Molecular and Clinical Pharmacology Program, Institute of Biomedical Sciences, University of Chile, Santiago-7, Chile.
Free Radic Res. 2010 Aug;44(8):854-63. doi: 10.3109/10715762.2010.485995.
N-3 polyunsaturated fatty acids (n-3 PUFA) affect inflammatory processes. This study evaluated the effects of dietary supplementation with fish oil on hepatic ischemia-reperfusion (IR) injury in the rat. Parameters of liver injury (serum transaminases and histology) and oxidative stress (serum 8-isoprostanes and hepatic GSH and GSSG), were correlated with NF-kappaB DNA binding and FA composition and inflammatory cytokine release. N-3 PUFA supplementation significantly increased liver n-3 PUFA content and decreased n-6/n-3 PUFA ratios. IR significantly modified liver histology and enhanced serum transaminases, 8-isoprotanes and inflammatory cytokines, with net reduction in liver GSH levels and net increment in those of GSSG. Early increase (3 h) and late reduction (20 h) in NF-kappaB activity was induced. All IR-induced changes were normalized by n-3 PUFA supplementation. In conclusion, prevention of liver IR-injury was achieved by n-3 PUFA supplementation, with suppression of oxidative stress and recovery of pro-inflammatory cytokine homeostasis and NF-kappaB functionality lost during IR.
n-3 多不饱和脂肪酸(n-3 PUFA)影响炎症过程。本研究评估了鱼油饮食补充对大鼠肝缺血再灌注(IR)损伤的影响。肝损伤参数(血清转氨酶和组织学)和氧化应激(血清 8-异前列腺素和肝 GSH 和 GSSG)与 NF-κB DNA 结合和 FA 组成以及炎症细胞因子释放相关。n-3 PUFA 补充显著增加了肝脏 n-3 PUFA 含量,降低了 n-6/n-3 PUFA 比值。IR 显著改变了肝脏组织学,增加了血清转氨酶、8-异前列腺素和炎症细胞因子,导致肝 GSH 水平降低,GSSG 水平升高。诱导了 NF-κB 活性的早期增加(3 h)和晚期减少(20 h)。n-3 PUFA 补充可使所有 IR 诱导的变化正常化。总之,n-3 PUFA 补充可预防肝 IR 损伤,抑制氧化应激,恢复在 IR 期间丢失的促炎细胞因子平衡和 NF-κB 功能。