坦索罗辛和乳酸乳球菌对肝硬化大鼠模型中微生物群组成和肠道屏障功能的调节。

IF 4.8 2区 医学 Q2 IMMUNOLOGY
Frontiers in Cellular and Infection Microbiology Pub Date : 2025-09-02 eCollection Date: 2025-01-01 DOI:10.3389/fcimb.2025.1624065
Silvia Valeria Padilla-García, Abraham Loera-Muro, Martín Humberto Muñoz-Ortega, David Alejandro Hernández-Marín, Javier Ventura-Juárez, Sandra Luz Martínez-Hernández
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引用次数: 0

摘要

肝硬化的病理进展破坏了肝肠轴。乳酸乳球菌(Lactococcus lactis)具有免疫调节特性和增强肠道屏障功能的能力。坦索罗辛在肝损伤模型中具有抗纤维化和抗炎作用。本研究评估坦索罗辛和乳酸乳杆菌联合治疗对Wistar大鼠肝硬化模型中微生物群恢复和肠道屏障完整性的影响。材料与方法:雄性Wistar大鼠腹腔注射CCl4 4周。随后,大鼠口服坦索罗辛、乳酸乳杆菌或两者并用2周。采用16S rRNA基因测序法评估肠道菌群。采用qPCR和Western blot检测ZO-1、occludin和claudin-2蛋白的完整性。通过内毒素浓度、细菌DNA和肠外组织微生物培养来评估细菌易位。最后,分析肝脏、肠道组织学和肝功能指标。结果:乳酸菌及其与坦索罗辛(T/L)联用。乳酸菌)增加了微生物多样性,促进了肠道微生物群的平衡,其特征是厚壁菌门占优势,其次是变形菌门,梭菌门和γ变形菌门水平降低。L. lactis组上调ZO-1和occludin的表达,而坦索罗辛和T/L组未见明显变化。然而,Actis组的肠道形态与健康对照组相似。细菌易位分析显示肠外组织中没有内毒素、细菌DNA或细菌。两种治疗均改善了肝脏和肠道组织学,部分肝功能恢复。Conclusión:诸如减少细菌易位、降低系统内毒素水平、改善肠道形态和调节肠道微生物群组成等研究结果表明,这两种药物(乳酸乳杆菌和坦索罗辛),特别是联合使用,对肝硬化患者的肠道屏障发挥积极作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Microbiota composition and intestinal barrier function modulated by tamsulosin and Lactococcus lactis in a cirrhosis rat model.

Introduction: The pathological progression of cirrhosis disrupts the gut-liver axis. Lactococcus lactis (L. lactis) exhibits immunomodulatory properties and an ability to enhance intestinal barrier function. It has been demonstrated that tamsulosin has antifibrotic and anti-inflammatory effects in hepatic injury models. This study evaluated the effect of a tamsulosin and L. lactis co-treatment on the recovery of microbiota and intestinal barrier integrity in a Wistar rat liver cirrhosis model.

Material and methods: Male Wistar rats were administered CCl4 intraperitoneally for 4 weeks. Subsequently, rats received tamsulosin, L. lactis, or both, orally for 2 weeks. The intestinal microbiota was assessed using 16S rRNA gene sequencing. Intestinal barrier integrity was evaluated using qPCR and Western blot for proteins ZO-1, occludin, and claudin-2. Bacterial translocation was evaluated by endotoxin concentration, bacterial DNA, and microbial culture of extraintestinal tissues. Finally, hepatic, intestinal histology, and liver function markers were analyzed.

Results: L. lactis and its combination with tamsulosin (T/L. lactis) increased microbial diversity and promoted a balanced gut microbiota characterized by a Firmicutes predominance followed by Proteobacteria and reduced Clostridia and Gammaproteobacteria levels. L. lactis group upregulated ZO-1 and occludin expression, while no significant changes were observed with tamsulosin or T/L. actis groups, nonetheless, intestinal morphology resembled that of healthy controls. Bacterial translocation analysis revealed no endotoxins, bacterial DNA, or bacteria in extraintestinal tissues. Both treatments also improved hepatic and intestinal histology, with partial liver function recovery.

Conclusión: Findings such as reduced bacterial translocation, lower systemic endotoxin levels, improved intestinal morphology, and modulation of gut microbiota composition suggest that both agents (L. lactis and tamsulosin), particularly in combination, exert positive effects on the intestinal barrier in cirrhosis.

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来源期刊
CiteScore
7.90
自引率
7.00%
发文量
1817
审稿时长
14 weeks
期刊介绍: Frontiers in Cellular and Infection Microbiology is a leading specialty journal, publishing rigorously peer-reviewed research across all pathogenic microorganisms and their interaction with their hosts. Chief Editor Yousef Abu Kwaik, University of Louisville is supported by an outstanding Editorial Board of international experts. This multidisciplinary open-access journal is at the forefront of disseminating and communicating scientific knowledge and impactful discoveries to researchers, academics, clinicians and the public worldwide. Frontiers in Cellular and Infection Microbiology includes research on bacteria, fungi, parasites, viruses, endosymbionts, prions and all microbial pathogens as well as the microbiota and its effect on health and disease in various hosts. The research approaches include molecular microbiology, cellular microbiology, gene regulation, proteomics, signal transduction, pathogenic evolution, genomics, structural biology, and virulence factors as well as model hosts. Areas of research to counteract infectious agents by the host include the host innate and adaptive immune responses as well as metabolic restrictions to various pathogenic microorganisms, vaccine design and development against various pathogenic microorganisms, and the mechanisms of antibiotic resistance and its countermeasures.
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