Bondareff W
Mech Ageing Dev. 1979 Jan;9(1-2):163-71. doi: 10.1016/0047-6374(79)90127-1.
Quantitative analyses of electron micrographs have shown a decrease in the number of synapses in the dentate gyrus of the senescent Fischer-344 rat. The loss of synapses, involving both dendritic spines and shafts and axon terminals of more than one population of presynaptic neurons, did not depend upon the antecedent loss of postsynaptic neurons or their dendrites. These findings suggest that the age-related loss of synapses in the dentate gyrus may depend upon an inability of presynaptic elements to maintain the structural integrity of synapses in senescence. It is proposed that a change in the glycoprotein component of presynaptic plasma membranes resulting from a deficiency in axonal transport mechanisms in the septo-hippocampal pathway may underly this presynaptic malfunction. The resulting partial deafferentation of neurons in the dentate gyrus in senescence appears to be associated with a secondary atrophy of dendrites, which results in a loss of postsynaptic membranes before a loss of postsynaptic neurons can be documented.
对电子显微镜照片的定量分析表明,衰老的Fischer-344大鼠齿状回中的突触数量减少。突触的丧失涉及树突棘、树突干以及不止一类突触前神经元的轴突终末,这并不取决于突触后神经元或其树突先前的丧失。这些发现提示,齿状回中与年龄相关的突触丧失可能取决于突触前成分在衰老过程中无法维持突触的结构完整性。有人提出,海马旁回-海马通路中轴突运输机制的缺陷导致突触前质膜糖蛋白成分的改变,可能是这种突触前功能障碍的基础。衰老过程中齿状回神经元由此产生的部分传入神经阻滞似乎与树突的继发性萎缩有关,这种萎缩导致在记录到突触后神经元丧失之前突触后膜就已丧失。