Icariin protects against cisplatin-induced renal injury and ferroptosis via JNK pathway in mice
Year: 2026
Type: article
Abstract: Acute kidney injury (AKI) induced by cisplatin (DDP) is a critical complication that elevates patient mortality and worsens clinical outcomes. Recent evidence highlights ferroptosis as a key contributor to AKI pathogenesis. Icariin (ICA), a natural flavonoid glycoside with antioxidant, anti-apoptotic, and anti-ferroptotic properties, holds therapeutic potential. This study aimed to explore ICA’s protective effects against DDP-induced AKI in mice and human renal tubular epithelial (HK-2) cells, focusing on its anti-ferroptotic mechanisms. A DDP-induced AKI mouse model was established using a single intraperitoneal injection of 30 mg/kg DDP. In vitro, HK-2 cells were treated with DDP to mimic renal injury. ICA’s effects were evaluated through histopathological analysis, measurement of kidney injury markers (e.g., Scr, BUN), and assessment of oxidative stress (ROS, MDA), apoptosis (Bax, cleaved caspase-3), and ferroptosis-related markers (Fe²⁺, ACSL4, GPX4, FTH1). Mitochondrial morphology was examined via electron microscopy. Protein expression and phosphorylation of JNK signaling components were analyzed using Western blot. In mice, ICA alleviated DDP-induced tubular dilation, mucus accumulation, and epithelial shedding, and reduced levels of kidney injury markers. It suppressed apoptosis, as indicated by decreased Bax and cleaved caspase-3, reduced oxidative stress, reflected by lower ROS and MDA levels, and inhibited ferroptosis through a reduction in Fe²⁺. In HK-2 cells, ICA counteracted DDP-induced cytotoxicity, restored mitochondrial integrity, and mitigated ferroptosis, evidenced by decreased ACSL4 and increased GPX4 and FTH1. Mechanistically, ICA inhibited JNK phosphorylation in both models. Animal studies further confirmed that the renoprotective effects of ICA were mediated through modulation of the JNK pathway. ICA alleviates DDP-induced AKI by inhibiting apoptosis, oxidative stress, and ferroptosis, partially through suppression of JNK signaling. These findings underscore ICA’s potential as a therapeutic agent for DDP-associated kidney injury, with ferroptosis and JNK pathways as critical targets. ICA protects against DDP-induced AKI in mice and HK-2 cells. ICA suppresses ferroptosis by downregulating pro-ferroptotic protein ACSL4 while upregulating anti-ferroptotic proteins GPX4 and FTH1. ICA inhibits oxidative stress and apoptosis, improving renal tubular dilation and reducing kidney injury markers. ICA may exert its protective effects by inhibiting JNK protein phosphorylation. Animal experiments validate the therapeutic potential of ICA for DDP-induced AKI via the JNK pathway.
Source: BMC Nephrology
Authors: Weixing Wang, Zhonggao Wu, Guole Qi, Guohai Xie
Institution: Ningbo No. 2 Hospital
Language: English
Subfield: Pathology and Forensic Medicine
Field: Medicine
Domain: Health Sciences
Open Access status: gold
Estimated APC paid: $3,090
OpenAlex ID: W7126228420