Cairang Nanjia, Wu Yanran, Zhi Shumeng, Tang Jiaqin, Tie Xin, Zhan Dui, Lu Guangyuan, Shi Ying, Zhao Qipeng
Department of Tibetan Medicine, University of Xizang Medicine 10 Dangre Middle Road, Chengguan District Lhasa City 850000 China
Key Laboratory of Protection, Development and Utilization of Medicinal Resources in Liupanshan Area (Ningxia Medical University), Ministry of Education, School of Pharmacy, Ningxia Medical University 1160 Shengli Street Yinchuan 750004 China
RSC Adv. 2025 Jan 13;15(2):1052-1059. doi: 10.1039/d4ra06512c. eCollection 2025 Jan 9.
The Keap1 (Kelch-like ECH-Associating Protein 1)-Nrf2 (Nuclear Factor Erythroid 2-Related Factor 2)-ARE (Antioxidant Response Element) signaling pathway plays a crucial role in the oxidative stress response and has been linked to the development and progression of various diseases. Its influence on cerebral ischemia/reperfusion (I/R) injury has garnered significant attention. In our study, we investigated the effect of compound 2, a non-covalent inhibitor of the Keap1-Nrf2 interaction, which was previously discovered by our research group. Specifically, we used 5-(3-(-(carboxymethyl)naphthalene-2-sulfonamido)phenyl)-1-ethyl-1-pyrrole-2-carboxylic acid (compound 2) to assess its therapeutic potential in a cerebral I/R injury model. The results demonstrated that compound 2 had a significant therapeutic effect, promoting the translocation of Nrf2 from the cytoplasm to the nucleus in diseased tissue. Additionally, it increased the production of key antioxidant enzymes such as superoxide dismutase (SOD), catalase (CAT), and glutathione (GSH).
Keap1( Kelch样ECH相关蛋白1)-Nrf2(核因子红细胞2相关因子2)-ARE(抗氧化反应元件)信号通路在氧化应激反应中起关键作用,并与多种疾病的发生和发展有关。其对脑缺血/再灌注(I/R)损伤的影响已引起广泛关注。在我们的研究中,我们研究了化合物2的作用,它是我们研究小组先前发现的Keap1-Nrf2相互作用的非共价抑制剂。具体而言,我们使用5-(3-(-(羧甲基)萘-2-磺酰胺基)苯基)-1-乙基-1-吡咯-2-羧酸(化合物2)来评估其在脑I/R损伤模型中的治疗潜力。结果表明,化合物2具有显著的治疗效果,可促进病变组织中Nrf2从细胞质向细胞核的转位。此外,它还增加了关键抗氧化酶如超氧化物歧化酶(SOD)、过氧化氢酶(CAT)和谷胱甘肽(GSH)的产生。