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Mild hypothermia pretreatment protects against liver ischemia reperfusion injury via the PI3K/AKT/FOXO3a pathway

机译:温和的体温过低预处理通过PI3K / AKT / Foxo3a途径免受肝脏缺血再灌注损伤

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Mild hypothermia is known to protect against ischemia and reperfusion (IR) injury. The exact mechanisms of the protection are not fully understood. Forkhead box O3 (FOXO3a) has been defined as a critical mediator in cellular processes, including oxidative stress, apoptosis, inflammation, cell death and DNA repair; however, the protection function in mild hypothermia has not been reported previously. The current study was designed to investigate the function of phosphoinositide 3-kinase (PI3K)/protein kinase B (AKT)/FOXO3a pathway in pretreatment with mild hypothermia during IR injury. Additionally, PI3K/AKT/FOXO3a signaling was inhibited using Ly294002 and the effect on the protective function of mild hypothermia pretreatment was evaluated. Furthermore, the apoptotic and inflammatory response induced by the IR injury was evaluated. Liver IR injury induced a significant increase in the level of apoptosis and inflammatory responses. However, pretreatment with mild hypothermia increased phospho (p)-AKT and p-FOXO3a following IR injury, and significantly reduced apoptosis and inflammatory cytokines release. However, inhibiting p-AKT and p-FOXO3a using Ly294002 suppressed the liver protection produced by mild hypothermia. In conclusion, these findings indicated that mild hypothermia pretreatment exhibited liver protective effects against IR injury associated with suppressing inflammatory cytokine release and apoptosis via the PI3K/AKT/FOXO3a pathway.
机译:众所周知,轻度体温过低,可防止缺血和再灌注(IR)损伤。保护的确切机制不完全理解。 FORKHEAD盒O3(FOXO3A)被定义为细胞过程中的临界介体,包括氧化应激,细胞凋亡,炎症,细胞死亡和DNA修复;然而,先前尚未报告轻度体温过低的保护功能。目前的研究旨在探讨磷酸阳性3-激酶(PI3K)/蛋白激酶B(AKT)/ FoxO3A途径在IR损伤期间用温和体温过低的预处理中的函数。另外,使用LY294002抑制了PI3K / AKT / FOXO3A信号,评价了对轻度体温过低预处理的保护功能的影响。此外,评价IR损伤诱导的凋亡和炎症反应。肝红外损伤诱导凋亡水平和炎症反应的显着增加。然而,用温和的体温过低的预处理增加了IR损伤后磷酸(P)-aKT和P-FoxO3a,并且显着降低了凋亡和炎症细胞因子释放。然而,抑制使用LY294002的P-AKT和P-FOXO3A抑制了通过低温产生的肝脏保护。总之,这些发现表明,轻度体温过低预处理表现出与抑制炎症细胞因子释放和通过PI3K / AKT / FoxO3A途径相关的肝脏保护作用。

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