Patrylo Peter R, Williamson Anne
Department of Physiology, Southern Illinois University School of Medicine Carbondale, IL 62901, USA.
Prog Brain Res. 2007;163:679-96. doi: 10.1016/S0079-6123(07)63037-4.
The central nervous system (CNS) undergoes a variety of anatomic, physiologic, and behavioral changes during aging. One region that has received a great deal of attention is the hippocampal formation due to the increased incidence of impaired spatial learning and memory with age. The hippocampal formation is also highly susceptible to Alzheimer's disease, ischemia/hypoxia, and seizure generation, the three most common aging-related neurological disorders. While data reveal that the dentate gyrus plays a key role in hippocampal function and dysfunction, the majority of electrophysiological studies that have examined the effects of age on the hippocampal formation have focused on CA3 and CA1. We perceive this to be an oversight and consequently will highlight data in this review which demonstrate an age-related disruption in dentate circuitry and function, and propose that these changes contribute to the decline in hippocampal-dependent behavior seen with "normal" aging.
在衰老过程中,中枢神经系统(CNS)会经历各种解剖学、生理学和行为学上的变化。由于随着年龄增长,空间学习和记忆受损的发生率增加,海马结构受到了大量关注。海马结构对阿尔茨海默病、缺血/缺氧和癫痫发作也高度敏感,这三种是最常见的与衰老相关的神经疾病。虽然数据显示齿状回在海马功能和功能障碍中起关键作用,但大多数研究年龄对海马结构影响的电生理研究都集中在CA3和CA1区。我们认为这是一种疏忽,因此将在本综述中强调相关数据,这些数据表明齿状回神经回路和功能存在与年龄相关的破坏,并提出这些变化导致了“正常”衰老过程中出现的海马依赖性行为下降。