Tauroursodeoxycholic Acid Reverses Dextran Sulfate Sodium-Induced Colitis in Mice via Modulation of Intestinal Barrier Dysfunction and Microbiome Dysregulation.

IF 3.1 3区 医学 Q2 PHARMACOLOGY & PHARMACY
Longbiao Luo, Yi Zhao, Guangji Zhang, Sijing Dong, YinYue Xu, Hehe Shi, Menggai Zhang, Xue Liu, Sicen Wang, Hua Luo, Wanghui Jing
{"title":"Tauroursodeoxycholic Acid Reverses Dextran Sulfate Sodium-Induced Colitis in Mice via Modulation of Intestinal Barrier Dysfunction and Microbiome Dysregulation.","authors":"Longbiao Luo, Yi Zhao, Guangji Zhang, Sijing Dong, YinYue Xu, Hehe Shi, Menggai Zhang, Xue Liu, Sicen Wang, Hua Luo, Wanghui Jing","doi":"10.1124/jpet.123.002020","DOIUrl":null,"url":null,"abstract":"<p><p>Ulcerative colitis (UC) is an immune-mediated inflammatory disease that can lead to persistent damage and even cancer without any intervention. Conventional treatments can alleviate UC symptoms but are costly and cause various side effects. Tauroursodeoxycholic acid (TUDCA), a secondary bile acid derivative, possesses anti-inflammatory and cytoprotective properties for various diseases, but its potential therapeutic benefits in UC have not been fully explored. Mice were subjected to colitis induction using 3% dextran sulfate sodium (DSS). The therapeutic effect of TUDCA was evaluated by body weight loss, disease activity index (DAI), colon length, and spleen weight ratio. Tissue pathology was assessed using H&E staining, while the levels of pro-inflammatory and anti-inflammatory cytokines in colonic tissue were quantified via ELISA. Tight junction proteins were detected by immunoblotting and intestinal permeability was assessed using fluorescein isothiocyanate (FITC)-dextran. Moreover, the gut microbiota was profiled using high-throughput sequencing of the 16S rDNA gene. TUDCA alleviated the colitis in mice, involving reduced DAI, attenuated colon and spleen enlargement, ameliorated histopathological lesions, and normalized levels of pro-inflammatory and anti-inflammatory cytokines. Furthermore, TUDCA treatment inhibited the downregulation of intestinal barrier proteins, including zonula occludens-1 and occludin, thus reducing intestinal permeability. The analysis of gut microbiota suggested that TUDCA modulated the dysbiosis in mice with colitis, especially for the remarkable rise in <i>Akkermansia</i> TUDCA exerted a therapeutic efficacy in DSS-induced colitis by reducing intestinal inflammation, protecting intestinal barrier integrity, and restoring gut microbiota balance. SIGNIFICANCE STATEMENT: This study demonstrates the potential therapeutic benefits of Tauroursodeoxycholic acid (TUDCA) in ulcerative colitis. TUDCA effectively alleviated colitis symptoms in mice, including reducing inflammation, restoring intestinal barrier integrity and the dysbiosis of gut microbiota. This work highlights the promising role of TUDCA as a potentially alternative treatment, offering new insights into managing this debilitating condition.</p>","PeriodicalId":16798,"journal":{"name":"Journal of Pharmacology and Experimental Therapeutics","volume":" ","pages":"116-124"},"PeriodicalIF":3.1000,"publicationDate":"2024-06-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Pharmacology and Experimental Therapeutics","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1124/jpet.123.002020","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"PHARMACOLOGY & PHARMACY","Score":null,"Total":0}
引用次数: 0

