两歧双歧杆菌CCFM1163通过激活BDNF-TrkB-PLC/IP3通路重建肠神经和肠屏障来缓解泻性结肠。

IF 5.1 1区 农林科学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Food & Function Pub Date : 2025-02-07 DOI:10.1039/D4FO05835F
Shengnan Zhu, Qiangqing Yu, Yifan Xue, Jiazhen Li, Yin Huang, Wenxu Liu, Gang Wang, Linlin Wang, Qixiao Zhai, Jianxin Zhao, Hao Zhang and Wei Chen
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引用次数: 0

摘要

导读:泻性结肠(CC)是一种慢性便秘,由患者长期使用刺激性泻药引起。益生菌在控制便秘方面起着至关重要的作用。目的:本研究旨在鉴定能够缓解CC的益生菌,并探讨其具体的作用机制。方法:采用番泻叶提取物建立cc模型。采用两歧双歧杆菌对小鼠进行干预。然后用ELISA和RT-qPCR检测相关标志物的变化。利用16S rDNA测序对肠道微生物进行功能预测,采用气相色谱-质谱分析测定粪便中短链脂肪酸(SCFAs)的含量。结果:泻泻菌在诱导CC的过程中损害肠神经和肠屏障,而两歧双歧杆菌CCFM1163可能通过改变肠道菌群组成(如增加乳杆菌和拟杆菌,减少粪足菌群)和提高SCFA水平(如乙酸和异丁酸)来增强结肠中脑源性神经营养因子(BDNF)的表达。随后,BDNF表达升高激活BDNF-酪氨酸激酶受体b -磷脂酶C/肌醇三磷酸(BDNF- trkb - plc /IP3)通路,上调Uchl1、S100β和Acta2的基因表达;修复肠神经系统- cajal -平滑肌细胞(ENS-ICC-SMC)网络间质细胞;上调Ocln和Tjp1基因的表达;改善CC小鼠肠道通透性;并通过上调Tlr4、下调Il1b、上调Il10来调节免疫应答,最终缓解CC。结论:两歧双歧杆菌CCFM1163是一种能够促进结肠BDNF表达,激活BDNF- trkb - plc /IP3信号通路,有效缓解CC的益生菌。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Bifidobacterium bifidum CCFM1163 alleviates cathartic colon by activating the BDNF-TrkB-PLC/IP3 pathway to reconstruct the intestinal nerve and barrier

Bifidobacterium bifidum CCFM1163 alleviates cathartic colon by activating the BDNF-TrkB-PLC/IP3 pathway to reconstruct the intestinal nerve and barrier

Introduction: Cathartic colon (CC) is a type of slow-transit constipation caused by a patient's long-term use of irritating laxatives. Probiotics play a crucial role in managing constipation. Objectives: This study aims to identify probiotics that can alleviate CC and explore their specific mechanisms of action. Methods: The CC-model was constructed using senna leaf extract. Bifidobacterium bifidum was applied to the mice for intervention. Relevant marker changes were then examined using ELISA and RT-qPCR. Furthermore, 16S rDNA sequencing was utilized for functional prediction of intestinal microorganisms, while GC-MS analysis was performed to determine the content of short-chain fatty acids (SCFAs) in feces. Results: Senna damages the intestinal nerve and the intestinal barrier while inducing CC. In contrast, Bifidobacterium bifidum CCFM1163 may enhance the brain-derived neurotrophic factor (BDNF) expression in the colon by altering the intestinal microbiota composition (e.g., increasing Lactobacillus and Bacteroides, and decreasing Faecalibaculum) and by elevating SCFA levels (e.g., acetic and isobutyric acid). Subsequently, elevated BDNF expression activates the BDNF-tyrosine kinase receptor B-phospholipase C/inositol trisphosphate (BDNF-TrkB-PLC/IP3) pathway, which upregulates the gene expression of Uchl1, S100β, and Acta2; repairs the enteric nervous system-interstitial cells of Cajal-smooth muscle cells (ENS-ICC-SMC) network; upregulates the gene expression of Ocln and Tjp1; improves intestinal permeability in CC mice; and modulates the immune response by upregulating Tlr4, downregulating Il1b, and upregulating Il10, ultimately alleviating CC. Conclusion: Bifidobacterium bifidum CCFM1163 was identified as a probiotic that can promote BDNF expression in the colon, activate the BDNF-TrkB-PLC/IP3 signaling pathway, and effectively alleviate CC.

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来源期刊
Food & Function
Food & Function BIOCHEMISTRY & MOLECULAR BIOLOGY-FOOD SCIENCE & TECHNOLOGY
CiteScore
10.10
自引率
6.60%
发文量
957
审稿时长
1.8 months
期刊介绍: Food & Function provides a unique venue for physicists, chemists, biochemists, nutritionists and other food scientists to publish work at the interface of the chemistry, physics and biology of food. The journal focuses on food and the functions of food in relation to health.
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