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Gastroprotective effects of arctigenin of Arctium lappa L. on a rat model of gastric ulcers

机译:牛Arc子中胃泌素原对胃溃疡大鼠模型的胃保护作用

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摘要

In the present study, the gastroprotective effects of arctigenin of Fructus Arctii were evaluated and the possible underlying mechanisms of action were elucidated. Arctigenin (high-performance liquid chromatography purity, >99.0%) was isolated and purified from the seeds of Arctium lappa L. The anti-ulcerogenic activity of arctigenin against ulcers induced by absolute ethanol and acetic acid was evaluated in a Sprague-Dawley rat model. In addition, the antioxidant activity was assessed by measuring malondialdehyde (MDA) levels in an ethanol-induced model and the anti-inflammatory effects were assessed by measuring five factors in an acetic acid-induced model. In the ethanol-induced model, arctigenin inhibited gastric lesions in a dose-dependent manner, by 53.04, 53.91 and 64.43% at doses of 0.05, 0.15 and 0.45 mg/kg, respectively. In addition, arctigenin reduced MDA (P<0.01) and increased superoxide dismutase (P<0.01) levels in serum when compared with the vehicle group. The lesion index induced by acetic acid was significantly inhibited by all doses of arctigenin (0.05, 0.15 and 0.45 mg/kg; P<0.01) in comparison to the vehicle group and in a dose-dependent manner. In addition, it was shown that the expression levels of tumor necrosis factor-α, interleukin-6 (IL-6), IL-10 and C-reactive protein were significantly decreased (P<0.05) in the arctigenin group compared with the vehicle group. Thus, the current study indicated that arctigenin exerted anti-ulcer activity, which may be associated with its reduction in oxidative and inflammatory damage. All the results indicate that arctigenin may be used as an effective therapeutic agent to prevent gastric ulcers.
机译:在本研究中,评价了Arctii对arc果的胃保护作用,并阐明了可能的潜在作用机理。从牛t种子中分离并纯化了牛ti皂苷元(高效液相色谱纯度,> 99.0%)。在Sprague-Dawley大鼠模型中评估了牛ti皂苷元对无水乙醇和乙酸诱导的溃疡的抗溃疡活性。另外,通过在乙醇诱导的模型中测量丙二醛(MDA)水平来评估抗氧化活性,并通过测量在乙酸诱导的模型中的五个因素来评估抗炎作用。在乙醇诱导的模型中,arggengenin剂量依赖性地抑制胃部病变,剂量分别为0.05、0.15和0.45 mg / kg时分别抑制53.04%,53.91%和64.43%。此外,与媒介物组相比,arctigenin降低了血清中的MDA(P <0.01)和增加了超氧化物歧化酶(P <0.01)。与赋形剂组相比,所有剂量的artigenin(0.05、0.15和0.45 mg / kg; P <0.01)均显着抑制了乙酸诱导的病变指数。另外,与载剂相比,arctigenin组的肿瘤坏死因子-α,白细胞介素-6(IL-6),IL-10和C反应蛋白的表达水平明显降低(P <0.05)。组。因此,当前的研究表明,arctigenin具有抗溃疡活性,这可能与其抗氧化和炎性损伤的作用有关。所有结果表明,arctigenin可用作预防胃溃疡的有效治疗剂。

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