Protective Effects of the Combination of the Herbal Compound Against Inflammation Related to Obesity and Colitis Induced by Diet in Mice

Fatemeh Azizian-Farsani, Navid Abedpoor, M. Derakhshan, M. Nasr-Esfahani, M. Sheikhha, K. Ghaedi
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引用次数: 1

Abstract

Objective: High-fat diet (HFD) rises the susceptibility of both obesity and consequently Inflammatory Bowel Disease (IBD). We designed a study to investigate the improving effects of herbal extract (HE, the combination of turmeric, ginger, boswellia, and cat’s claw extract) on the risk of high AGEs-fat diet 60% (HFD) mice induced colitis and obesity. Materials and Methods: Four-week-old C57BL/6 male mice after 2 weeks adaptation with normal diet were fed with either HFD or normal diets. After 6 weeks of being on diet, animals received HE for 16 weeks. Obesity index markers were determined as well as histological studies using H&E (Hematoxylin-eosin) staining. Colonic expression of IL-1β was determined. Data analysis was performed by utilizing Kruskal-Wallis and Mann-Whitney test for post-hoc comparisons, and SPSS (version 17.0) and GraphPad Prism Software (Version 8.0, USA). Results: HE decreased histological scores (by 6-fold) in HFD diet-fed mice, and reduced myeloperoxidase activity (by 2.2-fold), and ratio of colon weight to length (by 4-fold) in HFD diet-fed mice. Moreover, HE prevented intestinal permeability through the restoration of ZO-1 (by 4-fold) and immune homeostasis by modulation of IL-1β (by 2.4-fold) expression. Conclusion: HFD induced obesity-associated colitis. HE decreased the colitis symptoms in HFD diet-fed mice, with the reduction of inflammation.
复方中药对小鼠饮食性肥胖及结肠炎相关炎症的保护作用
目的:高脂肪饮食(HFD)增加了肥胖和炎症性肠病(IBD)的易感性。我们设计了一项研究,探讨草药提取物(姜黄、生姜、乳香草和猫爪提取物的组合)对高ages -脂肪饮食60% (HFD)小鼠诱导的结肠炎和肥胖风险的改善作用。材料与方法:4周龄C57BL/6雄性小鼠适应正常饮食2周后,分别饲喂HFD和正常饮食。节食6周后,动物接受16周的HE治疗。采用H&E(苏木精-伊红)染色测定肥胖指数标记物并进行组织学研究。测定IL-1β的结肠表达。数据分析采用Kruskal-Wallis和Mann-Whitney事后比较检验,使用SPSS(17.0版本)和GraphPad Prism软件(8.0版本,美国)。结果:HE降低了HFD喂养小鼠的组织学评分(降低了6倍),降低了HFD喂养小鼠的髓过氧化物酶活性(降低了2.2倍),降低了结肠重长比(降低了4倍)。此外,HE通过恢复ZO-1(4倍)和调节IL-1β(2.4倍)表达来阻止肠道通透性。结论:HFD诱导肥胖相关性结肠炎。HE减轻了HFD饮食喂养小鼠的结肠炎症状,同时减少了炎症。
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