Kreydiyyeh Sawsan Ibrahim, Riman Sarah, Serhan Maya, Kassardjian Ari
Department of Biology, Faculty of Arts & Sciences, American University of Beirut, Beirut, Lebanon.
Prostaglandins Other Lipid Mediat. 2007 Jun;83(4):295-303. doi: 10.1016/j.prostaglandins.2007.02.003. Epub 2007 Feb 17.
The effect of TNF-alpha on liver Na(+)-K(+) ATPase was studied in Sprague-Dawley rats and in HepG2 cells. TNF-alpha was injected intraperitoneally to rats and 4h later the liver was isolated and the activity and protein expression of hepatic Na(+)-K(+) ATPase studied. The cytokine caused a significant down-regulation of the ATPase and a decrease in its activity. This effect disappeared in presence of indomethacin, an inhibitor of COX enzymes, and PGE2 injected to the animals imitated the effect of TNF-alpha. The observed in vivo effects of TNF and PGE2 on the pump appeared again when HepG2 cells were treated with the cytokine or the prostaglandin. The application of different agonist and antagonist to EP receptors showed that the effect of PGE2 is mediated via EP2 receptors. It was concluded that TNF-alpha induces in hepatocytes, PGE2 production which in turn reduces the activity and protein expression of the Na(+)-K(+) ATPase by activating EP2 receptors.
在斯普拉格-道利大鼠和HepG2细胞中研究了肿瘤坏死因子-α(TNF-α)对肝脏钠钾ATP酶的影响。向大鼠腹腔注射TNF-α,4小时后分离肝脏,研究肝脏钠钾ATP酶的活性和蛋白表达。该细胞因子导致ATP酶显著下调及其活性降低。在环氧化酶(COX)酶抑制剂吲哚美辛存在的情况下,这种效应消失,向动物注射前列腺素E2(PGE2)可模拟TNF-α的效应。当用该细胞因子或前列腺素处理HepG2细胞时,观察到的TNF和PGE2对该泵的体内效应再次出现。应用不同的EP受体激动剂和拮抗剂表明,PGE2的作用是通过EP2受体介导的。得出的结论是,TNF-α诱导肝细胞产生PGE2,进而通过激活EP2受体降低钠钾ATP酶的活性和蛋白表达。