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• W2017607004 abstract "Intracerebral hemorrhage (ICH) is a stroke subtype with significant mortality and morbidity. The role of unconjugated bilirubin (UBR) in ICH brain injury is not well understood. Therefore, we studied the effects of UBR on brain injury markers and inflammation, as well as mechanisms involved therein. We induced ICH in mice by infusion of autologous whole blood with vehicle (dimethyl sulfoxide) or UBR. We found that UBR led to an increase in edema ( P0.05), but a decrease in nitrate/nitrite formation (7.0±0.40 nmol/mg versus 5.2±0.70 nmol/mg protein, P0.05) and no change in protein carbonyls. Unconjugated bilirubin was also associated with an increase in neutrophil infiltration compared with ICH alone, as determined by both immunofluorescence and flow cytometry (36%±3.2% versus 53%±1.3% of CD45 + cells, P0.05). In contrast, we observed reduced perihematomal microglia immunoreactivity in animals receiving UBR ( P0.05). Using in vitro techniques, we show neutrophil activation by UBR and also show that protein kinase C participates in this signaling pathway. Finally, we found that UBR was associated with an increased expression of the leukocyte adhesion molecule intercellular adhesion molecule-1. Our results suggest that UBR possesses complex immune-modulatory and antioxidant effects." @default.
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• W2017607004 date "2010-11-24" @default.
• W2017607004 modified "2023-10-13" @default.
• W2017607004 title "Unconjugated Bilirubin Contributes to Early Inflammation and Edema after Intracerebral Hemorrhage" @default.
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• W2017607004 doi "https://doi.org/10.1038/jcbfm.2010.203" @default.
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