GABA-producing Lactococcus lactis alleviates gut dysfunction and neurobehavioral abnormalities associated with irritable bowel syndrome.

IF 5.2
Microbiome research reports Pub Date : 2025-09-23 eCollection Date: 2025-01-01 DOI:10.20517/mrr.2025.56
Zhiying Jin, Mengyu Chen, Lanxi Ao, Jingyu Wang, Jingge Sun, Xin Qian, Peijun Tian, Hao Zhang
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Abstract

Aim: This study aimed to screen Lactococcus lactis strains with varying gamma-aminobutyric acid (GABA) production and evaluate their effects on intestinal dysfunction and neurobehavioral abnormalities in an irritable bowel syndrome (IBS) mouse model, with a focus on GABAergic signaling and dose-dependent mechanisms. Methods: Three Lactococcus lactis strains were selected based on GABA yield and genetic analysis. IBS was induced in mice via Citrobacter rodentium infection and water avoidance stress. Intestinal integrity, inflammation, histopathology, and behavior were assessed. GABA levels in the colon and serum were measured by liquid chromatography-mass spectrometry (LC-MS). GABA receptor subunit expression in the colon, hippocampus, and amygdala was analyzed via quantitative real-time polymerase chain reaction and Western blotting. Results: GABA-producing strains alleviated intestinal dysfunction in IBS mice by reducing IL-6 gene expression and iNOS activity, upregulating CLDN2, and improving tissue integrity. Anxiety-like behaviors and cognitive deficits were also attenuated. Colonic GABA levels, GABRA13 mRNA, and GABRA3 protein expression increased in a dose-dependent manner, whereas TRPV1 mRNA and TRPV1 protein levels were downregulated. Serum GABA remained unchanged. In the central nervous system, the expression of hippocampal GABAA and GABAB receptors was elevated, with both GABRA13 mRNA and GABRA3 protein levels positively correlating with colonic GABA concentrations. GABRA15 expression was upregulated in the amygdala. Conclusion: GABA-producing Lactococcus lactis effectively alleviates IBS-related intestinal dysfunction and neurobehavioral abnormalities by coordinately modulating GABAergic signaling in both the gut and the central nervous system, exhibiting a clear dose-dependent effect across multiple key phenotypes.

产氨基丁酸乳球菌缓解肠易激综合征相关的肠道功能障碍和神经行为异常。
目的:本研究旨在筛选具有不同γ -氨基丁酸(GABA)产生的乳酸乳球菌菌株,并评估其对肠易激综合征(IBS)小鼠模型肠道功能障碍和神经行为异常的影响,重点研究GABA能信号传导和剂量依赖机制。方法:对3株乳酸乳球菌进行GABA产率和遗传分析。小鼠通过啮齿柠檬酸杆菌感染和避水应激诱导肠易激综合征。评估肠道完整性、炎症、组织病理学和行为。采用液相色谱-质谱法(LC-MS)测定结肠和血清中GABA水平。通过实时定量聚合酶链反应和Western blotting分析结肠、海马和杏仁核中GABA受体亚基的表达。结果:产gaba菌株通过降低IL-6基因表达和iNOS活性,上调CLDN2,改善组织完整性,减轻IBS小鼠肠道功能障碍。类似焦虑的行为和认知缺陷也有所减轻。结肠GABA水平、GABRA13 mRNA和GABRA3蛋白表达呈剂量依赖性增加,而TRPV1 mRNA和TRPV1蛋白水平下调。血清GABA保持不变。在中枢神经系统,海马GABAA和GABAB受体表达升高,GABRA13 mRNA和GABRA3蛋白水平与结肠GABA浓度呈正相关。GABRA15在杏仁核中表达上调。结论:产生gaba的乳酸乳球菌通过协调调节肠道和中枢神经系统的gaba能信号,有效缓解ibs相关肠道功能障碍和神经行为异常,并在多个关键表型中表现出明显的剂量依赖效应。
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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CiteScore
1.80
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silica gel 60GF254 thin-layer chromatography (TLC) plates
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