溃疡性结肠炎
材料科学
氧化应激
失调
碳化
碳纤维
抗氧化剂
肠道菌群
结肠炎
炎症
活性氧
促炎细胞因子
免疫学
炎症性肠病
药理学
微生物学
化学
治疗效果
发病机制
氧化损伤
氧化磷酸化
炎症性肠病
病态的
炎症反应
细胞
细菌
作者
Xiaozhuo Chen,Xi Luo,Meng Xiao,Xirui Chen,Lijiao Wu,You Yu,Jinming Zhang
标识
DOI:10.1021/acsami.5c14857
摘要
Ulcerative colitis (UC) management remains challenging due to limitations of conventional therapies in disrupting the pathological cycle of ROS overproduction and gut microbiota dysbiosis. Inspired by traditional “carbonized herbs,” this study developed Cimicifugae rhizome-derived carbon dots (CR-CDs) by one-step pyrolysis. CR-CDs exhibited robust multienzyme mimetic (SOD/CAT-like) activity, effectively scavenging ROS and suppressing the LPS-stimulated inflammatory response in vitro. In dextran sulfate sodium (DSS)-induced murine colitis, orally administered CR-CDs accumulated preferentially in inflamed colon tissue and targeted macrophages. Treatment significantly alleviated UC symptoms and histological damage while restoring tight junction proteins and improving the Nrf2/HO-1 antioxidant signaling. Additionally, CR-CDs rebalanced gut microbiota composition, suppressing the pathogenic Aeromonas hydrophila and enriching beneficial Rikenellaceae/Muribaculaceae. By integrating traditional carbonization wisdom with nanotechnology, CR-CDs present a dual-functional therapeutic platform addressing both oxidative stress and microbial dysbiosis in UC, with significant potential for clinical translation.
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