Taurohyodeoxycholic acid alleviates trinitrobenzene sulfonic acid induced ulcerative colitis via regulating Th1/Th2 and Th17/Treg cells balance

被引:27
|
作者
Lv, Le [1 ]
Chen, Ziyang [1 ]
Bai, Wenhui [1 ]
Hao, Jiahui [1 ]
Heng, Zhengang [1 ]
Meng, Caijin [1 ]
Wang, Lin [1 ]
Luo, Xianglan [1 ]
Wang, Xinmiao [1 ]
Cao, Yanjun [1 ,2 ]
He, Jiao [1 ,2 ]
机构
[1] Northwest Univ, Coll Life Sci, Biomed Key Lab Shaanxi Prov, Xian, Peoples R China
[2] Northwest Univ, Minist Educ, Key Lab Resource Biol & Biotechnol Western China, Xian, Peoples R China
基金
中国国家自然科学基金;
关键词
Ulcerative colitis; Taurohyodeoxycholic acid; Th1; Th2; Th17; Treg; Cytokine; INFLAMMATORY BOWEL DISEASES; BILIARY LIPID SECRETION; PULVIS FELLIS SUIS; TH17-RELATED CYTOKINES; BILE-SALT; T-CELLS; RESPONSES; TH17; CHOLESTEROL; MODELS;
D O I
10.1016/j.lfs.2023.121501
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Aims: Taurohyodeoxycholic acid (THDCA), a natural 6 alpha-hydroxylated bile acid, exhibits intestinal anti-inflammatory effects. This study aimed to explore the efficacy of THDCA on ulcerative colitis and to reveal its mechanisms of action. Main methods: Colitis was induced by intrarectal administration of trinitrobenzene sulfonic acid (TNBS) to mice. Mice in the treatment group were gavage THDCA (20, 40, and 80 mg/kg/day) or sulfasalazine (500 mg/kg/day) or azathioprine (10 mg/kg/day). The pathologic markers of colitis were comprehensively assessed. The levels of Th1-/Th2-/Th17-/Treg-related inflammatory cytokines and transcription factors were detected by ELISA, RT-PCR, and Western blotting. The balance of Th1/Th2 and Th17/Treg cells was analyzed by Flow cytometry. Key findings: THDCA significantly alleviated colitis by improving the body weight, colon length, spleen weight, histological characteristics, and MPO activity of colitis mice. THDCA reduced the secretion of Th1-/Th17-related cytokines (IFN-gamma, IL-12p70, IL-6, IL-17A, IL-21, IL-22, and TNF-alpha) and the expressions of transcription factors (T -bet, STAT4, ROR gamma t, and STAT3), but increase the production of Th2-/Treg-related cytokines (IL-4, IL-10, and TGF-beta 1) and the expressions of transcription factors (GATA3, STAT6, Foxp3, and Smad3) in the colon. Mean-while, THDCA inhibited the expressions of IFN-gamma, IL-17A, T-bet, and ROR gamma t, but improved the expression of IL-4, IL-10, GATA3, and Foxp3 in the spleen. Furthermore, THDCA restored the proportion of Th1, Th2, Th17, and Treg cells, and balanced the Th1/Th2 and Th17/Treg immune response of colitis mice. Significance: THDCA can alleviate TNBS-induced colitis via regulating Th1/Th2 and Th17/Treg balance, which may represent a promising treatment for patients with colitis.
引用
收藏
页数:11
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