Robitsek Jonathan, Ratner Marcia H, Stewart Tara, Eichenbaum Howard, Farb David H
Laboratory of Molecular Neurobiology, Department of Pharmacology and Experimental Therapeutics, Boston University School of Medicine, Boston, Massachusetts.
Department of Psychology, Center for Memory and Brain, Boston University, Boston, Massachusetts.
Hippocampus. 2015 Dec;25(12):1541-55. doi: 10.1002/hipo.22474. Epub 2015 Jul 14.
Learning and memory deficits associated with age-related mild cognitive impairment have long been attributed to impaired processing within the hippocampus. Hyperactivity within the hippocampal CA3 region that is associated with aging is mediated in part by a loss of functional inhibitory interneurons and thought to underlie impaired performance in spatial memory tasks, including the abnormal tendency in aged animals to pattern complete spatial representations. Here, we asked whether the spatial firing patterns of simultaneously recorded CA3 and CA1 neurons in young and aged rats could be manipulated pharmacologically to selectively reduce CA3 hyperactivity and thus, according to hypothesis, the associated abnormality in spatial representations. We used chronically implanted high-density tetrodes to record the spatial firing properties of CA3 and CA1 units during animal exploration for food in familiar and novel environments. Aged CA3 place cells have higher firing rates, larger place fields, less spatial information content, and respond less to a change from a familiar to a novel environment than young CA3 cells. We also find that the combination of levetiracetam (LEV) + valproic acid (VPA), previously shown to act as a cognitive enhancer in tests of spatial memory, attenuate CA3 place cell firing rates, reduce place field area, and increase spatial information content in aged but not young adult rats. This is consistent with drug enhancing the specificity of neuronal firing with respect to spatial location. Contrary to expectation, however, LEV + VPA reduces place cell discrimination between novel and familiar environments, i.e., spatial correlations increase, independent of age even though drug enhances performance in cognitive tasks. The results demonstrate that spatial information content, or the number of bits of information encoded per action potential, may be the key correlate for enhancement of spatial memory by LEV + VPA.
长期以来,与年龄相关的轻度认知障碍所导致的学习和记忆缺陷一直被认为是由海马体内部处理功能受损所致。与衰老相关的海马体CA3区域的过度活跃,部分是由功能性抑制性中间神经元的丧失所介导的,并且被认为是空间记忆任务表现受损的基础,包括老年动物在模式完成空间表征方面的异常倾向。在这里,我们探讨是否可以通过药理学手段操纵年轻和老年大鼠同时记录的CA3和CA1神经元的空间放电模式,以选择性地降低CA3的过度活跃,从而根据假设减少空间表征中的相关异常。我们使用长期植入的高密度四极管,在动物于熟悉和新颖环境中寻找食物的过程中,记录CA3和CA1单元的空间放电特性。与年轻的CA3细胞相比,老年CA3位置细胞具有更高的放电率、更大的位置野、更低的空间信息含量,并且对从熟悉环境到新颖环境的变化反应更小。我们还发现,左乙拉西坦(LEV)+丙戊酸(VPA)的组合,先前已证明在空间记忆测试中可作为认知增强剂,可降低老年大鼠而非年轻成年大鼠的CA3位置细胞放电率,减小位置野面积,并增加空间信息含量。这与药物增强神经元放电相对于空间位置的特异性是一致的。然而,与预期相反,LEV + VPA降低了位置细胞在新颖和熟悉环境之间的辨别能力,即空间相关性增加,与年龄无关,尽管药物可提高认知任务的表现。结果表明,空间信息含量,即每个动作电位编码的信息量,可能是LEV + VPA增强空间记忆的关键相关因素。