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首页> 外文期刊>Journal of Cerebral Blood Flow and Metabolism: Official Journal of the International Society of Cerebral Blood Flow and Metabolism >Arctic ground squirrel (Spermophilus parryii) hippocampal neurons tolerate prolonged oxygen-glucose deprivation and maintain baseline ERK1/2 and JNK activation despite drastic ATP loss.
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Arctic ground squirrel (Spermophilus parryii) hippocampal neurons tolerate prolonged oxygen-glucose deprivation and maintain baseline ERK1/2 and JNK activation despite drastic ATP loss.

机译:北极松鼠(Spermophilus parryii)海马神经元可耐受长时间的氧葡萄糖剥夺,并维持ATP的急剧减少,但仍维持基线ERK1 / 2和JNK的激活。

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摘要

Oxygen-glucose deprivation (OGD) initiates a cascade of intracellular responses that culminates in cell death in sensitive species. Neurons from Arctic ground squirrels (AGS), a hibernating species, tolerate OGD in vitro and global ischemia in vivo independent of temperature or torpor. Regulation of energy stores and activation of mitogen-activated protein kinase (MAPK) signaling pathways can regulate neuronal survival. We used acute hippocampal slices to investigate the role of ATP stores and extracellular signal-regulated kinase (ERK)1/2 and Jun NH(2)-terminal kinase (JNK) MAPKs in promoting survival. Acute hippocampal slices from AGS tolerated 30 mins of OGD and showed a small but significant increase in cell death with 2 h OGD at 37 degrees C. This tolerance is independent of hibernation state or season. Neurons from AGS survive OGD despite rapid ATP depletion by 3 mins in interbout euthermic AGS and 10 mins in hibernating AGS. Oxygen-glucose deprivation does not induce JNK activation in AGS and baseline ERK1/2 and JNK activation is maintained even after drastic depletion of ATP. Surprisingly, inhibition of ERK1/2 or JNK during OGD had no effect on survival, whereas inhibition of JNK increased cell death during normoxia. Thus, protective mechanisms promoting tolerance to OGD by AGS are downstream from ATP loss and are independent of hibernation state or season.Journal of Cerebral Blood Flow & Metabolism (2008) 28, 1307-1319; doi:10.1038/jcbfm.2008.20; published online 9 April 2008.
机译:氧葡萄糖剥夺(OGD)启动了一系列细胞内反应,最终导致敏感物种的细胞死亡。来自北极松鼠(AGS)的神经元是一种冬眠物种,它们在体外和体内均可耐受OGD,而不受温度或甲苯酚的影响。能量储存的调节和丝裂原激活的蛋白激酶(MAPK)信号通路的激活可以调节神经元的存活。我们使用急性海马切片来研究ATP存储和细胞外信号调节激酶(ERK)1/2和Jun NH(2)-末端激酶(JNK)MAPK在促进存活中的作用。来自AGS的急性海马切片可耐受30分钟的OGD,并在37摄氏度下2 h OGD表现出小而显着的细胞死亡增加。这种耐受性与冬眠状态或季节无关。尽管插补中温AGS中的ATP快速消耗了3分钟,而休眠中的AGS则消耗了10分钟,但AGS的神经元仍能通过OGD存活。氧葡萄糖剥夺不会诱导AGS中的JNK活化,即使在ATP急剧消耗后,基线ERK1 / 2和JNK活化仍得以维持。出乎意料的是,在OGD期间抑制ERK1 / 2或JNK对存活没有影响,而抑制JNK则增加了常氧期间的细胞死亡。因此,促进AGS对OGD的耐受性的保护机制是ATP损失的下游,并且与冬眠状态或季节无关。脑血流与代谢杂志(2008)28,1307-1319; doi:10.1038 / jcbfm.2008.20;在线发布于2008年4月9日。

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