R Pavithra, N V Kanimozhi, L Sonali, Chinta Suneetha, M Sukumar
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Furthermore, Toll-like receptor 4 -4-mediated microglial responses are triggered by Gram-negative bacterial lipopolysaccharides. This cascade promotes oxidative stress, chronic neuroinflammation, and disruption of the (BBB) blood-brain barrier, all of which encourage the accumulation of neurotoxic proteins. Microbiome-modulating therapies, such as probiotics, prebiotics, and synbiotics, have been shown to have neuroprotective properties. They work by restoring microbial diversity, increasing (Short-chain fatty acids) SCFA-mediated anti-inflammatory pathways, and reducing glial activation. In addition to promoting gut microbiota equilibrium, dietary approaches like the Mediterranean and ketogenic diets, which are enhanced with polyphenols and omega-3 fatty acids, also lower systemic inflammation and increase neural resilience. Furthermore, the potential of postbiotics and fecal microbiota transplantation to attenuate AD-related neurodegeneration and restore gut-derived metabolic balance is being investigated. Translating these methods into standardized clinical applications is difficult, though, because individual microbiome composition varies. 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引用次数: 0
摘要
阿尔茨海默病(AD)是一种神经退行性疾病,其特征是神经炎症、tau蛋白过度磷酸化、a β (β淀粉样蛋白)积累和突触功能障碍。新的研究表明,肠-脑轴是一个双向通信网络,涉及免疫信号、神经通路和微生物代谢物,使得肠道微生物群的生态失调对阿尔茨海默病的发病至关重要。肠道菌群组成的改变会阻碍关键代谢物的产生,如短链脂肪酸、三甲胺- n -氧化物和次级胆汁酸,这些代谢物会影响神经炎症级联反应、线粒体生物能量学和突触可塑性。此外,toll样受体4- 4介导的小胶质细胞反应是由革兰氏阴性细菌脂多糖引发的。这种级联反应会促进氧化应激、慢性神经炎症和血脑屏障的破坏,所有这些都会促进神经毒性蛋白的积累。微生物组调节疗法,如益生菌、益生元和合成菌,已被证明具有神经保护特性。它们通过恢复微生物多样性、增加(短链脂肪酸)scfa介导的抗炎途径和减少胶质细胞激活来起作用。除了促进肠道菌群平衡外,地中海饮食和生酮饮食等饮食方法(多酚和omega-3脂肪酸增强)还能降低全身炎症,增强神经弹性。此外,正在研究后生物制剂和粪便微生物群移植在减轻ad相关神经退行性变和恢复肠道源性代谢平衡方面的潜力。然而,将这些方法转化为标准化的临床应用是困难的,因为个体微生物组的组成各不相同。通过机制研究和广泛的临床试验来解决这些并发症将是至关重要的,以建立肠道微生物群作为阿尔茨海默病有希望的治疗靶点。
Unveiling Role of Gut Microbiota in Alzheimer's Disease: Mechanisms, Challenges and Future Perspectives.
Alzheimer's disease (AD) is a neurodegenerative condition characterized by neuroinflammation, tau hyperphosphorylation, Aβ (Amyloid beta) accumulation, and synaptic dysfunction. New research indicates that the gut-brain axis, a network of two-way communication that involves immunological signals, neural pathways, and microbial metabolites, makes dysbiosis of the gut microbiota essential to the pathogenesis of AD. Alterations in the gut microbiota's composition hinder the production of crucial metabolites, such as short-chain fatty acids, trimethylamine- N-oxide, and secondary bile acids, which affect neuroinflammatory cascades, mitochondrial bioenergetics, and synaptic plasticity. Furthermore, Toll-like receptor 4 -4-mediated microglial responses are triggered by Gram-negative bacterial lipopolysaccharides. This cascade promotes oxidative stress, chronic neuroinflammation, and disruption of the (BBB) blood-brain barrier, all of which encourage the accumulation of neurotoxic proteins. Microbiome-modulating therapies, such as probiotics, prebiotics, and synbiotics, have been shown to have neuroprotective properties. They work by restoring microbial diversity, increasing (Short-chain fatty acids) SCFA-mediated anti-inflammatory pathways, and reducing glial activation. In addition to promoting gut microbiota equilibrium, dietary approaches like the Mediterranean and ketogenic diets, which are enhanced with polyphenols and omega-3 fatty acids, also lower systemic inflammation and increase neural resilience. Furthermore, the potential of postbiotics and fecal microbiota transplantation to attenuate AD-related neurodegeneration and restore gut-derived metabolic balance is being investigated. Translating these methods into standardized clinical applications is difficult, though, because individual microbiome composition varies. It will be essential to address these complications through mechanistic research and extensive clinical trials to establish gut microbiota as a promising therapeutic target in AD.