Cui Mengjiao, Xu Qiming, Duan Lianxiang, Lu Jianrao, Hu Jing
Department of Nephropathy, The Seventh People's Hospital, Shanghai University of Traditional Chinese Medicine, Shanghai, 200137, People's Republic of China.
Shanghai University of Traditional Chinese Medicine, Shanghai, 201203, People's Republic of China.
Drug Des Devel Ther. 2025 Mar 6;19:1609-1626. doi: 10.2147/DDDT.S509357. eCollection 2025.
Vaccarin is a natural flavonoid glycoside with anti-inflammatory, antioxidant and nephroprotective effects. However, the effects of vaccarin on renal fibrosis (RF) and its molecular mechanisms remain unclear. This study aimed to investigate the effects of vaccarin on RF and its molecular mechanisms.
Network pharmacology was used to analyze the effect of vaccarin on RF, and molecular docking and molecular dynamics simulations were performed to assess the binding of nuclear factor erythroid 2-related factor 2 (Nrf2) to vaccarin. A mouse model of unilateral ureteral obstruction (UUO) was established in vivo, and human renal tubular epithelial (HK2) cells were induced with transforming growth factor-β (TGF-β) and RSL3, respectively, as an in vitro model. The anti-fibrotic effect of vaccarin was observed by histopathological staining and determination of fibrous markers. Changes in oxidative stress and ferroptosis-related markers were detected by kits, Western blot (WB), qRT-PCR and immunofluorescence (IF). Finally, Nrf2 inhibitors were added to the in vitro model to observe the effects on fibrosis and ferroptosis.
Vaccarin and RF cross genes are enriched for oxidative stress. Nrf2 binds stably to vaccarin. Both in vivo and in vitro experiments showed that vaccarin treatment reduced the expression of fibrosis markers, decreased the levels of reactive oxygen species (ROS), malondialdehyde (MDA), lipid peroxidation (LPO) and Fe, and increased glutathione (GSH) secretion. In addition, vaccarin down-regulated the expression of Long-chain acyl-CoA synthetase 4 (ACSL4), prostaglandin-endoperoxide synthase 2 (PTGS2) and NADPH oxidase 1 (NOX1), and up-regulated Nrf2 and its downstream solute transport family 7 member 11 (SLC7A11) and glutathione peroxidase 4 (GPX4) expression. Mechanistic studies indicated that vaccarin activated the Nrf2/SLC7A11/GPX4 pathway to inhibit ferroptosis, and this inhibition was effectively reversed by the Nrf2 inhibitor.
Vaccarin ameliorates RF by inhibiting ferroptosis via Nrf2/SLC7A11/GPX4 pathway.
vaccarin是一种具有抗炎、抗氧化和肾保护作用的天然黄酮糖苷。然而,vaccarin对肾纤维化(RF)的影响及其分子机制尚不清楚。本研究旨在探讨vaccarin对RF的影响及其分子机制。
采用网络药理学分析vaccarin对RF的作用,并进行分子对接和分子动力学模拟,以评估核因子红细胞2相关因子2(Nrf2)与vaccarin的结合。在体内建立单侧输尿管梗阻(UUO)小鼠模型,在体外分别用转化生长因子-β(TGF-β)和RSL3诱导人肾小管上皮(HK2)细胞作为体外模型。通过组织病理学染色和纤维标记物测定观察vaccarin的抗纤维化作用。用试剂盒、蛋白质免疫印迹法(WB)、qRT-PCR和免疫荧光法(IF)检测氧化应激和铁死亡相关标志物的变化。最后,在体外模型中加入Nrf2抑制剂,观察其对纤维化和铁死亡的影响。
vaccarin与RF交叉基因富含氧化应激。Nrf2与vaccarin稳定结合。体内和体外实验均表明,vaccarin处理可降低纤维化标志物的表达,降低活性氧(ROS)、丙二醛(MDA)、脂质过氧化(LPO)和铁的水平,并增加谷胱甘肽(GSH)的分泌。此外,vaccarin下调长链酰基辅酶A合成酶4(ACSL4)、前列腺素内过氧化物合酶2(PTGS2)和NADPH氧化酶1(NOX1)的表达,上调Nrf2及其下游溶质转运家族7成员11(SLC7A11)和谷胱甘肽过氧化物酶4(GPX4)的表达。机制研究表明,vaccarin激活Nrf2/SLC7A11/GPX4通路抑制铁死亡,而Nrf2抑制剂可有效逆转这种抑制作用。
vaccarin通过Nrf2/SLC7A11/GPX4通路抑制铁死亡来改善RF。