Kwon O Jun, Choo Byung Kil, Lee Joo Young, Kim Min Yeong, Shin Sung Ho, Seo Bu-Il, Seo Young-Bae, Rhee Man Hee, Shin Mi-Rae, Kim Gyo-Nam, Park Chan Hum, Roh Seong-Soo
Daegyeong Institute for Regional Program Eveluation, Global Bencheodong, Gyeongbuk Techno Park, 300, Sampungdong, Gyeongsan-si, Gyeongsangbuk-do, 712-210, Republic of Korea.
Department of Crop Agriculture and Life Science, Chonbuk National University, Jeonju, 54896, Republic of Korea.
BMC Complement Altern Med. 2016 Jan 9;16:7. doi: 10.1186/s12906-015-0974-z.
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.
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.
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.
Our findings support the therapeutic evidence for Rhei Rhizoma ameliorating the development of esophagitis via regulating inflammation through the activation of the antioxidant pathway.
大黄作为一种传统草药已被广泛用于治疗各种炎症性疾病。本研究旨在评估其对SD大鼠实验性反流性食管炎(RE)的抗炎活性。
在诱导反流性食管炎前7天,每天以125或250mg/kg体重的剂量给予大黄,并将其效果与RE对照组和正常大鼠进行比较。
组织学评估显示,给予大黄可显著改善黏膜损伤。给予大黄后,RE对照大鼠食管组织中升高的活性氧减少。RE对照大鼠在食管炎存在时表现出抗氧化相关蛋白如核因子红系2相关因子2(Nrf2)和血红素加氧酶-1(HO-1)表达水平的下调;然而,大黄治疗组的水平显著高于RE对照大鼠。此外,RE对照大鼠在食管炎存在时表现出氧化应激相关蛋白表达的上调,但给予大黄通过丝裂原活化蛋白激酶(MAPK)相关信号通路显著降低了炎症蛋白的表达。通过阻断核因子κB(NF-κB)抑制剂(IκB)α的磷酸化,调节了NF-κB激活引起的炎症介质和细胞因子的蛋白表达。
我们的研究结果支持了大黄通过激活抗氧化途径调节炎症来改善食管炎发展的治疗证据。