首页> 外文OA文献 >3-(1H-Benzodimidazol-6-yl)-5-(4-fluorophenyl)-1,2,4-oxadiazole (DDO7232), a Novel Potent Nrf2/ARE Inducer, Ameliorates DSS-Induced Murine Colitis and Protects NCM460 Cells against Oxidative Stress via ERK1/2 Phosphorylation
【2h】

3-(1H-Benzodimidazol-6-yl)-5-(4-fluorophenyl)-1,2,4-oxadiazole (DDO7232), a Novel Potent Nrf2/ARE Inducer, Ameliorates DSS-Induced Murine Colitis and Protects NCM460 Cells against Oxidative Stress via ERK1/2 Phosphorylation

机译:3-(1H-苯并D咪唑-6-基)-5-(4-氟苯基)-1,2,4-氧代唑(DDO7232),一种新型强度NRF2 /是诱导剂,改善DSS诱导的小鼠结肠炎和通过ERK1 / 2磷酸化保护NCM460细胞免受氧化应激

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

Ulcerative colitis (UC) is a common inflammatory bowel disease that can destroy the integrity of the colon and increase the risk of colorectal cancer. Oxidative stress is one of the critical pathogenic factors for UC, further impairing the entire affected colon. The Nrf2-ARE signaling pathway plays an important role in counteracting oxidative and electrophilic stress. Activation of the Nrf2-ARE pathway provides an indispensable defense mechanism for the treatment of UC. In this study, we identified a novel effective Nrf2 activator, DDO7232, which showed protective effects on NCM460 cells and therapeutic effects on DSS-induced colitis in mice. Mechanistic studies indicated that the Nrf2-ARE-inducing activity of DDO7232 was based on the activation of the ERK1/2 phosphorylation. The phosphorylation of Nrf2 Ser40 by p-ERK triggered the transport of Nrf2 into the nucleus and drove the expression of Nrf2-dependent antioxidant proteins. These results not only revealed the antioxidant mechanisms of DDO7232 but also provided an effective therapeutic option for the treatment of UC.
机译:溃疡性结肠炎(UC)是一种常见的炎症性肠疾病,可以破坏结肠的完整性并增加结直肠癌的风险。氧化应激是UC的关键致病因子之一,进一步损害整个受影响的结肠。 NRF2是信号通路在抵消氧化和亲电子应激方面起着重要作用。 NRF2的活化是途径为UC的治疗提供不可缺少的防御机制。在这项研究中,我们确定了一种新型有效的NRF2活化剂DDO7232,其对NCM460细胞的保护作用和对小鼠中DSS诱导的结肠炎的治疗作用。机械研究表明,DDO7232的NRF2诱导活性基于ERK1 / 2磷酸化的活化。通过P-ERK磷酸化NRF2 SER40将NRF2的转运触发到细胞核中并推动NRF2依赖性抗氧化蛋白的表达。这些结果不仅揭示了DDO7232的抗氧化机理,而且还提供了用于治疗UC的有效治疗选择。

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