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Effectiveness of a hydroxynaphthoquinone fraction from Arnebia euchroma in rats with experimental colitis

机译:紫草中羟萘醌组分对实验性结肠炎大鼠的疗效

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摘要

AIM: To evaluate the potential effectiveness of hydroxynaphthoquinone mixture (HM) in rats with 2,4,6-trinitrobenzene sulfonic acid (TNBS)-induced colitis.METHODS: Colitis was induced by intracolonic administration of TNBS (80 mg/kg, dissolved in 50% ethanol). Rats were treated daily for 7 d with HM (2.5, 5, 10 mg/kg) and mesalazine 100 mg/kg 24 h after TNBS instillation. Disease progression was monitored daily by observation of clinical signs and body weight change. At the end of the experiment, macroscopic and histopathologic lesions of rats were scored, and myeloperoxidase (MPO) activity was determined. We also determined inflammatory cytokine tumor necrosis factor (TNF)-α level by ELISA, Western blotting and immunochemistry to explore the potential mechanisms of HM.RESULTS: After intracolonic instillation of TNBS, animals developed colitis associated with soft stool, diarrhea and marked colonic destruction. Administration of HM significantly attenuated clinical and histopathologic severity of TNBS-induced colitis in a dose-dependent manner. It abrogated body weight loss, diarrhea and inflammation, decreased macroscopic damage score, and improved histological signs, with a significant reduction of inflammatory infiltration, ulcer size and the severity of goblet cell depletion (all P < 0.05 vs TNBS alone group). HM could reduce MPO activity. In addition, it also decreased serum TNF-α level and down-regulated TNF-α expression in colonic tissue. This reduction was statistically significant when the dose of HM was 10 mg/kg (P < 0.05 vs TNBS alone group), and the effect was comparable to that of mesalazine and showed no apparent adverse effect. The underlying mechanism may be associated with TNF-α inhibition.CONCLUSION: These findings suggest that HM possesses favourable therapeutic action in TNBS-induced colitis, which provides direct pharmacological evidence for its clinical application.
机译:目的:评价羟基萘醌混合物(HM)对2,4,6-三硝基苯磺酸(TNBS)诱发的结肠炎大鼠的潜在作用。方法:结肠内注射TNBS(80 mg / kg,溶于水)引起结肠炎50%乙醇)。 TNBS滴注后24小时,每天用HM(2.5、5、10 mg / kg)和美沙拉嗪100 mg / kg每天治疗7天。通过观察临床体征和体重变化每天监测疾病进展。在实验结束时,对大鼠的宏观和组织病理学损伤进行评分,并测定髓过氧化物酶(MPO)活性。我们还通过ELISA,Western印迹和免疫化学方法确定了炎症细胞因子肿瘤坏死因子(TNF)-α水平,以探索HM的潜在机制。结果:结肠内滴注TNBS后,动物发展出与软便,腹泻和明显结肠破坏相关的结肠炎。 HM的给药以剂量依赖性方式显着降低了TNBS诱发的结肠炎的临床和组织病理学严重程度。它消除了体重减轻,腹泻和炎症,降低了宏观损伤评分并改善了组织学体征,并明显减少了炎症浸润,溃疡大小和杯状细胞耗竭的严重程度(与单独的TNBS组相比,所有P <0.05)。 HM可以降低MPO活性。此外,它还降低了结肠组织中的血清TNF-α水平并下调了TNF-α表达。当HM剂量为10 mg / kg时,这种降低具有统计学意义(相对于单独的TNBS组,P <0.05),并且该效果与美沙拉嗪相当,并且没有明显的不良反应。结论:HM在TNBS诱导的结肠炎中具有良好的治疗作用,为其临床应用提供了直接的药理学证据。

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