Platinum-loaded Cerium Oxide Capable of Repairing Neuronal Homeostasis for Cerebral Ischemia-Reperfusion Injury Therapy.

Effective neuroprotective agents are required to prevent neurological damage caused by reactive oxygen species (ROS) generated by cerebral ischemia-reperfusion injury (CIRI) following an acute ischemic stroke. Herein, we aimed to develop the neuroprotective agents of cerium oxide loaded with platinum clusters engineered modifications (Pt n -CeO 2 ). The density functional theory (DFT) calculations showed that Pt n -CeO 2 could effectively scavenge ROS, including hydroxyl radicals (·OH) and superoxide anions (·O 2 - ). In addition, Pt n -CeO 2 exhibited the superoxide dismutase- and catalase-like enzyme activities, which is capable of scavenging hydrogen peroxide (H 2 O 2 ). The in-vitro studies showed that Pt n -CeO 2 could adjust the restoration of the mitochondrial metabolism to ROS homeostasis, rebalance cytokines, and featured high biocompatibility. The studies in mice cerebral ischemia-reperfusion injury (CIRI) demonstrated that Pt n -CeO 2 could also restore cytokine levels, reduce cysteine aspartate-specific protease (Cleaved Caspase 3) levels, and induce the polarization of microglia to M2-type macrophages, thus inhibiting the inflammatory responses. As a result, Pt n -CeO 2 inhibited the reperfusion-induced neuronal apoptosis, relieved the infarct volume, reduced the neurological severity score, and improved cognitive function. Overall, these findings suggest that the prominent neuroprotective effect of the engineered Pt n -CeO 2 has a significant neuroprotective effect and provides a potential therapeutic alternative for CIRI. This article is protected by copyright. All rights reserved.