Chaudhary Ghanshyam, Mahajan Umesh B, Goyal Sameer N, Ojha Shreesh, Patil Chandragouda R, Subramanya Sandeep B
Department of Pharmacology, R. C. Patel Institute of Pharmaceutical Education and ResearchShirpur, District- Dhule, Maharashtra, India.
Department of Pharmacology and Therapeutics, College of Medicine and Health Sciences, United Arab Emirates UniversityPO Box 17666, Al-Ain, United Arab Emirates.
Am J Transl Res. 2017 Apr 15;9(4):1792-1800. eCollection 2017.
The protective effect of methanolic extract of Lagerstroemia speciosaleaves (LS) was evaluated against dextran sulfate sodium (DSS) induced ulcerative colitis in C57BL/6 mice. The administration of DSS (2.5% in drinking water ad libitum) in C57BL/6 mice induced ulcerative colitis in 7 days. The LS was orally administered for 7 days at daily doses of 100 and 200 mg/kg. At the end of 7 days of treatment the animals were sacrificed, colonic tissues were removed and processed for further analysis of oxidative stress, and histopathology. In DSS treated mice the oxidative stress markers were elevated compared to controls. There was also significant reduction in the anti-oxidant defense levels marked by reduced cellular glutathione, catalase, and superoxide dismutase. The DSS-induced damage to the colon epithelium was evident from a significant increase in the lipid peroxidation. The histology of colon sections revealed inflammatory changes and marked impairment in the integrity of the mucosal lining with inflammatory changes. Both the doses of LS significantly prevented DSS-induced inflammatory and ulcerative damages of the colon, reduced lipid peroxidation and also restored the levels of innate antioxidants in the colon tissue. These findings indicate the protective effects of LS against the DSS-induced inflammatory and oxidative damage in the mouse colon. Further investigation involving bioactivity guided fractionation of the LS can yield potent constituent which may have a significant role in the treatment of inflammatory bowel disease and ulcerative colitis.
评估了紫薇叶甲醇提取物(LS)对葡聚糖硫酸钠(DSS)诱导的C57BL/6小鼠溃疡性结肠炎的保护作用。在C57BL/6小鼠中自由饮用含2.5% DSS的饮用水7天可诱导溃疡性结肠炎。LS以每日100和200 mg/kg的剂量口服给药7天。在治疗7天结束时,处死动物,取出结肠组织并进行处理,以进一步分析氧化应激和组织病理学。与对照组相比,DSS处理的小鼠氧化应激标志物升高。以细胞内谷胱甘肽、过氧化氢酶和超氧化物歧化酶减少为标志的抗氧化防御水平也显著降低。脂质过氧化显著增加表明DSS对结肠上皮造成了损伤。结肠切片的组织学显示有炎症变化,黏膜内衬完整性明显受损并有炎症改变。两种剂量的LS均能显著预防DSS诱导的结肠炎症和溃疡性损伤,减少脂质过氧化,并恢复结肠组织中天然抗氧化剂的水平。这些发现表明LS对DSS诱导的小鼠结肠炎症和氧化损伤具有保护作用。进一步涉及LS生物活性导向分级分离的研究可能会产生在炎症性肠病和溃疡性结肠炎治疗中具有重要作用的有效成分。