Yu Daolun, Ge Kai, Chen Naidong, Wang Yue, Xu Hangbo
College of Biotechnology and Pharmaceutical Engineering, West Anhui University, Lu'an 237012, China.
College of Biotechnology and Pharmaceutical Engineering, West Anhui University, Lu'an 237012, China.
Int J Biol Macromol. 2025 Sep;321(Pt 4):146626. doi: 10.1016/j.ijbiomac.2025.146626. Epub 2025 Aug 6.
Sepsis frequently results in acute kidney injury (AKI), characterized by oxidative damage and inflammation. Polysaccharides derived from Poria cocos have significant anti-inflammatory and antioxidant effects. This study aims to investigate the role of water-soluble Poria cocos polysaccharide (WPCP) in sepsis-related renal damage by administering lipopolysaccharide (LPS) in mice. WPCP significantly reduced serum levels of BUN, creatinine, NGAL, and KIM-1, as well as renal tubular tissue damage in LPS-treated mice. WPCP was effective in reducing both the serum levels and the expression of inflammatory factors (IL-1β, IL-6, MCP-1, and TNF-α) in kidney tissue. Moreover, WPCP blocked the increase in ROS levels and caspase-3/7 activity induced by LPS, while also preventing the decrease in GSH and ATP levels. The results were also confirmed by in vitro experiments. Mechanistically, WPCP significantly suppressed LPS-induced NOX4 expression and NADPH oxidase activation. Alternatively, studies demonstrated WPCP inhibited the activation of NF-κB by preventing the phosphorylation of IκBα caused by LPS. Importantly, our findings confirmed that the activation of NF-κB signaling by LPS is involved in NADPH oxidase activation. These data suggest that WPCP mitigates LPS-induced AKI through the suppression of the NF-κB-NOX4 signaling pathway. WPCP could be a potential therapeutic option for treating sepsis-related AKI.
脓毒症常导致急性肾损伤(AKI),其特征为氧化损伤和炎症。茯苓多糖具有显著的抗炎和抗氧化作用。本研究旨在通过给小鼠注射脂多糖(LPS)来探究水溶性茯苓多糖(WPCP)在脓毒症相关肾损伤中的作用。WPCP显著降低了LPS处理小鼠的血清尿素氮、肌酐、中性粒细胞明胶酶相关脂质运载蛋白(NGAL)和肾损伤分子-1(KIM-1)水平,以及肾小管组织损伤。WPCP有效降低了肾组织中炎症因子(白细胞介素-1β、白细胞介素-6、单核细胞趋化蛋白-1和肿瘤坏死因子-α)的血清水平和表达。此外,WPCP阻断了LPS诱导的活性氧(ROS)水平升高和半胱天冬酶-3/7活性增加,同时还防止了谷胱甘肽(GSH)和三磷酸腺苷(ATP)水平降低。体外实验也证实了这些结果。机制上,WPCP显著抑制LPS诱导的NADPH氧化酶4(NOX4)表达和NADPH氧化酶激活。另外,研究表明WPCP通过阻止LPS引起的IκBα磷酸化来抑制核因子-κB(NF-κB)的激活。重要的是,我们的研究结果证实LPS激活NF-κB信号通路与NADPH氧化酶激活有关。这些数据表明WPCP通过抑制NF-κB-NOX4信号通路减轻LPS诱导的AKI。WPCP可能是治疗脓毒症相关AKI的一种潜在治疗选择。