Pang Yu, Zhang Pei-Chun, Lu Rui-Rui, Li Hong-Lian, Li Ji-Cheng, Fu Hong-Xin, Cao Yi-Wen, Fang Guo-Xing, Liu Bi-Hao, Wu Jun-Biao, Zhou Jiu-Yao, Zhou Yuan
School of Pharmaceutical Sciences, Guangzhou University of Chinese Medicine, Guangzhou, China.
Department of Urology, The Sixth Affiliated Hospital of Sun Yat-Sen University, Guangzhou, China.
Front Pharmacol. 2020 Sep 3;11:541426. doi: 10.3389/fphar.2020.541426. eCollection 2020.
Acute kidney injury (AKI) is a serious disease characterized by a rapid decline in kidney function. Oxidative stress is the primary pathogenesis of AKI. Salvianolic acid B (SalB), a water-soluble compound extracted from , possesses a potent antioxidant activity. Here, we investigated the protective effect of SalB against renal ischemia-reperfusion injury (I/R) in mice. Briefly, by analyzing renal function, oxidative stress markers and inflammatory biomarkers, we found that SalB could improve kidney damage, reduce oxidative stress and inflammatory factor levels. Interestingly, the expression of the NLR family pyrin domain-containing 3 (NLRP3), caspase-1, pyroptosis related proteins gasdermin D (GSDMD) and interleukin (IL)-1β, which were significantly upregulated in the kidney tissues of I/R group, was effectively reversed by SalB. Meanwhile, renal tubular epithelial cells hypoxia and reoxygenation model was used to explore pyroptosis of caspase-1-dependent. Further mechanism study showed that the SalB pretreatment could promote the increase of nuclear factor erythroid-2 related factor 2 (Nrf2) nuclear accumulation, which significantly suppressed oxidative stress, proinflammatory cytokines, NLRP3 inflammasome activation and pyroptosis. These results indicate that SalB can inhibit caspase-1/GSDMD-mediated pyroptosis by activating Nrf2/NLRP3 signaling pathway, resulting in alleviating I/R injury in mice.
急性肾损伤(AKI)是一种以肾功能迅速下降为特征的严重疾病。氧化应激是AKI的主要发病机制。丹酚酸B(SalB)是从[具体来源未给出]中提取的一种水溶性化合物,具有强大的抗氧化活性。在此,我们研究了SalB对小鼠肾缺血再灌注损伤(I/R)的保护作用。简而言之,通过分析肾功能、氧化应激标志物和炎症生物标志物,我们发现SalB可以改善肾脏损伤,降低氧化应激和炎症因子水平。有趣的是,I/R组肾组织中显著上调的含NLR家族pyrin结构域蛋白3(NLRP3)、半胱天冬酶-1、焦亡相关蛋白gasdermin D(GSDMD)和白细胞介素(IL)-1β的表达被SalB有效逆转。同时,利用肾小管上皮细胞缺氧复氧模型探讨半胱天冬酶-1依赖性焦亡。进一步的机制研究表明,SalB预处理可促进核因子红细胞2相关因子2(Nrf2)核内蓄积增加,显著抑制氧化应激、促炎细胞因子、NLRP3炎性小体激活和焦亡。这些结果表明,SalB可通过激活Nrf2/NLRP3信号通路抑制半胱天冬酶-1/GSDMD介导的焦亡,从而减轻小鼠I/R损伤。