prebiotics, postbiotics, phytochemicals, and fecal microbiota transplantation. While preclinical studies showed promise, clinical evidence remains limited and inconsistent. We critically assess clinical trials, emphasizing challenges in translating GM-based therapies to AD patients. The reviewed evidence underscores the need for further research to elucidate precise molecular mechanisms linking GM to AD and determine whether GM dysbiosis is a contributing factor or consequence of AD pathology. Future studies should focus on large-scale clinical trials to validate GM-based interventions' efficacy and safety in AD.

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