["Pseudoneurotransmission" and gut microbiome - brain communication in neuropsychiatric disorders].

Q3 Medicine
Christos Ch Liapis
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引用次数: 0

Abstract

The gut microbiome, which comprises symbiotic bacteria colonizing the human digestive tract, undergoes dynamic changes during the lifespan, as evidenced by the fact that the number of species and the diversity of their composition decrease significantly with age. The aim of this review is to illuminate bilateral neuroimmunological pathways that determine the role of gut microbiome dysbiosis, not only as a cause but also as a byproduct of many neurodegenerative diseases of the CNS, such as Alzheimer's disease (AD) and Parkinson's disease (PD), but also in the frame of several behavioral and psychiatric pathological conditions such as depressive and anxiety disorders, schizophrenia, and autism spectrum disorder (ASD). Dysbiosis, in particular, reveals a model of "deceptive" mimicry of host molecules that might cause abnormal folding ("misfolding") and pathological aggregation of Aβ-peptide, leading to its dispersion through the gut-brain axis, precipitating microglia cell activation. By controlling myelination at the prefrontal cortex (PFC), a crucial area for multifaceted cognitive behavior, forecasting, and decision-making, the gut/microbiome-brain axis influences mood and social behavior, since major depressive disorder is correlated to white matter disturbance in the PFC, due to disregulations in the expression of myelin-related mRNA in this area. The gut microbiome is altered in psychosis compared to healthy controls, while medication with antipsychotics may result in reduced microbial community diversity. The vagus nerve, as a key element of the parasympathetic nervous system, regulating immune responses, may "detect" gut microbiome metabolites and transfer this intestinal information to the CNS, through its afferents, as in a "pseudo-neurotransmission" process. Scientific interest towards microbiome-based therapies increases as psychobiotics (which are strains of probiotics/prebiotics with specific properties to influence the gut-brain axis) appear to be able to exercise a beneficial effect in many CNS disorders. Lifestyle modifications, such as dietary interventions via psychobiotics intake that might enhance the gut microbiome's ability to produce beneficial metabolites that exert therapeutic effects on intestinal permeability, cognitive function, and immunity, may reveal new research pathways and therapeutic directions leading to a radical change of the "epistemology paradigm" as far as prevention and treatment of major neuro-psychiatric disorders is concerned.

[神经精神疾病中的 "假神经传导 "和肠道微生物组-大脑交流]。
肠道菌群是由寄生在人体消化道的共生细菌组成的,在人的一生中会发生动态变化,其物种数量和组成多样性随着年龄的增长而显著减少。本综述的目的是阐明决定肠道微生物群失调作用的双侧神经免疫途径,肠道微生物群失调不仅是许多中枢神经退行性疾病(如阿尔茨海默病(AD)和帕金森病(PD))的原因,也是副产物,而且在一些行为和精神病理状况(如抑郁症和焦虑症,精神分裂症和自闭症谱系障碍(ASD))的框架内。特别是,生态失调揭示了宿主分子的“欺骗性”模仿模型,该模型可能导致a β-肽的异常折叠(“错误折叠”)和病理聚集,导致其通过肠-脑轴分散,促进小胶质细胞活化。通过控制前额叶皮层(PFC)的髓鞘形成,肠道/微生物组-脑轴影响情绪和社会行为,因为重度抑郁症与PFC的白质紊乱相关,这是由于该区域髓鞘相关mRNA表达失调。PFC是多方面认知行为、预测和决策的关键区域。与健康对照相比,精神病患者的肠道微生物群发生了改变,而抗精神病药物可能导致微生物群落多样性降低。迷走神经作为副交感神经系统的关键组成部分,调节免疫反应,可以“检测”肠道微生物代谢物,并通过传入神经将肠道信息传递给中枢神经系统,就像“伪神经传递”过程一样。随着精神益生菌(具有影响肠-脑轴的特定特性的益生菌/益生元菌株)似乎能够在许多中枢神经系统疾病中发挥有益作用,对基于微生物组的治疗的科学兴趣也在增加。生活方式的改变,如通过摄入心理生物制剂进行饮食干预,可能会增强肠道微生物群产生有益代谢物的能力,从而对肠道通透性、认知功能和免疫力产生治疗作用,这可能会揭示新的研究途径和治疗方向,从而彻底改变“认识论范式”,就主要神经精神疾病的预防和治疗而言。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Psychiatrike = Psychiatriki
Psychiatrike = Psychiatriki Medicine-Medicine (all)
CiteScore
2.60
自引率
0.00%
发文量
37
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