NIR Driven Pd/Cerium Oxide Nano-Heterojunction for Enhanced Salvaging Sepsis Induced Acute Liver Injury via Reprogramming Redox Homeostasis in Synergy with Inducing Autophagy.

近红外驱动的Pd/氧化铈纳米异质结通过重编程氧化还原稳态与诱导自噬协同作用,增强挽救脓毒症引起的急性肝损伤

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作者:Qin Tao, Qin Lian, Zhao Yang, Chen Yin, Liu Qianyue, Lin Xiaoguang, Lan Yongfeng, Huang Yaohui, Liu Yan, Zhang Ke, Pan Lifan, Li Jiaxiao, Duan Kunpeng, Liang Hao, Yin Mingjing, Fan Guiyang, Liu Lian, Deng Yu, Liao Lin, Su Danke, Gao Ming, Lu Junyu
Sepsis induced acute liver injury (SALI), is a type of acute and severe disease that is generally characterized by producing significant amounts of reactive oxygen species (ROS) in liver tissue, and in response to excessive ROS, producing huge amounts of inflammatory factors by hepatocytes. Considering the crucial role of ROS in SALI, a Pd doped CeO(2) (CP) nano-heterojunction with enhanced ROS scavenging capacity is developed to act as a catalytic nanomedicine for the treatment of SALI. Combining with near infrared (NIR) irradiation, it exhibits excellent scavenging capacity of ROS including hydroxyl radical (•OH), superoxide anion (•O(2) (-)), as well as singlet oxygen ((1)O(2)) for CP. Significantly, it also demonstrates the excellent antioxidant and anti-inflammatory activities for lipopolysaccharides (LPS) stimulated macrophages (RAW264.7), and cecum ligation and puncture (CLP) treated C57BL/6J mice via reducing intracellular ROS levels, decreasing inflammatory factors expression levels, as well as activating Keap1/Nrf-2/HO-1 pathway to reprogram redox homeostasis, induce cellular autophagy, reduce systemic inflammation and promote liver tissue repair, finally achieving the alleviation of SALI. It provides a promising therapeutic strategy of CP+NIR with high efficacy and biosafety for the management of SALI.

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