首页> 美国卫生研究院文献>Scientific Reports >The Chinese herbal formula Free and Easy Wanderer ameliorates oxidative stress through KEAP1-NRF2/HO-1 pathway
【2h】

The Chinese herbal formula Free and Easy Wanderer ameliorates oxidative stress through KEAP1-NRF2/HO-1 pathway

机译:中草药配方流浪汉通过KEAP1-NRF2 / HO-1途径减轻氧化应激

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Posttraumatic stress disorder (PTSD) gains a lot of attention due to high prevalence and strong psychological upset, but the etiology remains undefined and effective treatment is quite limited. Growing studies demonstrated the involvement of oxidative stress in various psychiatry diseases, suggesting anti-oxidation therapy might be a strategy for PTSD treatment. Free and Easy Wanderer (FAEW) is a poly-herbal drug clinically used in China for hundreds of years in the treatment of psychiatric disorder. We hypothesized that FAEW exerts clinical effects through the activity against oxidative stress with fluoxetine as antidepressant control drug. Our results revealed that FAEW significantly reduced both endogenous and H2O2-induced exogenous ROS levels in the human glioblastoma T98G and neuroblastoma SH-SY5Y cell lines. Transcriptome-wide microarray analysis indicated NRF2/HO-1 as the common target of FAEW and fluoxetine. Western blotting assay proved that the two drugs promoted NRF2 release from KEAP1 in the cytoplasm and translocation to the nuclei in a KEAP1-dependent manner, the expression of the protein HO-1 increased accordingly, suggesting the participation of KEAP1-NRF2/HO-1 pathway. The chemical constituents of FAEW (i.e. paeoniflorin, baicalin) bound to KEAP1 in silico, which hence might be the effective substances of FAEW. In conclusion, FAEW counteracted H2O2-induced oxidative stress through KEAP1-NRF2/HO-1 pathway.
机译:创伤后应激障碍(PTSD)由于高患病率和强烈的心理不适而引起了很多关注,但病因仍未明确,有效的治疗方法十分有限。越来越多的研究表明氧化应激与多种精神病疾病有关,这表明抗氧化疗法可能是PTSD治疗的一种策略。自由流浪者(FAEW)是一种在中国临床上用于治疗精神疾病的聚草药药物,已有数百年历史。我们假设FAEW通过以氟西汀为抗抑郁剂控制药物对抗氧化应激的活性发挥临床作用。我们的结果表明,FAEW显着降低了人胶质母细胞瘤T98G和神经母细胞瘤SH-SY5Y细胞系中内源性和H2O2诱导的外源性ROS水平。全转录组微阵列分析表明,NRF2 / HO-1是FAEW和氟西汀的共同靶标。 Western blotting证实这两种药物促进了KRF1在细胞质中的NRF2释放并以KEAP1依赖的方式转运至细胞核,HO-1蛋白的表达相应增加,提示KEAP1-NRF2 / HO-1的参与途径。 FAEW的化学成分(即pa药苷,黄ical苷)与计算机上的KEAP1结合,因此可能是FAEW的有效物质。总之,FAEW通过KEAP1-NRF2 / HO-1途径抵消了H2O2诱导的氧化应激。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号