Morrison J H, Hof P R
Neurobiology of Aging Laboratories, the Fishberg Research Center for Neurobiology, and the Department of Geriatrics and Adult Development, Mount Sinai School of Medicine, New York, NY 10029, USA.
Science. 1997 Oct 17;278(5337):412-9. doi: 10.1126/science.278.5337.412.
Neurodegenerative disorders are characterized by extensive neuron death that leads to functional decline, but the neurobiological correlates of functional decline in normal aging are less well defined. For decades, it has been a commonly held notion that widespread neuron death in the neocortex and hippocampus is an inevitable concomitant of brain aging, but recent quantitative studies suggest that neuron death is restricted in normal aging and unlikely to account for age-related impairment of neocortical and hippocampal functions. In this article, the qualitative and quantitative differences between aging and Alzheimer's disease with respect to neuron loss are discussed, and age-related changes in functional and biochemical attributes of hippocampal circuits that might mediate functional decline in the absence of neuron death are explored. When these data are viewed comprehensively, it appears that the primary neurobiological substrates for functional impairment in aging differ in important ways from those in neurodegenerative disorders such as Alzheimer's disease.
神经退行性疾病的特征是广泛的神经元死亡,导致功能衰退,但正常衰老过程中功能衰退的神经生物学关联尚不太明确。几十年来,人们普遍认为新皮层和海马体中广泛的神经元死亡是大脑衰老不可避免的伴随现象,但最近的定量研究表明,正常衰老过程中神经元死亡是有限的,不太可能导致与年龄相关的新皮层和海马体功能损害。本文讨论了衰老与阿尔茨海默病在神经元丢失方面的定性和定量差异,并探讨了海马回路功能和生化特性中可能在无神经元死亡情况下介导功能衰退的与年龄相关的变化。综合来看这些数据,衰老过程中功能损害的主要神经生物学基础似乎在重要方面与阿尔茨海默病等神经退行性疾病不同。