首页> 外文期刊>The Journal of Neuroscience: The Official Journal of the Society for Neuroscience >Loss of presynaptic and postsynaptic structures is accompanied by compensatory increase in action potential-dependent synaptic input to layer V neocortical pyramidal neurons in aged rats.
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Loss of presynaptic and postsynaptic structures is accompanied by compensatory increase in action potential-dependent synaptic input to layer V neocortical pyramidal neurons in aged rats.

机译:突触前和突触后结构的丧失伴随着老年大鼠V层新皮层锥体神经元动作电位依赖性突触输入的补偿性增加。

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摘要

Reduction in both presynaptic and postsynaptic structures in the aging neocortex may significantly affect functional synaptic properties in this area. To directly address this issue, we combined whole-cell patch-clamp recording of spontaneously occurring postsynaptic currents (PSCs) with morphological analysis of layer V pyramidal neurons in the parietal cortex of young adult (1- to 2-month-old) and aged (28- to 37-month-old) BN x F344 F(1) hybrid rats. Analysis of spontaneous PSCs was used to contrast functional properties of basal synaptic input with structural alterations in the dendritic tree of pyramidal neurons and density of terminals in contact with these cells. We observed significant changes in a number of morphological parameters of pyramidal neurons in aged rats. These include smaller cell body size and fewer basal dendritic branches (but not of oblique dendrites and dendritic tufts) and spines. Ultrastructural analysis also revealed a lower density of presynaptic terminals per unit length of postsynaptic membrane of labeled pyramidal neurons in the aged brain. This reduction in both presynaptic and postsynaptic elements was paralleled by a significant decrease in frequency of tetrodotoxin-insensitive miniature (action potential-independent) PSCs (mPSCs). The frequency of excitatory and inhibitory mPSCs was reduced to the same extent. In contrast, no significant change was observed in the frequency of spontaneous PSCs recorded in absence of tetrodotoxin (sPSCs), indicating an increase in action potential-dependent (frequency(sPSCs) - frequency(mPSCs)) input to pyramidal neurons in the aged group. This functional compensation may explain the lack of drastic loss of spontaneous neuronal activity in normal aging.
机译:衰老的新皮层中突触前和突触后结构的减少可能会严重影响该区域的功能性突触特性。为了直接解决这个问题,我们结合了自发发生的突触后电流(PSC)的全细胞膜片钳记录和年轻人(1至2个月大)的顶叶皮质V层锥体神经元的形态分析(28至37个月大)BN x F344 F(1)杂种大鼠。自发性PSC的分析被用来对比基底突触输入的功能特性与锥体神经元树突树中的结构改变以及与这些细胞接触的末端密度。我们观察到老年大鼠锥体神经元的许多形态学参数的显着变化。这些包括较小的细胞体大小和较少的基础树突分支(但不包括斜树突和树突簇)和刺。超微结构分析还显示,老年大脑中标记的锥体神经元的突触后膜每单位长度的突触前末端密度较低。突触前和突触后元件的这种减少与河豚毒素不敏感的微型(独立于动作电位的)PSC(mPSC)的频率显着降低同时发生。兴奋性和抑制性mPSC的频率降低了相同程度。相比之下,在没有河豚毒素(sPSCs)的情况下记录的自发PSC的频率没有观察到显着变化,表明在老年组中输入到锥体神经元的动作电位依赖性(频率(sPSCs-频率(mPSCs))增加) 。这种功能上的补偿可以解释正常衰老中自发性神经元活性的急剧丧失。

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