Park Mijeong, Kim Chong-Hyun, Jo Seonmi, Kim Eun Joo, Rhim Hyewhon, Lee C Justin, Kim Jeansok J, Cho Jeiwon
Center for Neuroscience, Korea Institute of Science and Technology, 5 Hwarang-ro 14-gil, Seongbuk-gu, Seoul 136-791, Korea.
Neuroscience Program, Korea University of Science &Technology, 217 Gajeong-ro, Daejeon 34113, Korea.
Sci Rep. 2015 Nov 9;5:16235. doi: 10.1038/srep16235.
Chronic uncontrollable stress has been shown to produce various physiological alterations and impair mnemonic functions in the rodent hippocampus. Impacts on neuronal activities, however, have not been well investigated. The present study examined dorsal CA1 place cells to elucidate the computational changes associated with chronic stress effects on cognitive behaviors. After administering chronic restraint stress (CRS; 6 hours/day for ≥21 consecutive days) to adult male mice, several hippocampal characteristics were examined; i.e., spatial learning, in vitro synaptic plasticity, in vivo place cell recording, and western blot analysis to determine protein levels related to learning and memory. Behaviorally, CRS significantly impeded spatial learning but enhanced non-spatial cue learning on the Morris water maze. Physiologically, CRS reduced long-term potentiation (LTP) of Schaffer collateral/commisural-CA1 pathway, phospho-αCaMKII (alpha Ca2(+)/calmodulin-dependent protein kinase II) level in the hippocampus, and stability of spatial representation and the mean firing rates (FRs) of place cells. Moreover, the local cue-dependency of place fields was increased, and the intra-burst interval (IntraBI) between consecutive spikes within a burst was prolonged following CRS. These results extend the previous findings of stress impairing LTP and spatial learning to CRS modifying physical properties of spiking in place cells that contribute to changes in navigation and synaptic plasticity.
慢性不可控应激已被证明会在啮齿动物海马体中产生各种生理改变并损害记忆功能。然而,对神经元活动的影响尚未得到充分研究。本研究检测了背侧CA1区位置细胞,以阐明与慢性应激对认知行为影响相关的计算变化。对成年雄性小鼠施加慢性束缚应激(CRS;每天6小时,连续≥21天)后,检测了几个海马体特征,即空间学习、体外突触可塑性、体内位置细胞记录以及蛋白质印迹分析,以确定与学习和记忆相关的蛋白质水平。行为学上,CRS显著阻碍了空间学习,但增强了在莫里斯水迷宫上的非空间线索学习。生理学上,CRS降低了谢弗侧支/连合-CA1通路的长时程增强(LTP)、海马体中磷酸化αCaMKII(α钙调蛋白依赖性蛋白激酶II)水平以及空间表征的稳定性和位置细胞的平均放电率(FRs)。此外,CRS后位置野的局部线索依赖性增加,并且一个爆发内连续尖峰之间的爆发内间隔(IntraBI)延长。这些结果将先前关于应激损害LTP和空间学习的发现扩展到CRS改变位置细胞中尖峰的物理特性,这有助于导航和突触可塑性的变化。