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- W1201417411 abstract "GTL alone. CONCLUSIONS: High concentrations of UFA, IL-1beta and IL-8 in necrosis fluid relative to NIC fluids supports these to be the potential culprits in necrotic cell death as evidenced by high DNA content in the post-necrotic fluid. The ability of orlistat to reduce serum lipase, NEFA, UFA, LA concentrations in rat serum demonstrates its efficacy as a lipase inhibitor in this model. The high mortality, necrosis, IL-1beta and IL-8 concentrations, distant organ injury in GTL infused rats, and reduction of these with orlistat supports lipolytic generation of UFAs to be the driver of inflammation and necrosis. Therefore, the combined data suggests that lipotoxicity may drive inflammation and necrosis in human acute pancreatitis. Table 1: Human Data" @default.
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- W1201417411 date "2013-05-01" @default.
- W1201417411 modified "2023-10-11" @default.
- W1201417411 title "Sa1351 Neutrophil Gelatinase-Associated Lipocalin: An Early Biomarker for Predicting Acute Kidney Injury in Patients With Acute Pancreatitis" @default.
- W1201417411 doi "https://doi.org/10.1016/s0016-5085(13)60956-7" @default.
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