Department of Psychological and Brain Sciences, Johns Hopkins University, Baltimore, MD, USA.
Department of Neuroscience and Zanvyl Krieger Mind/Brain Institute, Johns Hopkins University, Baltimore, MD, USA.
Neurobiol Aging. 2019 Apr;76:151-161. doi: 10.1016/j.neurobiolaging.2018.12.015. Epub 2019 Jan 8.
Similar to elderly humans, aged outbred Long-Evans rats exhibit individual differences in memory abilities, including a subset of aged rats that maintain memory function on par with young adults. Such individuals provide a basis for investigating mechanisms of resilience to age-related decline. The present study examined hippocampal gene expression in young adults and aged rats with preserved memory function under behavioral task conditions well established for assessing information processing central to the formation of episodic memory. Although behavioral measures and hippocampal gene induction associated with neural activity and synaptic plasticity were similar across age groups, a marker for inhibitory interneuron function in the hippocampal formation was distinctively increased only in aged rats but not in young adults. Because heightened hippocampal neural activity is associated with age-related memory impairment across species, including rats, monkeys, and humans, this finding may represent an adaptive homeostatic adjustment necessary to maintain neural plasticity and memory function in aging.
类似于老年人类,衰老的远交系 Long-Evans 大鼠表现出记忆能力的个体差异,包括一部分衰老的大鼠保持与年轻人相当的记忆功能。这些个体为研究对与年龄相关的衰退的弹性机制提供了基础。本研究在行为任务条件下检查了年轻成年人和具有保存记忆功能的衰老大鼠的海马基因表达,这些行为任务条件是为评估对形成情景记忆至关重要的信息处理而建立的。尽管行为测量和与神经活动和突触可塑性相关的海马基因诱导在不同年龄组之间相似,但海马结构中抑制性中间神经元功能的标志物仅在衰老大鼠中而非在年轻成年人中显著增加。因为在包括大鼠、猴子和人类在内的各种物种中,增强的海马神经活动与与年龄相关的记忆障碍有关,所以这一发现可能代表了一种适应性的平衡调整,这种调整对于维持衰老过程中的神经可塑性和记忆功能是必要的。