Isoquercitrin mitigates intestinal ischemia-reperfusion injury by regulating intestinal flora and inhibiting NLRP3 inflammasome activation

作者：Hui Xu, Tianqi He, Suying Chen, Ruirui Shi, Jian Xu, Yu Xing, Dan Shi, Yi-qin Liu, Ben He, Jin‐Hua Gu · 发表于：Redox Biology · 年份：2025 · DOI：10.1016/j.redox.2025.103803 · 被引用次数：16 · 研究领域：Heme Oxygenase-1 and Carbon Monoxide、Genomics, phytochemicals, and oxidative stress、Inflammasome and immune disorders

Intestinal ischemia-reperfusion (II/R) injury, frequently observed in clinical emergencies such as trauma, infection, and transplantation, leads to severe epithelial necrosis, loss of villi, and alarmingly high mortality rates (50 %-90 %), yet current pharmaceutical treatments largely prove ineffective. This study employs network pharmacology alongside in vivo and in vitro experiments to explore the potential of isoquercitrin, a flavonoid abundant in various dietary sources and known for its anti-inflammatory and antioxidant properties, in mitigating intestinal II/R injury. We found that isoquercitrin significantly reinforced the integrity of the intestinal barrier and markedly alleviated damage associated with II/R injury. Additionally, it enhanced the intestinal microbiota structure by promoting microbial diversity and supporting beneficial bacterial populations. According to network pharmacology analyses, isoquercitrin may prevent II/R injury by modulating redox-related pathways and regulating inflammatory responses mediated by the NLRP3 inflammasome. This protective effect is evidenced by reduced levels of reactive oxygen species (ROS) and malondialdehyde (MDA), as well as an increased GSH/GSSG ratio and enhanced superoxide dismutase (SOD) activity. Isoquercitrin also inhibited NLRP3 inflammasome activation and decreased the expression of downstream factors, including Caspase-1, IL-1β, IL-6, and keratinocyte-derived cytokine (KC). The observed effects correlate with enhan...