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光血栓性大脑中动脉阻塞在小鼠中的应用:一种新的缺血性脑卒中模型。

Photothrombotic Middle Cerebral Artery Occlusion in Mice: A Novel Model of Ischemic Stroke.

机构信息

Neuroscience Institute, National Research Council, 56124 Pisa, Italy

European Laboratory for Non-Linear Spectroscopy, 50019 Sesto Fiorentino, Italy.

出版信息

eNeuro. 2023 Feb 8;10(2). doi: 10.1523/ENEURO.0244-22.2022. Print 2023 Feb.

DOI:10.1523/ENEURO.0244-22.2022
PMID:36650068
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9910575/
Abstract

Stroke is one of the main causes of death and disability worldwide. Over the past decades, several animal models of focal cerebral ischemia have been developed allowing to investigate pathophysiological mechanisms underlying stroke progression. Despite intense preclinical research efforts, the need for noninvasive mouse models of vascular occlusion targeting the middle cerebral artery yet avoiding mechanical intervention is still pressing. Here, by applying the photothrombotic stroke model to the distal branch of the middle cerebral artery, we developed a novel strategy to induce a targeted occlusion of a large blood vessel in mice. This approach induces unilateral damage encompassing most of the dorsal cortex from the motor up to the visual regions 1 week after stroke. Pronounced limb dystonia one day after the damage is partially recovered after one week. Furthermore, we observe the insurgence of blood vessel leakage and edema formation in the peri-infarct area. Finally, this model elicits a notable inflammatory response revealed as a strong increase in astrocyte density and morphologic complexity in the perilesional region of the cortex compared with both other regions of the ipsilesional and contralesional hemispheres, and in sham-operated mice. To conclude, the stroke model we developed induces in mice the light-mediated occlusion of one of the main targets of human ischemic stroke, the middle cerebral artery, free from the limitations of commonly used preclinical models.

摘要

中风是全球范围内主要的死亡和残疾原因之一。在过去的几十年中,已经开发出了几种局灶性脑缺血的动物模型,允许研究中风进展的病理生理机制。尽管进行了大量的临床前研究,但仍迫切需要针对大脑中动脉的非侵入性血管闭塞的小鼠模型,同时避免机械干预。在这里,我们通过将光血栓性中风模型应用于大脑中动脉的远端分支,开发了一种新的策略,以诱导小鼠大血管的靶向闭塞。这种方法诱导了单侧损伤,包括中风后 1 周内从运动区到视觉区的大部分背侧皮质。损伤后一天出现明显的肢体张力障碍,1 周后部分恢复。此外,我们观察到梗塞区周围的血管渗漏和水肿形成。最后,与对侧半球的其他区域以及假手术组相比,该模型在皮质的损伤区域引发了明显的炎症反应,表现为星形胶质细胞密度和形态复杂性的强烈增加。总之,我们开发的中风模型在小鼠中诱导了光介导的大脑中动脉的闭塞,这是人类缺血性中风的主要靶点之一,没有常用临床前模型的局限性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b83c/9910575/88e2f7c74fac/ENEURO.0244-22.2022_f005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b83c/9910575/efff38707209/ENEURO.0244-22.2022_f001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b83c/9910575/eaf48d765557/ENEURO.0244-22.2022_f002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b83c/9910575/38dcdef549ca/ENEURO.0244-22.2022_f003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b83c/9910575/52bb1e14e080/ENEURO.0244-22.2022_f004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b83c/9910575/88e2f7c74fac/ENEURO.0244-22.2022_f005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b83c/9910575/efff38707209/ENEURO.0244-22.2022_f001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b83c/9910575/eaf48d765557/ENEURO.0244-22.2022_f002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b83c/9910575/38dcdef549ca/ENEURO.0244-22.2022_f003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b83c/9910575/52bb1e14e080/ENEURO.0244-22.2022_f004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b83c/9910575/88e2f7c74fac/ENEURO.0244-22.2022_f005.jpg

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