Chang Yujuan, Wei Wei, Tong Li, Liu Yanjun, Zhou Aimin, Chen Jiande, Wei Ruhan, Zhang Ping, Su Xiaolan
Department of Postgraduate Studies, Oriental Hospital of Beijing University of Chinese Medicine, Beijing 100029, P.R. China.
Department of Gastroenterology, Wangjing Hospital of China Academy of Chinese Medical Sciences, Beijing 100102, P.R. China.
Exp Ther Med. 2017 Oct;14(4):2885-2894. doi: 10.3892/etm.2017.4892. Epub 2017 Aug 7.
Functional dyspepsia (FD) is a non-organic gastrointestinal disorder that has a marked negative impact on quality of life. Compared with conventional pharmacological therapies, the traditional Chinese medicine weikangning (WKN) is a safe and effective treatment for FD. The present study aimed to determine the molecular mechanisms underlying the efficacy of WKN. The effect of different concentrations of WKN on the proliferation of the human gastric mucosal epithelial cell line GES-1 was assessed. The optimal WKN concentration to promote cell proliferation was determined, and this concentration was used to examine the effect of WKN compared with a domperidone-treated positive control group on the antioxidant capacity of GES-1 cells. The effect of WKN treatment on the growth and antioxidant activity of GES-1 cells was also assessed following nuclear factor erythroid 2 like 2 (Nrf2) knockdown. The optimal WKN dose for promoting cell growth was determined to be 0.025 mg/ml; at this concentration the expression of the antioxidant proteins glutathione S-transferase P and superoxide dismutase 2 (SOD2) were significantly elevated (P<0.0001). Furthermore, the amount of reduced glutathione and activity of SOD2 were significantly increased (P<0.0001 and P<0.01, respectively), and malondialdehyde content was significantly decreased, compared with the controls (P<0.001). With WKN treatment, the transcription of Nrf2 and its downstream genes were significantly upregulated (P<0.01), and the level and nuclear distribution of Nrf2 protein was also markedly increased. Following Nrf2 silencing, the protective antioxidant effects of WKN treatment were impaired and GES-1 cell proliferation decreased. The results of the present study suggest that the efficacy of WKN in protecting gastric mucosal epithelial cells in FD is antioxidant-dependent and mediated by Nrf2 activation.
功能性消化不良(FD)是一种对生活质量有显著负面影响的非器质性胃肠疾病。与传统药物治疗相比,中药胃康宁(WKN)是一种治疗FD安全有效的方法。本研究旨在确定WKN疗效的分子机制。评估了不同浓度的WKN对人胃黏膜上皮细胞系GES-1增殖的影响。确定了促进细胞增殖的最佳WKN浓度,并将该浓度用于检测WKN与多潘立酮治疗的阳性对照组相比对GES-1细胞抗氧化能力的影响。在核因子红细胞2样2(Nrf2)敲低后,还评估了WKN处理对GES-1细胞生长和抗氧化活性的影响。确定促进细胞生长的最佳WKN剂量为0.025mg/ml;在此浓度下,抗氧化蛋白谷胱甘肽S-转移酶P和超氧化物歧化酶2(SOD2)的表达显著升高(P<0.0001)。此外,与对照组相比,还原型谷胱甘肽含量和SOD2活性显著增加(分别为P<0.0001和P<0.01),丙二醛含量显著降低(P<0.001)。经WKN处理后,Nrf2及其下游基因的转录显著上调(P<0.01),Nrf2蛋白的水平和核分布也显著增加。Nrf2沉默后,WKN处理的保护性抗氧化作用受损,GES-1细胞增殖减少。本研究结果表明,WKN在保护FD胃黏膜上皮细胞方面的疗效依赖于抗氧化作用,并由Nrf2激活介导。
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