Nanomedicine · 2019 · 30 citations · 36 references
Life SciencesBiochemistryPharmacologyApoptosisInflammationNanomaterialsHepatic ToxicityNanocarriers For TherapeuticsNanomedicineOxidative Damage To BiomoleculesOxidative Stress In InflammationReactive Oxygen SpeciesAcute Hepatic FailureAnti-inflammatory ActivityAnti-inflammatory ResponseInflammatory Liver InjuryLiver Injury ModelsNanoparticle ToxicityOxidative Stress In Liver InjuryReactive Oxygen Species Injury
Aim: To explore the potential therapeutic effect of yttrium oxide nanoparticles (Y2O3 NPs) on fulminant hepatic failure. Materials & methods: RAW264.7 cells and a lipopolysaccharide/D-galactosamine-induced hepatic failure murine model were used to assess the effects of Y2O3 NPs. Results: Y2O3 NPs exhibited anti-inflammatory activity by scavenging cellular reactive oxygen species and dampening reactive oxygen species-mediated NF-κB activation in vitro. A single intraperitoneal administration of Y2O3 NPs (30 mg/kg) enhanced hepatic antioxidant status and reduced oxidative stress and inflammatory response in lipopolysaccharide/galactosamine-induced mice. Y2O3 NPs also attenuated hepatic NF-κB activation, cell apoptosis and liver injury. Conclusion: Y2O3 NP administration could be used as a novel therapeutic strategy for treating fulminant hepatic failure and oxidative stress-related diseases.
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Namrata Singh, Mohammed Azharuddin Savanur, Shubhi Srivastava et al. · Angewandte Chemie International Edition · 2017 · 641 citations
Ali Keshavarzian, Ashkan Farhadi, Christopher B. Forsyth et al. · Journal of Hepatology · 2008 · 350 citations · Full text
Pharmacy, Pathobiology, Toxicology +17