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社交焦虑障碍相关的肠道微生物群会增加社交恐惧。

Social anxiety disorder-associated gut microbiota increases social fear.

机构信息

Alimentary Pharmabiotic Centre Microbiome Ireland, University College Cork, Cork T12YT20, Ireland.

Department of Anatomy and Neuroscience, University College Cork, Cork T12YT20, Ireland.

出版信息

Proc Natl Acad Sci U S A. 2024 Jan 2;121(1):e2308706120. doi: 10.1073/pnas.2308706120. Epub 2023 Dec 26.

Abstract

Social anxiety disorder (SAD) is a crippling psychiatric disorder characterized by intense fear or anxiety in social situations and their avoidance. However, the underlying biology of SAD is unclear and better treatments are needed. Recently, the gut microbiota has emerged as a key regulator of both brain and behaviour, especially those related to social function. Moreover, increasing data supports a role for immune function and oxytocin signalling in social responses. To investigate whether the gut microbiota plays a causal role in modulating behaviours relevant to SAD, we transplanted the microbiota from SAD patients, which was identified by 16S rRNA sequencing to be of a differential composition compared to healthy controls, to mice. Although the mice that received the SAD microbiota had normal behaviours across a battery of tests designed to assess depression and general anxiety-like behaviours, they had a specific heightened sensitivity to social fear, a model of SAD. This distinct heightened social fear response was coupled with changes in central and peripheral immune function and oxytocin expression in the bed nucleus of the stria terminalis. This work demonstrates an interkingdom basis for social fear responses and posits the microbiome as a potential therapeutic target for SAD.

摘要

社交焦虑障碍(SAD)是一种使人衰弱的精神疾病,其特征是在社交场合中产生强烈的恐惧或焦虑,并回避这些场合。然而,SAD 的潜在生物学机制尚不清楚,需要更好的治疗方法。最近,肠道微生物群已成为大脑和行为的关键调节剂,特别是与社交功能相关的大脑和行为。此外,越来越多的数据支持免疫功能和催产素信号在社交反应中的作用。为了研究肠道微生物群是否在调节与 SAD 相关的行为方面发挥因果作用,我们将通过 16S rRNA 测序鉴定的 SAD 患者的微生物群移植到小鼠体内,与健康对照组相比,这些患者的微生物群组成存在差异。尽管接受 SAD 微生物群的小鼠在一系列旨在评估抑郁和一般焦虑样行为的测试中表现出正常的行为,但它们对社交恐惧(SAD 的一种模型)具有特定的高度敏感性。这种明显的社交恐惧反应伴随着中央和外周免疫功能以及终纹床核催产素表达的变化。这项工作证明了社交恐惧反应的跨界基础,并提出了微生物组作为 SAD 潜在治疗靶点的可能性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/864a/10769841/de7150f8662b/pnas.2308706120fig01.jpg

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