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Compound-42 alleviates acute kidney injury by targeting RIPK3-mediated necroptosis
British Journal of Pharmacology ( IF 6.8 ) Pub Date : 2023-05-30 , DOI: 10.1111/bph.16152
Xiao-Yan He 1 , Fang Wang 1, 2 , Xiao-Guo Suo 1 , Ming-Zhen Gu 1 , Jia-Nan Wang 1 , Chuan-Hui Xu 1 , Yu-Hang Dong 1 , Yuan He 1 , Yao Zhang 1 , Ming-Lu Ji 1 , Ying Chen 1 , Meng-Meng Zhang 1 , Yin-Guang Fan 3 , Jia-Gen Wen 1 , Juan Jin 4 , Jie Wang 1 , Jun Li 1 , Chun-Lin Zhuang 5 , Ming-Ming Liu 1 , Xiao-Ming Meng 1
Affiliation  

Necroptosis plays an essential role in acute kidney injury and is mediated by receptor-interacting protein kinase 1 (RIPK1), receptor-interacting protein kinase 3 (RIPK3), and mixed lineage kinase domain-like pseudokinase (MLKL). A novel RIPK3 inhibitor, compound 42 (Cpd-42) alleviates the systemic inflammatory response. The current study was designed to investigate whether Cpd-42 exhibits protective effects on acute kidney injury and reveal the underlying mechanisms.

中文翻译:

化合物 42 通过靶向 RIPK3 介导的坏死性凋亡减轻急性肾损伤

坏死性凋亡在急性肾损伤中发挥重要作用,由受体相互作用蛋白激酶 1 (RIPK1)、受体相互作用蛋白激酶 3 (RIPK3) 和混合谱系激酶结构域样假激酶 (MLK​​L) 介导。化合物 42 (Cpd-42) 是一种新型 RIPK3 抑制剂,可减轻全身炎症反应。本研究旨在探讨 Cpd-42 是否对急性肾损伤具有保护作用并揭示其潜在机制。
更新日期:2023-05-30
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