Department of Pharmacy, Affiliated Hospital of Guangdong Medical University, Zhanjiang, 524001, Guangdong, PR China; Laboratory of Oncological Pharmacology, Department of Pharmacology, School of Pharmacy, Southwest Medical University, Luzhou, 646000, Sichuan, PR China.
Key Laboratory of Gastrointestinal Pharmacology of Chinese Materia Medica of the State Administration of Traditional Chinese Medicine, Department of Pharmacology, School of Pharmacy, The Fourth Military Medical University, Xi'an, 710032, Shaanxi, PR China.
J Ethnopharmacol. 2021 Apr 6;269:113716. doi: 10.1016/j.jep.2020.113716. Epub 2021 Jan 18.
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.
In current study, the effects and possible mechanisms of JLC on 2,4,6-trinitrobenzene sulfonic acid (TNBS)-induced colitis were investigated.
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-κB 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.
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-κB pathway.
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-κB pathway.
蛟龙胶囊(JLC)已被中国国家食品药品监督管理局(SFDA)批准用于治疗胃肠道疾病。它在治疗炎症性肠病患者方面具有令人满意的疗效,但作用机制仍需阐明。
本研究旨在探讨 JLC 对 2,4,6-三硝基苯磺酸(TNBS)诱导的结肠炎的作用及其可能机制。
柳氮磺胺吡啶和 JLC 在 TNBS 灌肠后 6 小时开始口服给药,每天一次,连续 7 天。观察和评估 JLC 对肠道微生物群和 LPS/TLR-4/NF-κB 通路的影响。
将 30 只雌性 SD 大鼠随机均分为 6 组,即对照组、TNBS 组、TNBS+柳氮磺胺吡啶(625mg/kg)组和 TNBS+JLC 三个不同剂量(25、50 和 100mg/kg)组。
JLC 对恢复大肠正常结构和修复结肠损伤的作用优于柳氮磺胺吡啶。JLC 对结肠炎肠道细菌种群的平衡有积极作用,并抑制 LPS/TLR-4/NF-κB 通路的激活。
结果表明,JLC 对治疗大鼠结肠炎具有有益作用。其可能的机制可能是通过调节肠道共生细菌和下调 LPS/TLR-4/NF-κB 通路。