Jiaolong capsule protects SD rats against 2,4,6-trinitrobenzene sulfonic acid induced colitis

被引:2
|
作者
Li, Yuhua [1 ,2 ]
Sun, Yang [4 ]
Diao, Fanrong [5 ]
Ruan, Yiming [3 ]
Chen, Gui'e [3 ]
Tang, Tianle [4 ]
Liu, Yongsheng [4 ]
Zhou, Huiping [3 ]
Lin, Wenming [3 ]
Dong, Mingzhi [6 ]
Liu, Tieming [6 ]
Mei, Qibing [2 ,4 ]
Cai, De [1 ]
机构
[1] Guangdong Med Univ, Affiliated Hosp, Dept Pharm, Zhanjiang 524001, Guangdong, Peoples R China
[2] Southwest Med Univ, Sch Pharm, Dept Pharmacol, Lab Oncol Pharmacol, Luzhou 646000, Sichuan, Peoples R China
[3] First Naval Force Hosp Southern Theatre Command, Zhanjiang 524005, Guangdong, Peoples R China
[4] Fourth Mil Med Univ, Sch Pharm, Dept Pharmacol, State Adm Tradit Chinese Med,Key Lab Gastrointest, Xian 710032, Shaanxi, Peoples R China
[5] Naval Mil Med Univ, Changhai Hosp, Dept Cardiol, Shanghai 200433, Peoples R China
[6] Xian Zhengda Pharmaceut Co Ltd, Xian 710072, Shaanxi, Peoples R China
基金
中国国家自然科学基金;
关键词
Jiaolong capsule; Colitis; Toll like receptor 4;
D O I
10.1016/j.jep.2020.113716
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Ethnopharmacological relevance: Jiaolong capsule (JLC) was approved for the therapy of gastrointestinal diseases by the State Food and Drug Administration (SFDA) of China. It has a satisfactory curative effect in the treatment of patients with inflammatory bowel disease, however, the mechanism remains to be elucidated. Aim of the study: In current study, the effects and possible mechanisms of JLC on 2,4,6-trinitrobenzene sulfonic acid (TNBS)-induced colitis were investigated. Materials and methods: Sulfasalazine and JLC were administrated orally and initialized 6 h after TNBS enema, once a day for seven consecutive days. The effect of JLC on intestinal microbial populations and LPS/TLR-4/NF-kappa B pathway was observed and assessed. Thirty female SD rats were distributed into six groups randomly and equally, namely, control, TNBS, TNBS + sulfasalazine (625 mg/kg), and TNBS + three different doses of JLC (25, 50, and 100 mg/kg) groups. Results: The effect of JLC on restoring normal structures of colorectum and repairing colonic damage were superior to that of sulfasalazine. JLC showed a positive effect in re-balancing intestinal bacteria population of colitis, and suppressed the activation of LPS/TLR-4/NF-kappa B pathway. Conclusion: The results suggest that JLC demonstrated a beneficial effect on treating colitis in a rat model. The possible mechanisms may be through the regulatory effect of intestinal commensal bacteria and down-regulation of LPS/TLR-4/NF-kappa B pathway.
引用
收藏
页数:10
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