脑梗死后微血管及血管周围间隙的超微结构变化

O. Voloshanska, S. I. Tertyshnyi
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Objective – to investigate ultrastructural changes in the vessels of the brain and perivascular space in experimental ischemic heart attack. Methods. Experimental cerebral infarction was reproduced on 15 white Wistar rats by injection of a suspension of barium sulfate in sterile saline in a ratio of 1: 3 in the amount of 0.1 -0.3 ml. Three animals formed a control group. The material was collected in terms of: up to 3, 9, 12 days and more than 12 days from the beginning of the experimental action, followed by standard processing of the material for electron microscopy. Results. In the early stages of ischemic brain damage perivascular edema, destructive changes of capillaries with destruction of basement membranes are registered. Some microvessels undergo irreversible changes with deformation of the vascular lumen, pyknosis and lysis of endothelial nuclei, destruction and vacuolation of cytoplasmic structures, microvacuolation and edema of mitochondria with partial destruction of cristae and enlightenment of the mitochondrial matrix. In the endothelium with signs of coagulation processes in the cytoplasm and nucleus, changes in cell contacts were observed. Structural changes of vessels are combined with changes of perivascular processes of astrocytes. On days 9 and 12, the structure of the endothelium, perivascular astrocytes, and intercellular contacts are restored. Hyperplasia of intracytoplasmic structures, increase in mitochondria and length of cytoplasmic network are noted. In the cells of the perivascular environment and in the cytoplasm of pericytes a significant number of phagolysosomes is detected, in the long term in the perifocal areas of irreversible ischemic changes around the vessels is reparative astrogliosis. Conclusion. Ultrastructural changes of the microcirculatory part in the perifocal areas of ischemic lesions within 3 days are characterized by perivascular edema and destructive changes in the endothelium of capillaries and pericytes, damage to basement membranes, changes in cell contacts. After 9-12 days in the endothelium, the processes of intracellular regeneration increase, the ultrastructure of intercellular contacts is restored. 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引用次数: 0

摘要

背景。缺血性中风是仅次于冠心病的第二大常见死亡原因,也是全世界最常见的致残原因。近年来卒中的基础研究主要关注神经血管阻滞的功能障碍和适应机制,包括血脑屏障结构、小胶质细胞、神经元和基底膜的细胞外基质。近年来,孤立的研究一直致力于缺血性脑损伤的形态学问题,特别是脑的超微结构。同时,只有形态学研究才能揭示细胞结构对各种不利因素影响的响应特性。目的:探讨实验性缺血性心脏病发作时脑血管及血管周围空间的超微结构变化。方法。将硫酸钡混悬液按1:3的比例注射到无菌生理盐水中,0.1 ~ 0.3 ml,复制15只白色Wistar大鼠实验性脑梗死,3只为对照组。收集时间分别为:实验开始后3天、9天、12天和12天以上,然后对材料进行标准处理,用于电镜观察。结果。在缺血性脑损伤血管周围水肿的早期阶段,毛细血管的破坏性变化与基底膜的破坏被记录。一些微血管发生不可逆的变化,血管腔变形,内皮细胞核固缩和溶解,细胞质结构破坏和空泡化,线粒体微空泡化和水肿,嵴部分破坏和线粒体基质启蒙。在内皮细胞中,细胞质和细胞核有凝血过程的迹象,观察到细胞接触的变化。血管的结构改变与星形胶质细胞血管周围突的改变相结合。在第9天和第12天,内皮、血管周围星形胶质细胞和细胞间接触的结构恢复。胞浆内结构增生,线粒体增多,细胞质网络变长。在血管周围环境的细胞和周细胞的细胞质中检测到大量的吞噬溶酶体,长期在血管周围的焦周区域发生不可逆的缺血性变化是修复性星形胶质细胞增生。结论。缺血性病变病灶周围微循环部位3天内超微结构变化表现为血管周围水肿、毛细血管内皮和周细胞内皮破坏改变、基底膜损伤、细胞接触改变。在内皮中培养9 ~ 12 d后,细胞内再生过程增强,细胞间接触的超微结构得到恢复。在血管周围环境的细胞和周细胞的细胞质中记录了大量的吞噬溶酶体,在血管周围不可逆的缺血性变化的焦周区域检测到修复性星形胶质细胞形成。
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Ultrastructural changes in the microvessels and perivascular space in cerebral infarction in the experiment
Background. Ischemic stroke is the second most common cause of death after coronary heart disease and the most common cause of disability worldwide. Much of the recent basic research on stroke is concerned with the mechanisms underlying the dysfunction and adaptation of the neurovascular block, which includes the blood-brain barrier structures, microglia, neurons, and the extracellular matrix of the basement membrane. Isolated studies of recent years have been devoted to the issues of morphology and in particular the ultrastructure of the brain in ischemic injury. Meanwhile, only morphological studies can reveal the peculiarities of the response of cellular structures to the influence of various adverse factors. Objective – to investigate ultrastructural changes in the vessels of the brain and perivascular space in experimental ischemic heart attack. Methods. Experimental cerebral infarction was reproduced on 15 white Wistar rats by injection of a suspension of barium sulfate in sterile saline in a ratio of 1: 3 in the amount of 0.1 -0.3 ml. Three animals formed a control group. The material was collected in terms of: up to 3, 9, 12 days and more than 12 days from the beginning of the experimental action, followed by standard processing of the material for electron microscopy. Results. In the early stages of ischemic brain damage perivascular edema, destructive changes of capillaries with destruction of basement membranes are registered. Some microvessels undergo irreversible changes with deformation of the vascular lumen, pyknosis and lysis of endothelial nuclei, destruction and vacuolation of cytoplasmic structures, microvacuolation and edema of mitochondria with partial destruction of cristae and enlightenment of the mitochondrial matrix. In the endothelium with signs of coagulation processes in the cytoplasm and nucleus, changes in cell contacts were observed. Structural changes of vessels are combined with changes of perivascular processes of astrocytes. On days 9 and 12, the structure of the endothelium, perivascular astrocytes, and intercellular contacts are restored. Hyperplasia of intracytoplasmic structures, increase in mitochondria and length of cytoplasmic network are noted. In the cells of the perivascular environment and in the cytoplasm of pericytes a significant number of phagolysosomes is detected, in the long term in the perifocal areas of irreversible ischemic changes around the vessels is reparative astrogliosis. Conclusion. Ultrastructural changes of the microcirculatory part in the perifocal areas of ischemic lesions within 3 days are characterized by perivascular edema and destructive changes in the endothelium of capillaries and pericytes, damage to basement membranes, changes in cell contacts. After 9-12 days in the endothelium, the processes of intracellular regeneration increase, the ultrastructure of intercellular contacts is restored. A significant number of phagolysosomes is registered in the cells of the perivascular environment and in the cytoplasm of pericytes, and reparative astrogliosis is detected in the perifocal areas of irreversible ischemic changes around the vessels.
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