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粪菌移植通过改善瓦斯爆炸致创伤性脑损伤雄性大鼠的肠道微生物群组成和屏障功能来减轻认知障碍。

Fecal microbiota transplantation alleviates cognitive impairment by improving gut microbiome composition and barrier function in male rats of traumatic brain injury following gas explosion.

作者信息

Dong Xinwen, Su Yaguang, Luo Zheng, Li Cuiying, Gao Jie, Han Xiaofeng, Yao Sanqiao, Wu Weidong, Tian Linqiang, Bai Yichun, Wang Guizhi, Ren Wenjie

机构信息

Department of Environmental and Occupational Health, School of Public Health, Xinxiang Medical University, Xinxiang, China.

Institute of Trauma and Orthopedics, Xinxiang Medical University, Xinxiang, China.

出版信息

Front Microbiol. 2024 Nov 1;15:1485936. doi: 10.3389/fmicb.2024.1485936. eCollection 2024.

DOI:10.3389/fmicb.2024.1485936
PMID:39552646
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11564976/
Abstract

BACKGROUND

Dysbiosis of gut microbiota (GM) is intricately linked with cognitive impairment and the incidence of traumatic brain injury (TBI) in both animal models and human subjects. However, there is limited understanding of the impact and mechanisms of fecal microbiota transplantation (FMT) on brain and gut barrier function in the treatment of TBI induced by gas explosion (GE).

METHODS

We have employed FMT technology to establish models of gut microbiota dysbiosis in male rats, and subsequently conducted non-targeted metabolomics and microbiota diversity analysis to explore the bacteria with potential functional roles.

RESULTS

Hematoxylin-eosin and transmission electron microscopy revealed that GE induced significant pathological damage and inflammation responses, as well as varying degrees of mitochondrial impairment in neuronal cells in the brains of rats, which was associated with cognitive decline. Furthermore, GE markedly elevated the levels of regulatory T cell (Tregs)-related factors interleukin-10, programmed death 1, and fork head box protein P3 in the brains of rats. Similar changes in these indicators were also observed in the colon; however, these alterations were reversed upon transfer of normal flora into the GE-exposed rats. Combined microbiome and metabolome analysis indicated up-regulation of and , along with activation of fatty acid biosynthesis after FMT. Correlation network analysis indirectly suggested a causal relationship between FMT and alleviation of GE-induced TBI. FMT improved intestinal structure and up-regulated expression of tight junction proteins Claudin-1, Occludin, and ZO-1, potentially contributing to its protective effects on both brain and gut.

CONCLUSION

Transplantation of gut microbiota from healthy rats significantly enhanced cognitive function in male rats with traumatic brain injury caused by a gas explosion, through the modulation of gut microbiome composition and the improvement of both gut and brain barrier integrity via the gut-brain axis. These findings may offer a scientific foundation for potential clinical interventions targeting gas explosion-induced TBI using FMT.

摘要

背景

在动物模型和人类受试者中,肠道微生物群(GM)失调与认知障碍以及创伤性脑损伤(TBI)的发生率密切相关。然而,对于粪便微生物群移植(FMT)在治疗气体爆炸(GE)所致TBI时对脑和肠屏障功能的影响及机制,人们了解有限。

方法

我们采用FMT技术在雄性大鼠中建立肠道微生物群失调模型,随后进行非靶向代谢组学和微生物群多样性分析,以探索具有潜在功能作用的细菌。

结果

苏木精-伊红染色和透射电子显微镜显示,GE诱导大鼠脑内神经元细胞出现显著的病理损伤和炎症反应,以及不同程度的线粒体损伤,这与认知功能下降有关。此外,GE显著提高了大鼠脑内调节性T细胞(Tregs)相关因子白细胞介素-10、程序性死亡蛋白1和叉头框蛋白P3的水平。在结肠中也观察到这些指标的类似变化;然而,将正常菌群移植到暴露于GE的大鼠体内后,这些改变得到了逆转。微生物组和代谢组联合分析表明,FMT后 和 上调,脂肪酸生物合成激活。相关性网络分析间接表明FMT与减轻GE诱导的TBI之间存在因果关系。FMT改善了肠道结构,上调了紧密连接蛋白Claudin-1、Occludin和ZO-1的表达,这可能有助于其对脑和肠的保护作用。

结论

健康大鼠的肠道微生物群移植通过调节肠道微生物组组成以及通过肠-脑轴改善肠和脑屏障完整性,显著增强了因气体爆炸导致创伤性脑损伤的雄性大鼠的认知功能。这些发现可能为使用FMT针对气体爆炸所致TBI进行潜在临床干预提供科学依据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f280/11564976/3bc18f50045b/fmicb-15-1485936-g009.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f280/11564976/4132ff861f52/fmicb-15-1485936-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f280/11564976/e342d27ba1aa/fmicb-15-1485936-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f280/11564976/3f82995e237d/fmicb-15-1485936-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f280/11564976/3bc18f50045b/fmicb-15-1485936-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f280/11564976/ee107b1bf43a/fmicb-15-1485936-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f280/11564976/f73c20800cc6/fmicb-15-1485936-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f280/11564976/7bfc439be85b/fmicb-15-1485936-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f280/11564976/45693aa5946a/fmicb-15-1485936-g004.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f280/11564976/4132ff861f52/fmicb-15-1485936-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f280/11564976/e342d27ba1aa/fmicb-15-1485936-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f280/11564976/3f82995e237d/fmicb-15-1485936-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f280/11564976/3bc18f50045b/fmicb-15-1485936-g009.jpg

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