| Literature DB >> 29126723 |
Lili Huang1, Jiabing Wang1, Liping Chen2, Min Zhu2, Shoubiao Wu3, Shenghui Chu2, Yuantie Zheng2, Ziliang Fan2, Jiafeng Zhang2, Wulan Li4, Dahui Chen2, Xiufei Yang5, Sicen Wang6, Peihong Qiu7, Jianzhang Wu8.
Abstract
Exogenous supplementation of antioxidants with ROS scavenging activity would be a potential therapy to cerebral ischemia-reperfusion injury in stroke. In the present study, a series of NDGA analogues with attenuation oxidative stress by directly scavenging ROS and indirectly through keap1/Nrf2/ARE pathway activation were designed and synthesized. All analogues were found to effectively remove ROS directly by DPPH radical scavenging assay, and compound 3a conferred potent protection from the oxidative injury in PC12 cells via promoting Nrf2 to translocate into nucleus and increasing expression of heme oxygenase-1(HO-1), where strongly reduced intracellular ROS level indirectly. More importantly, 3a significantly reduced brain infarction after cerebral ischemia-reperfusion injury in rats subjected to transient middle cerebral artery occlusion (MCAO). Overall, our findings shown compound 3a could serve as a promising compound for the treatment of stroke.Entities:
Keywords: Anti-ischemic stroke agent; Keap1/Nrf2/ARE pathway; ROS; Synthesis
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Year: 2017 PMID: 29126723 DOI: 10.1016/j.ejmech.2017.09.028
Source DB: PubMed Journal: Eur J Med Chem ISSN: 0223-5234 Impact factor: 6.514