Conrad Cheryl D, McLaughlin Katie J, Harman James S, Foltz Cainan, Wieczorek Lindsay, Lightner Elizabeth, Wright Ryan L
Department of Psychology, Arizona State University, Tempe, Arizona 85287-1104, USA.
J Neurosci. 2007 Aug 1;27(31):8278-85. doi: 10.1523/JNEUROSCI.2121-07.2007.
We previously found that chronic stress conditions producing CA3 dendritic retraction and spatial memory deficits make the hippocampus vulnerable to the neurotoxin ibotenic acid (IBO). The purpose of this study was to determine whether exposure to chronic corticosterone (CORT) under conditions that produce CA3 dendritic retraction would enhance CA3 susceptibility to IBO. Male Sprague Dawley rats were chronically treated for 21 d with CORT in drinking water (400 microg/ml), and half were given daily injections of phenytoin (40 mg/kg), an antiepileptic drug that prevents CA3 dendritic retraction. Three days after treatments stopped, IBO was infused into the CA3 region. Conditions producing CA3 dendritic retraction (CORT and vehicle) exacerbated IBO-induced CA3 damage compared with conditions in which CA3 dendritic retraction was not observed (vehicle and vehicle, vehicle and phenytoin, CORT and phenytoin). Additionally, spatial recognition memory was assessed using the Y-maze, revealing that conditions producing CA3 dendritic retraction failed to impair spatial recognition memory. Furthermore, CORT levels in response to a potentially mild stressor (injection and Y-maze exposure) stayed at basal levels and failed to differ among key groups (vehicle and vehicle, CORT and vehicle, CORT and phenytoin), supporting the interpretations that CORT levels were unlikely to have been elevated during IBO infusion and that the neuroprotective actions of phenytoin were not through CORT alterations. These data are the first to show that conditions with prolonged glucocorticoid elevations leading to structural changes in hippocampal dendritic arbors can make the hippocampus vulnerable to neurotoxic challenges. These findings have significance for many disorders with elevated glucocorticoids that include depression, schizophrenia, Alzheimer's disease, and Cushing's disease.
我们之前发现,导致CA3树突回缩和空间记忆缺陷的慢性应激条件会使海马体易受神经毒素鹅膏蕈氨酸(IBO)的影响。本研究的目的是确定在产生CA3树突回缩的条件下暴露于慢性皮质酮(CORT)是否会增强CA3对IBO的易感性。雄性Sprague Dawley大鼠饮用含CORT(400微克/毫升)的水进行21天的慢性治疗,其中一半每天注射苯妥英钠(40毫克/千克),这是一种可防止CA3树突回缩的抗癫痫药物。治疗停止三天后,将IBO注入CA3区域。与未观察到CA3树突回缩的条件(溶剂和溶剂、溶剂和苯妥英钠、CORT和苯妥英钠)相比,产生CA3树突回缩的条件(CORT和溶剂)加剧了IBO诱导的CA3损伤。此外,使用Y迷宫评估空间识别记忆,结果显示产生CA3树突回缩的条件并未损害空间识别记忆。此外,对潜在轻度应激源(注射和Y迷宫暴露)的反应中,CORT水平保持在基础水平,关键组(溶剂和溶剂、CORT和溶剂、CORT和苯妥英钠)之间没有差异,这支持了以下解释:在IBO注入期间CORT水平不太可能升高,并且苯妥英钠的神经保护作用不是通过改变CORT实现的。这些数据首次表明,长期糖皮质激素升高导致海马树突结构变化的条件会使海马体易受神经毒性挑战。这些发现对于许多糖皮质激素升高的疾病具有重要意义,包括抑郁症、精神分裂症、阿尔茨海默病和库欣病。