Abstract

Ulcerative colitis (UC) is an immune-mediated inflammatory disease that can lead to persistent damage and even cancer without any intervention. Conventional treatments can alleviate UC symptoms but are costly and cause various side effects. Tauroursodeoxycholic acid (TUDCA), a secondary bile acid derivative, possesses anti-inflammatory and cytoprotective properties for various diseases, but its potential therapeutic benefits in UC have not been fully explored. Mice were subjected to colitis induction using 3% dextran sulfate sodium (DSS). The therapeutic effect of TUDCA was evaluated by body weight loss, disease activity index (DAI), colon length, and spleen weight ratio. Tissue pathology was assessed using H&E staining, while the levels of pro-inflammatory and anti-inflammatory cytokines in colonic tissue were quantified via ELISA. Tight junction proteins were detected by immunoblotting and intestinal permeability was assessed using fluorescein isothiocyanate (FITC)-dextran. Moreover, the gut microbiota was profiled using high-throughput sequencing of the 16S rDNA gene. TUDCA alleviated the colitis in mice, involving reduced DAI, attenuated colon and spleen enlargement, ameliorated histopathological lesions, and normalized levels of pro-inflammatory and anti-inflammatory cytokines. Furthermore, TUDCA treatment inhibited the downregulation of intestinal barrier proteins, including zonula occludens-1 and occludin, thus reducing intestinal permeability. The analysis of gut microbiota suggested that TUDCA modulated the dysbiosis in mice with colitis, especially for the remarkable rise in Akkermansia TUDCA exerted a therapeutic efficacy in DSS-induced colitis by reducing intestinal inflammation, protecting intestinal barrier integrity, and restoring gut microbiota balance. SIGNIFICANCE STATEMENT: This study demonstrates the potential therapeutic benefits of Tauroursodeoxycholic acid (TUDCA) in ulcerative colitis. TUDCA effectively alleviated colitis symptoms in mice, including reducing inflammation, restoring intestinal barrier integrity and the dysbiosis of gut microbiota. This work highlights the promising role of TUDCA as a potentially alternative treatment, offering new insights into managing this debilitating condition.

牛磺脱氧胆酸通过调节肠屏障功能障碍和微生物组失调逆转DSS诱导的小鼠结肠炎
背景:溃疡性结肠炎(UC)是一种免疫介导的炎症性疾病,如果不采取任何干预措施,可导致持续性损害,甚至癌变。传统治疗方法可以缓解 UC 症状,但费用昂贵,甚至会产生各种副作用。牛磺脱氧胆酸(TUDCA)是一种次级胆汁酸衍生物,对多种疾病具有抗炎和细胞保护作用,但其对 UC 的潜在治疗作用尚未得到充分探索。研究方法使用 3% 右旋糖酐硫酸钠(DSS)诱导小鼠患结肠炎。通过体重下降、疾病活动指数(DAI)、结肠长度和脾脏重量比来评估 TUDCA 的治疗效果。组织病理学采用 H&E 染色法进行评估,结肠组织中的促炎和抗炎细胞因子水平则通过酶联免疫吸附试验(ELISA)进行量化。通过免疫印迹法检测了紧密连接蛋白,并使用异硫氰酸荧光素(FITC)-葡聚糖评估了肠道通透性。此外,还利用 16S rDNA 基因的高通量测序分析了肠道微生物群。研究结果TUDCA能缓解小鼠结肠炎,包括降低DAI、减轻结肠和脾脏肿大、改善组织病理学病变、使促炎和抗炎细胞因子水平正常化。此外,TUDCA 还能抑制肠道屏障蛋白(包括 ZO-1 和闭塞素)的下调,从而降低肠道通透性。对肠道微生物群的分析表明,TUDCA 可调节结肠炎小鼠体内的菌群失调,尤其是 Akkermansia 的显著增加:TUDCA通过减轻肠道炎症、保护肠道屏障完整性和恢复肠道微生物群平衡,对DSS诱导的结肠炎具有疗效。意义声明 本研究证明了牛磺脱氧胆酸(TUDCA)对溃疡性结肠炎(UC)的潜在治疗效果。TUDCA 能有效缓解小鼠的结肠炎症状,包括减轻炎症、恢复肠道屏障完整性和肠道微生物群失调。这项工作凸显了 TUDCA 作为一种潜在替代疗法的前景,为控制这种使人衰弱的疾病提供了新的见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
CiteScore
6.90
自引率
0.00%
发文量
115
审稿时长
1 months
期刊介绍: A leading research journal in the field of pharmacology published since 1909, JPET provides broad coverage of all aspects of the interactions of chemicals with biological systems, including autonomic, behavioral, cardiovascular, cellular, clinical, developmental, gastrointestinal, immuno-, neuro-, pulmonary, and renal pharmacology, as well as analgesics, drug abuse, metabolism and disposition, chemotherapy, and toxicology.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信