Mohamed Maged E, Elsayed Sahar A, Madkor Hafez R, Eldien Heba M Saad, Mohafez Omar M
Department of Pharmaceutical Sciences, College of Clinical Pharmacy, King Faisal University, Al-Ahsa, Kingdom of Saudi Arabia.
Department of Pharmacognosy, College of Pharmacy, University of Zagazig, Zagazig, Egypt.
Intest Res. 2021 Apr;19(2):194-205. doi: 10.5217/ir.2020.00021. Epub 2020 Aug 21.
BACKGROUND/AIMS: Ulcerative colitis (UC) is a chronic inflammatory disorder with indefinite etiology; however, environmental, genetic, immune factors and microbial agents could be implicated in its pathogenesis. UC treatment is lifelong, therefore; the potential side effects and cost of the therapy are significant. Yarrow is a promising medicinal plant with the ability to treat many disorders, owing to its bioactive compounds especially the essential oil. The main aim of this research was to investigate the therapeutic effect of the yarrow oil on colitis including the involved mechanism of action.
In 21-female C57BL/6 mice were divided into 3 groups; control group, colitis model group, and oil-treated group. Groups 2 and 3 received 5% dextran sulfate sodium (DSS) in drinking water for 9 days, and concomitantly, only group 3 was given 100 mg/kg yarrow oil. Mice were examined for their body weight, stool consistency and bleeding, and the disease activity indexes were calculated.
Oral administration of yarrow oil markedly repressed the severity of UC via the reduction of the inflammatory signs and restoring colon length. The oil was able to down-regulate nuclear factor kappa light chain enhancer of activated B cells (NF-κB), up-regulate peroxisome proliferator-activated receptor gamma (PPAR-γ), and enhance transforming growth factor-β expression. The oil normalized the tumor necrosis factor-α expression, restored the normal serum level of interleukin-10 (IL-10) and reduced the serum level of IL-6.
Yarrow oil mitigated UC symptoms and regulated the inflammatory cytokines secretion via regulation of NF-κB and PPAR-γ pathways in the mice model, however, this recommendation requires further investigations using clinical studies to confirm the use of the oil on humans.
背景/目的:溃疡性结肠炎(UC)是一种病因不明的慢性炎症性疾病;然而,环境、遗传、免疫因素和微生物因子可能与其发病机制有关。UC的治疗是终身的,因此,治疗的潜在副作用和成本很高。欧蓍草是一种很有前景的药用植物,因其生物活性化合物尤其是精油,能够治疗多种疾病。本研究的主要目的是探讨欧蓍草油对结肠炎的治疗作用及其作用机制。
将21只雌性C57BL/6小鼠分为3组;对照组、结肠炎模型组和油处理组。第2组和第3组在饮用水中给予5%硫酸葡聚糖钠(DSS),持续9天,同时,仅第3组给予100mg/kg欧蓍草油。检查小鼠的体重、粪便稠度和出血情况,并计算疾病活动指数。
口服欧蓍草油通过减轻炎症体征和恢复结肠长度,显著减轻了UC的严重程度。该油能够下调活化B细胞的核因子κB轻链增强子(NF-κB),上调过氧化物酶体增殖物激活受体γ(PPAR-γ),并增强转化生长因子-β的表达。该油使肿瘤坏死因子-α表达正常化,恢复白细胞介素-10(IL-10)的正常血清水平,并降低IL-6的血清水平。
在小鼠模型中,欧蓍草油减轻了UC症状,并通过调节NF-κB和PPAR-γ途径调节炎症细胞因子的分泌,然而,这一建议需要通过临床研究进一步调查,以确认该油在人体上的应用。