Department of Psychology, University of Washington, Seattle, WA, 98195, USA.
School of Psychology, Korea University, Seoul, 02841, Republic of Korea.
Mol Psychiatry. 2023 Jul;28(7):2750-2763. doi: 10.1038/s41380-023-01986-4. Epub 2023 Feb 9.
Stressful experiences, both physical and psychological, that are overwhelming (i.e., inescapable and unpredictable), can measurably affect subsequent neuronal properties and cognitive functioning of the hippocampus. At the cellular level, stress has been shown to alter hippocampal synaptic plasticity, spike and local field potential activity, dendritic morphology, neurogenesis, and neurodegeneration. At the behavioral level, stress has been found to impair learning and memory for declarative (or explicit) tasks that are based on cognition, such as verbal recall memory in humans and spatial memory in rodents, while facilitating those that are based on emotion, such as differential fear conditioning in humans and contextual fear conditioning in rodents. These vertically related alterations in the hippocampus, procedurally observed after subjects have undergone stress, are generally believed to be mediated by recurrently elevated circulating hypothalamic-pituitary-adrenal (HPA) axis effector hormones, glucocorticoids, directly acting on hippocampal neurons densely populated with corticosteroid receptors. The main purposes of this review are to (i) provide a synopsis of the neurocognitive effects of stress in a historical context that led to the contemporary HPA axis dogma of basic and translational stress research, (ii) critically reappraise the necessity and sufficiency of the glucocorticoid hypothesis of stress, and (iii) suggest an alternative metaparadigm approach to monitor and manipulate the progression of stress effects at the neural coding level. Real-time analyses can reveal neural activity markers of stress in the hippocampus that can be used to extrapolate neurocognitive effects across a range of stress paradigms (i.e., resolve scaling and dichotomous memory effects issues) and understand individual differences, thereby providing a novel neurophysiological scaffold for advancing future stress research.
身体和心理上的压力体验,无论是压倒性的(即无法逃避和不可预测的),都可以显著影响海马体的后续神经元特性和认知功能。在细胞水平上,压力已被证明会改变海马体的突触可塑性、尖峰和局部场电位活动、树突形态、神经发生和神经退行性变。在行为水平上,压力已被发现会损害基于认知的陈述性(或显性)任务的学习和记忆,例如人类的言语回忆记忆和啮齿动物的空间记忆,同时促进基于情绪的任务,例如人类的差异恐惧条件反射和啮齿动物的情境恐惧条件反射。这些在海马体中垂直相关的改变,在受试者经历压力后程序性地观察到,通常被认为是由反复升高的循环下丘脑-垂体-肾上腺 (HPA) 轴效应激素,糖皮质激素,直接作用于富含皮质甾酮受体的海马神经元介导的。本综述的主要目的是:(i) 在历史背景下概述应激的神经认知效应,这导致了当代 HPA 轴基本和转化应激研究的教条,(ii) 批判性地重新评估应激的糖皮质激素假说的必要性和充分性,以及 (iii) 提出一种替代的元范式方法来监测和操纵神经编码水平的应激效应进展。实时分析可以揭示海马体中应激的神经活动标志物,可用于推断一系列应激范式中的神经认知效应(即解决缩放和二分记忆效应问题)并理解个体差异,从而为推进未来的应激研究提供新的神经生理学支架。