Bidirectional crosstalk between the gut microbiota and cellular compartments of brain: Implications for neurodevelopmental and neuropsychiatric disorders.

IF 6.2 1区 医学 Q1 PSYCHIATRY
Seyedeh Marziyeh Jabbari Shiadeh, Wing Ki Chan, Sofia Rasmusson, Noor Hassan, Sâmia Joca, Lars Westberg, Anders Elfvin, Carina Mallard, Maryam Ardalan
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Abstract

The gut-brain axis serves as a crucial communication pathway, with microbial metabolites such as short-chain fatty acids (SCFAs) playing a central role in regulating neuroinflammation and maintaining neuronal health. The gut microbiota's impact on neurodevelopment is highlighted, particularly its relevance to autism, anxiety, and other psychiatric conditions. In this review, we explored the intricate relationship between the gut microbiota (GM) and the central nervous system (CNS), emphasizing the bidirectional communication that forms the gut-brain axis. Associations between specific gut microbiota and neurodegenerative diseases are explored, focusing on the role of certain bacteria in processes such as amyloid aggregation and neuroinflammation in Alzheimer's disease (AD) and Parkinson's disease (PD). The potential for therapeutic modulation of the gut microbiota is discussed, with a focus on dietary interventions and probiotics as strategies to improve outcomes in neurodegenerative diseases by restoring gut health. We concluded by emphasizing the significance of understanding the gut-brain connection and calls for further research to investigate therapeutic approaches targeting the gut microbiome for brain health.

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肠道微生物群和大脑细胞间的双向串扰:对神经发育和神经精神疾病的影响。
肠-脑轴是一个重要的通讯途径,微生物代谢物如短链脂肪酸(SCFAs)在调节神经炎症和维持神经元健康方面发挥着核心作用。肠道微生物群对神经发育的影响被强调,特别是它与自闭症、焦虑和其他精神疾病的相关性。在这篇综述中,我们探讨了肠道微生物群(GM)和中枢神经系统(CNS)之间的复杂关系,强调了形成肠-脑轴的双向交流。探讨特定肠道微生物群与神经退行性疾病之间的关联,重点关注某些细菌在阿尔茨海默病(AD)和帕金森病(PD)中淀粉样蛋白聚集和神经炎症等过程中的作用。讨论了肠道微生物群治疗调节的潜力,重点是饮食干预和益生菌作为通过恢复肠道健康来改善神经退行性疾病结局的策略。最后,我们强调了理解肠-脑连接的重要性,并呼吁进一步研究针对肠道微生物群的脑健康治疗方法。
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来源期刊
CiteScore
11.50
自引率
2.90%
发文量
484
审稿时长
23 weeks
期刊介绍: Psychiatry has suffered tremendously by the limited translational pipeline. Nobel laureate Julius Axelrod''s discovery in 1961 of monoamine reuptake by pre-synaptic neurons still forms the basis of contemporary antidepressant treatment. There is a grievous gap between the explosion of knowledge in neuroscience and conceptually novel treatments for our patients. Translational Psychiatry bridges this gap by fostering and highlighting the pathway from discovery to clinical applications, healthcare and global health. We view translation broadly as the full spectrum of work that marks the pathway from discovery to global health, inclusive. The steps of translation that are within the scope of Translational Psychiatry include (i) fundamental discovery, (ii) bench to bedside, (iii) bedside to clinical applications (clinical trials), (iv) translation to policy and health care guidelines, (v) assessment of health policy and usage, and (vi) global health. All areas of medical research, including — but not restricted to — molecular biology, genetics, pharmacology, imaging and epidemiology are welcome as they contribute to enhance the field of translational psychiatry.
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