Department of Surgery, University of Cincinnati, Cincinnati, Ohio.
Division of Critical Care Medicine, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio.
Shock. 2018 Mar;49(3):277-287. doi: 10.1097/SHK.0000000000000984.
Despite therapeutic advances in hemorrhagic shock, mortality from multiple organ failure remains high. AMP-activated protein kinase (AMPK) is involved in cellular energy homeostasis. Two catalytic subunits, α1 and α2, have been identified, with α1 subunit largely expressed in major organs. Here, we hypothesized that genetic deficiency of AMPKα1 worsens hemorrhage-induced multiple organ failure. We also investigated whether treatment with metformin, a clinically used drug for metabolic homeostasis, affords beneficial effects. AMPKα1 wild-type (WT) and knock-out mice (KO) were subjected to hemorrhagic shock by blood withdrawing followed by resuscitation with shed blood and Lactated Ringer's solution and treatment with vehicle or metformin. Mice were sacrificed at 3 h after resuscitation. Compared with vehicle-treated WT animals, KO animals exhibited a more severe hypotension, higher lung and liver injury and neutrophil infiltration, and higher levels of plasma inflammatory cytokines. Metformin treatment ameliorated organ injury and mean arterial blood pressure in both WT and KO mice, without affecting systemic cytokine levels. Furthermore, metformin treatment reduced liver lipid peroxidation and increased levels of complex II cosubstrate FAD and levels of ATP in WT and KO mice. Beneficial effects of metformin were associated with organ-specific nuclear-cytoplasmic shuttling and activation of liver kinase B1 and AMPKα2. Thus, our data suggest that AMPKα1 is an important regulator of hemodynamic stability and organ metabolic recovery during hemorrhagic shock. Our data also suggest that metformin affords beneficial effects, at least in part, independently of AMPKα1 and secondary to AMPKα2 activation, increase of Complex II function and reduction of oxidative stress.
尽管在失血性休克的治疗方面取得了进展,但多器官衰竭导致的死亡率仍然很高。AMP 激活的蛋白激酶(AMPK)参与细胞能量稳态。已经鉴定出两种催化亚基,α1 和 α2,其中 α1 亚基在主要器官中大量表达。在这里,我们假设 AMPKα1 的遗传缺失会加重出血引起的多器官衰竭。我们还研究了二甲双胍(一种用于代谢稳态的临床药物)的治疗是否会产生有益的效果。野生型(WT)和敲除(KO)AMPKα1 小鼠通过抽血引起失血性休克,然后用失血和乳酸林格溶液复苏,并给予载体或二甲双胍治疗。在复苏后 3 小时处死小鼠。与 WT 动物相比,KO 动物表现出更严重的低血压、更高的肺和肝损伤以及中性粒细胞浸润,以及更高水平的血浆炎症细胞因子。二甲双胍治疗改善了 WT 和 KO 小鼠的器官损伤和平均动脉血压,而不影响全身细胞因子水平。此外,二甲双胍治疗降低了 WT 和 KO 小鼠肝脂质过氧化和复合物 II 辅助因子 FAD 的水平,并增加了 ATP 的水平。二甲双胍的有益作用与肝激酶 B1 和 AMPKα2 的器官特异性核质穿梭和激活有关。因此,我们的数据表明 AMPKα1 是失血性休克期间血流动力学稳定和器官代谢恢复的重要调节剂。我们的数据还表明,二甲双胍至少部分通过激活 AMPKα2、增加复合物 II 功能和减少氧化应激发挥有益作用,而与 AMPKα1 无关。