CA3透明层CA3刺上苔藓纤维突触的年龄诱导损失。

Neuroscience journal Pub Date : 2013-01-01 Epub Date: 2013-06-24 DOI:10.1155/2013/839535
Bunmi Ojo, Heather Davies, Payam Rezaie, Paul Gabbott, Francis Colyer, Igor Kraev, Michael G Stewart
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引用次数: 13

摘要

老年化与海马体退化和轻度认知能力下降有关。海马CA3透明层亚区(CA3- sl)接收来自齿状回巨大苔藓纤维扣的神经元输入,但相对而言,人们对这种突触连接与衰老的完整性知之甚少。利用连续电子显微镜和无偏体视学,我们研究了年轻成年(4个月)、中年(12个月)和老年(28个月)Wistar大鼠CA3- sl中CA3多刺赘生物上苔藓纤维突触的年龄相关变化。我们的数据显示,虽然CA3体积随着年龄的增长而增加,但与4个月大的动物相比,12个月和28个月大的动物CA3- sl内的突触密度显著减少(40-45%)。我们还提供了初步数据,显示老年CA3神经pil明显充满脂褐素和吞噬酶体阳性,激活小胶质细胞过程,并改变血管周围病理。这些数据表明,CA3-SL的突触密度在衰老过程中显著受损,并伴有潜在的突出的超微结构胶质和微血管变化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Age-Induced Loss of Mossy Fibre Synapses on CA3 Thorns in the CA3 Stratum Lucidum.

Age-Induced Loss of Mossy Fibre Synapses on CA3 Thorns in the CA3 Stratum Lucidum.

Age-Induced Loss of Mossy Fibre Synapses on CA3 Thorns in the CA3 Stratum Lucidum.

Age-Induced Loss of Mossy Fibre Synapses on CA3 Thorns in the CA3 Stratum Lucidum.

Advanced ageing is associated with hippocampal deterioration and mild cognitive decline. The hippocampal subregion CA3 stratum lucidum (CA3-SL) receives neuronal inputs from the giant mossy fibre boutons of the dentate gyrus, but relatively little is known about the integrity of this synaptic connection with ageing. Using serial electron microscopy and unbiased stereology, we examined age-related changes in mossy fibre synapses on CA3 thorny excrescences within the CA3-SL of young adults (4-month-old), middle-aged (12-month-old), and old-aged (28-month-old) Wistar rats. Our data show that while there is an increase in CA3 volume with ageing, there is a significant (40-45%) reduction in synaptic density within the CA3-SL of 12- and 28-month-old animals compared with 4-month-old animals. We also present preliminary data showing that the CA3 neuropil in advanced ageing was conspicuously full of lipofuscin and phagolysosome positive, activated microglial cellular processes, and altered perivascular pathology. These data suggest that synaptic density in the CA3-SL is significantly impaired in ageing, accompanied by underlying prominent ultrastructural glial and microvascular changes.

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