de Lacalle S, Insausti R, Gonzalo L M
Departamento de Anatomía, Facultad de Medicina, Universidad de Navarra, 31080 Pamplona.
Rev Med Univ Navarra. 1995 Jan-Mar;39(1):7-13.
The age-related neuronal changes in mnemonic centres were studied in 37 human and 36 rats (Wistar) brains. The age of the brains (without cerebral alterations) was uniformly distributed along the lifespan (16-86 years in humans and 1-36 months in rats). The results showed parallel changes in humans and rats. The neuronal loss oscillated between 3 and 64%, mean 32%. Neuronal death was a continuous process, although there were differences according the centres, for instance, the higher loss was found in the first half of life in the cortex entorhinalis and hippocampus (rat), and the contrary happened in the dorsolateral and basomedial nucleus of amygdala. In other centres, e.g., mamilla body, basal nucleus of Meynert etc. the loss was quite uniform. The modification in nuclear size showed 3 different phases: there was an initial period in which the nuclear area decreased, a second period with an increase and, in the last period, there was a stabilization in humans and a conspicuous decrease in rats. The nuclear enlargement is interpreted as result of the loss of redundance in nervous centres and the stabilization or atrophy as a consequence of loss of the neuronal plasticity.
在37个人类大脑和36个大鼠(Wistar)大脑中研究了记忆中枢与年龄相关的神经元变化。大脑(无脑部病变)的年龄在整个寿命期间均匀分布(人类为16 - 86岁,大鼠为1 - 36个月)。结果显示人类和大鼠存在平行变化。神经元损失在3%至64%之间波动,平均为32%。神经元死亡是一个持续的过程,尽管不同中枢存在差异,例如,内嗅皮质和海马体(大鼠)在生命的前半段损失较高,而杏仁核背外侧核和基底内侧核则相反。在其他中枢,如乳头体、迈内特基底核等,损失相当均匀。核大小的变化呈现3个不同阶段:最初阶段核面积减小,第二阶段增大,最后阶段在人类中趋于稳定,在大鼠中则显著减小。核增大被解释为神经中枢冗余丧失的结果,而稳定或萎缩则是神经元可塑性丧失的后果。