Yang Bowen, Sun Tianning, Chen Yingle, Xiang Hongbing, Xiong Jun, Bao Shiting
Department of Hepatobiliary Surgery, Affiliated Hospital of Guangdong Medical University, Zhanjiang, China.
Department of Anesthesiology and Pain Medicine, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
Front Microbiol. 2022 May 10;13:909461. doi: 10.3389/fmicb.2022.909461. eCollection 2022.
The pathogenesis of Hepatic Encephalopathy (HE) is complex and multifactorial. The development of metagenomics sequencing technology led to show the significant role of gut microbiota in the pathogenesis of cognitive dysfunction, which paved the way for further research in this field. However, it is unknown whether gut microbiota plays a role in bile duct ligation (BDL)-evoked cholestatic liver disease-related cognitive dysfunction. The aim of this investigation is to assess BDL mice induced cognitive dysfunction and meanwhile to delineate the alteration of gut microbiota in cognitive dysfunction mice, which may underline the role of gut microbiota in BDL mice induced cognitive dysfunction. Our study was carried out in male C57BL/6 J mice with bile duct ligation. The liver functions were assessed different biochemical markers [alanine aminotransferase (ALT), aspartate aminotransferase (AST), alkaline phosphatase (ALP), total bilirubin (TBIL), and total bile acid (TBA)] and a histopathological examination of the liver tissue. We used the novel object recognition test (NORT) to assess cognitive dysfunction. And BDL mice were divided into BDL with cognitive dysfunction (BDL-CD) or BDL without cognitive dysfunction (BDL-NCD groups) by the result of hierarchical cluster analysis of NORT. Then, 16S ribosomal RNA (rRNA) gene sequencing was used to compare the gut bacterial composition between BDL-CD and BDL-NCD groups. According to our results, we concluded that bile duct ligation can significantly change the gut microbiota composition, and , , and play a vital role in BDL-evoked cholestatic liver disease-related cognitive dysfunction.
肝性脑病(HE)的发病机制复杂且具有多因素性。宏基因组测序技术的发展揭示了肠道微生物群在认知功能障碍发病机制中的重要作用,为该领域的进一步研究铺平了道路。然而,尚不清楚肠道微生物群是否在胆管结扎(BDL)诱发的胆汁淤积性肝病相关认知功能障碍中起作用。本研究的目的是评估BDL小鼠诱导的认知功能障碍,同时描绘认知功能障碍小鼠肠道微生物群的变化,这可能突显肠道微生物群在BDL小鼠诱导的认知功能障碍中的作用。我们的研究在雄性C57BL/6 J胆管结扎小鼠中进行。通过不同的生化标志物[丙氨酸转氨酶(ALT)、天冬氨酸转氨酶(AST)、碱性磷酸酶(ALP)、总胆红素(TBIL)和总胆汁酸(TBA)]以及肝组织的组织病理学检查来评估肝功能。我们使用新颖物体识别测试(NORT)来评估认知功能障碍。根据NORT的层次聚类分析结果,将BDL小鼠分为有认知功能障碍的BDL(BDL-CD)组或无认知功能障碍的BDL(BDL-NCD)组。然后,使用16S核糖体RNA(rRNA)基因测序来比较BDL-CD组和BDL-NCD组之间的肠道细菌组成。根据我们研究结果,我们得出结论,胆管结扎可显著改变肠道微生物群组成,且 、 和 在BDL诱发的胆汁淤积性肝病相关认知功能障碍中起至关重要的作用。 (原文此处有缺失内容,翻译按原文呈现)