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在扩散性去极化诱导的细胞毒性水肿期间,神经元的快速超微结构破坏和恢复。

Rapid Neuronal Ultrastructure Disruption and Recovery during Spreading Depolarization-Induced Cytotoxic Edema.

机构信息

Department of Neuroscience and Regenerative Medicine, Medical College of Georgia at Augusta University, Augusta, GA 30912, USA.

Department of Neurosurgery, Medical College of Georgia at Augusta University, Augusta, GA 30912, USA.

出版信息

Cereb Cortex. 2020 Sep 3;30(10):5517-5531. doi: 10.1093/cercor/bhaa134.

Abstract

Two major pathogenic events that cause acute brain damage during neurologic emergencies of stroke, head trauma, and cardiac arrest are spreading depolarizing waves and the associated brain edema that course across the cortex injuring brain cells. Virtually nothing is known about how spreading depolarization (SD)-induced cytotoxic edema evolves at the ultrastructural level immediately after insult and during recovery. In vivo 2-photon imaging followed by quantitative serial section electron microscopy was used to assess synaptic circuit integrity in the neocortex of urethane-anesthetized male and female mice during and after SD evoked by transient bilateral common carotid artery occlusion. SD triggered a rapid fragmentation of dendritic mitochondria. A large increase in the density of synapses on swollen dendritic shafts implies that some dendritic spines were overwhelmed by swelling or merely retracted. The overall synaptic density was unchanged. The postsynaptic dendritic membranes remained attached to axonal boutons, providing a structural basis for the recovery of synaptic circuits. Upon immediate reperfusion, cytotoxic edema mainly subsides as affirmed by a recovery of dendritic ultrastructure. Dendritic recuperation from swelling and reversibility of mitochondrial fragmentation suggests that neurointensive care to improve tissue perfusion should be paralleled by treatments targeting mitochondrial recovery and minimizing the occurrence of SDs.

摘要

在中风、头部创伤和心脏骤停等神经急症中,导致急性脑损伤的两个主要致病事件是传播去极化波和随之发生的穿过皮质损伤脑细胞的相关脑水肿。实际上,人们对在损伤后即刻和恢复期间,扩散去极化(SD)诱导的细胞毒性水肿在超微结构水平上的演变过程几乎一无所知。在雄性和雌性雄性麻醉小鼠的新皮层中,通过双颈动脉短暂闭塞诱发 SD 后,采用双光子活体成像和定量连续切片电子显微镜评估突触回路完整性。SD 触发树突状线粒体迅速碎片化。肿胀的树突干上突触密度的大量增加意味着一些树突棘被肿胀淹没或仅仅回缩。总的突触密度保持不变。突触后树突膜仍然附着在轴突末梢上,为突触回路的恢复提供了结构基础。立即再灌注后,细胞毒性水肿主要消退,这得到树突超微结构恢复的证实。肿胀恢复和线粒体碎片化的可逆性表明,神经强化护理以改善组织灌注应该与靶向线粒体恢复和最小化 SD 发生的治疗同时进行。

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