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Protective effect of Rhei Rhizoma on reflux esophagitis in rats via Nrf2-mediated inhibition of NF-κB signaling pathway

机译:大黄对Nrf2介导的NF-κB信号通路抑制作用对大鼠反流性食管炎的保护作用

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Background Rhei Rhizoma has been widely used as a traditional herbal medicine to treat various inflammatory diseases. The present study was conducted to evaluate its anti-inflammatory activity against experimental reflux-induced esophagitis (RE) in SD rats. Methods Rhei Rhizoma was administered at 125 or 250?mg/kg body weight per day for 7?days prior to the induction of reflux esophagitis, and its effect was compared with RE control and normal rats. Results Rhei Rhizoma administration markedly ameliorated mucosal damage on histological evaluation. The elevated reactive oxygen species in the esophageal tissue of RE control rats decreased with the administration of Rhei Rhizoma. RE control rats exhibited the down-regulation of antioxidant-related proteins, such as nuclear factor-erythroid 2-related factor 2 (Nrf2) and heme oxygenase-1 (HO-1) expression levels, in the presence of esophagitis; however, the levels with Rhei Rhizoma treatment were significantly higher than those in RE control rats. Moreover, RE control rats exhibited the up-regulation of protein expressions related to oxidative stress in the presence of esophagitis, but Rhei Rhizoma administration significantly reduced the expression of inflammatory proteins through mitogen-activated protein kinase (MAPK)-related signaling pathways. The protein expressions of inflammatory mediators and cytokines by nuclear factor-kappa B (NF-κB) activation were modulated through blocking the phosphorylation of inhibitor of nuclear factor kappa B (IκB)α. Conclusion Our findings support the therapeutic evidence for Rhei Rhizoma ameliorating the development of esophagitis via regulating inflammation through the activation of the antioxidant pathway.
机译:背景大黄根已被广泛用作治疗各种炎性疾病的传统草药。进行本研究以评估其对SD大鼠实验性反流性食管炎(RE)的抗炎活性。方法在诱导反流性食管炎之前7 d,每天以125或250 mg / kg体重的剂量服用大黄,并与RE对照组和正常大鼠进行比较。结果在组织学评价上,大黄的给药明显改善了粘膜损伤。给予雷黑根后,RE对照大鼠食管组织中的活性氧升高。在患有食管炎的情况下,RE对照大鼠的抗氧化剂相关蛋白(如核因子-类胡萝卜素2相关因子2(Nrf2)和血红素加氧酶-1(HO-1))的表达水平下调。然而,Rhei Rhizoma治疗的水平显着高于RE对照大鼠。此外,RE对照大鼠在食管炎的存在下表现出与氧化应激相关的蛋白表达上调,但是Rhei Rhizoma的给药通过促分裂原激活的蛋白激酶(MAPK)相关信号通路显着降低了炎症蛋白的表达。通过阻断核因子κB(IκB)α抑制剂的磷酸化来调节核因子-κB(NF-κB)激活引起的炎症介质和细胞因子的蛋白表达。结论我们的发现支持大黄根茎通过通过激活抗氧化剂途径调节炎症来改善食道炎的治疗证据。

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