Neuroglial relationships and structures of interneuronal communication of the white rat sensorimotor cortex layer v after the common carotid artery ligation

L. M. Makar'eva, M. Korzhuk, V. A. Akulinin, S. Stepanov, A. Y. Shoronova, D. Avdeev
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引用次数: 2

Abstract

The aim of research was to study changes in neurons, gliocytes and structures of the interneuronal communication system (dendrites, terminals) of the mature white rat sensorimotor cortex (SMC) layer V after the common carotid artery (CCA) bilateral ligation.Material and methods. Acute/chronic incomplete cerebral ischemia was simulated in white Wistar rats by the CCA bilateral ligation. The brain was fixed by perfusion. A comparative histological, immunohistochemical and morphometric evaluation of the related structures in the norm (n=6), and in 1, 3, 7, 14 and 30 days after the common carotid artery bilateral ligation (n=30) was carried out. Nissl and hematoxylin-eosin stains, immunohistochemical reactions for NSE, MAP-2, p38, GFAP and IBA1 were used. The numerical density of pyramidal neurons, astrocytes, oligodendrocytes, microgliocytes and the relative area of p38-positive material (synapse terminals) were determined. Statistical hypotheses were tested by nonparametric methods using Statistica 8.0 program.Results. CCA bilateral ligation led to the appearance of destructively altered dark, hypochromic, vacuolated neurons and shadow cells in layer V of the SMC. These changes were accompanied by a decreased overall numerical density of pyramidal neurons, hyperhydration of the neuropil (processes of dendrites, astrocytes, and synapses), and a pronounced reaction (hypertrophy, proliferation) of all neuroglial cell types. One day after the CCA bilateral ligation, the appearance of neurons with both reversible and irreversible changes was accompanied by an increase in the layer V relative area of edema-swelling zones in the neuropil of the rat SMC up to 14.5 (10.6– 16.4) %, in control – 7.2 (6.9–7.5) %. The maximum content of destructively altered neurons (25%) was found in the rat SMC layer V one day after ischemia. The total number density of neurons in layer V of the SMC decreased by 27.9% after 30 days (Mann–Whitney U Test; p=0.0001). In the areas of damaged neuron accumulation, the content of astrocytes, microgliocytes, and oligodendrocytes increased. The neuroglial index in the control group was 1.30; it was 1.37 in 3 days, it was 1.50 in 7 days, it was 1.63 in 14 days, and it was 1.30 in 30 days. The maximum increase in the number density of microgliocytes was noted after 1 day (Mann–Whitney U Test; p=0.001), oligodendrocytes – 7 days after CCA ligation (Mann–Whitney U Test; p=0.02). According to the data of immunohistochemical typing of p38, two peaks of the relative area of the terminals were revealed: in the acute period (days 1 and 3) and after 30 days. These quantitative changes were first associated with an increase (on the 1st and 3rd day) and then a decrease in the degree of the neuropil hydration. Negative statistically significant strong correlations were detected in 3 days (R=-0.90) and 7 days (R=-0.70) after CCA ligation. This can be explained by hydropic changes in the terminals (destruction of synapses according to the light type). The total numerical density of neuropil terminals decreased to 102300±19400 (by 35.0%) in 3 days after CCA ligation in layer V of white rats and partially recovered to 135000±27100 (24.4%) after 30 days, compared to the animals of the control (157500±20500 per 1 mm2).Conclusion. Thus, the CCA ligation resulted in destructive and compensatory-restorative changes in the structures of interneuronal communication associated with preservation of a significant part of pyramidal neurons and compensatory reorganization of neuroglial relationships in layer V of white rats.
颈总动脉结扎后大鼠感觉运动皮层v层的神经胶质关系及神经元间通讯结构
本研究旨在研究成熟大鼠双侧颈总动脉结扎后感觉运动皮层(SMC) V层神经元、胶质细胞及神经元间通讯系统(树突、末梢)结构的变化。材料和方法。采用CCA双侧结扎法模拟白Wistar大鼠急性/慢性不完全性脑缺血。脑灌注固定。对正常(n=6)和双侧颈总动脉结扎后1、3、7、14和30天(n=30)相关结构进行比较组织学、免疫组织化学和形态计量学评价。采用尼氏染色和苏木精-伊红染色,对NSE、MAP-2、p38、GFAP和IBA1进行免疫组化反应。测定锥体神经元、星形胶质细胞、少突胶质细胞、小胶质细胞的数量密度和p38阳性物质(突触末端)的相对面积。使用Statistica 8.0程序采用非参数方法对统计假设进行检验。CCA双侧结扎导致SMC V层出现破坏性改变的黑色、低色、空泡化神经元和阴影细胞。这些变化伴随着锥体神经元的总体数值密度下降,神经细胞(树突、星形胶质细胞和突触的过程)的过度水合,以及所有神经胶质细胞类型的明显反应(肥大、增殖)。CCA双侧结扎1天后,出现可逆和不可逆变化的神经元,同时大鼠SMC神经膜水肿肿胀区V层相对面积增加14.5(10.6 - 16.4)%,对照组为7.2(6.9-7.5)%。在缺血后第1天,大鼠SMC第V层的破坏性改变神经元含量最高(25%)。30天后,大鼠神经细胞内第V层神经元总数密度下降27.9% (Mann-Whitney U Test;p = 0.0001)。在受损神经元聚集区,星形胶质细胞、小胶质细胞和少突胶质细胞的含量增加。对照组神经胶质指数为1.30;3天为1.37,7天为1.50,14天为1.63,30天为1.30。小胶质细胞的数量密度在1天后达到最大值(Mann-Whitney U Test;p=0.001),少突胶质细胞- CCA结扎后7天(Mann-Whitney U检验;p = 0.02)。p38免疫组化分型数据显示,急性期(第1、3天)和急性期(第30天)出现两个终末相对面积峰。这些定量变化首先与神经pil水化程度的增加(第1天和第3天)相关,然后降低。CCA结扎后第3天(R=-0.90)和第7天(R=-0.70)出现负统计学意义的强相关。这可以用末端的水力变化来解释(根据光类型破坏突触)。与对照组(157500±20500 / 1 mm2)相比,大鼠V层CCA结扎后3天神经末梢总数值密度下降至102300±19400(下降35.0%),30天后部分恢复至135000±27100(24.4%)。因此,CCA结扎导致大鼠V层神经元间通讯结构的破坏性和代偿性-恢复性变化,这与保存大量锥体神经元和神经胶质关系的代偿性重组有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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