中国神经再生研究(英文版) ›› 2022, Vol. 17 ›› Issue (4): 832-837.doi: 10.4103/1673-5374.322470

• 原著:脑损伤修复保护与再生 • 上一篇    下一篇

颈总动脉注射荧光微球致小鼠多发性脑梗死的组织学表现

  

  • 出版日期:2022-04-15 发布日期:2021-10-18

Histochemistry of microinfarcts in the mouse brain after injection of fluorescent microspheres into the common carotid artery

Yi Shen1, #, Ming-Jiang Yao2, 3, #, Yu-Xin Su1, Dong-Sheng Xu1, Jia Wang1, Guang-Rui Wang2, 3, Jing-Jing Cui1, Jian-Liang Zhang1, Wan-Zhu Bai1, *   

  1. 1Institute of Acupuncture and Moxibustion, China Academy of Chinese Medical Sciences, Beijing, China; 2Institute of Basic Medical Sciences, Xiyuan Hospital of China Academy of Chinese Medical Sciences, Beijing, China; 3Beijing Key Laboratory of Pharmacology of Chinese Materia Medica, Beijing, China
  • Online:2022-04-15 Published:2021-10-18
  • Contact: Wan-Zhu Bai, PhD, wanzhubaisy@hotmail.com.
  • Supported by:
    This study was supported by the Project of National Key R&D Program of China, No. 2019YFC1709103 (to WZB); and the National Natural Science Foundation of China, Nos. 81774211 (to WZB), 81873040 (to MJY), 81774432 (to JJC), 81801561 (to DSX), 82004492 (to JW).

摘要:

荧光微球颈总动脉注射建立小鼠多发性脑梗死模型是近年来新出现的一种脑缺血动物模型。为研究这种模型的有效性,实验经颈总动脉中注射直径为45-53 µm的荧光微球,建立了小鼠脑梗死模型。(1)6h后,荧光立体显微镜可直接从大脑表面和切片观察到荧光微球,且其主要分布与注射侧的大脑皮质、纹状体和海马,且在在滞留微球后区域可见微梗死;(2)继而使用荧光组织化学及免疫组化检查与微梗死相关的血管、神经元和神经胶质细胞的变化,见微梗死区域,微球的滞留可引起血管损伤,神经元变性以及星形胶质细胞和小胶质细胞激活;(3)这些组织病理学变化表明,模型有效模拟了引起多灶性微梗死中多种细胞的变化,提示该模型可作为研究缺血性脑卒中发病机制和评价其治疗干预的有效工具。实验于2021年3月16日经中国中医科学院针灸研究所动物伦理委员会批准(批准号D2021-03-16-1)。

https://orcid.org/0000-0001-6285-7788 (Wan-Zhu Bai)

关键词: 荧光微球, 微梗死, 卒中, 颈总动脉, 组织化学, 神经血管单位, 血脑屏障, 神经元

Abstract: The mouse model of multiple cerebral infarctions, established by injecting fluorescent microspheres into the common carotid artery, is a recent development in animal models of cerebral ischemia. To investigate its effectiveness, mouse models of cerebral infarction were created by injecting fluorescent microspheres, 45–53 µm in diameter, into the common carotid artery. Six hours after modeling, fluorescent microspheres were observed directly through a fluorescence stereomicroscope, both on the brain surface and in brain sections. Changes in blood vessels, neurons and glial cells associated with microinfarcts were examined using fluorescence histochemistry and immunohistochemistry. The microspheres were distributed mainly in the cerebral cortex, striatum and hippocampus ipsilateral to the side of injection. Microinfarcts were found in the brain regions where the fluorescent microspheres were present. Here the lodged microspheres induced vascular and neuronal injury and the activation of astroglia and microglia. These histopathological changes indicate that this animal model of multiple cerebral infarctions effectively simulates the changes of various cell types observed in multifocal microinfarcts. This model is an effective, additional tool to study the pathogenesis of ischemic stroke and could be used to evaluate therapeutic interventions. This study was approved by the Animal Ethics Committee of the Institute of Acupuncture and Moxibustion, China Academy of Chinese Medical Sciences (approval No. D2021-03-16-1) on March 16, 2021.

Key words: astrocytes, blood-brain barrier, common carotid artery, fluorescent microsphere, histochemistry, ischemia, microglia, microinfarcts, neuron, neurovascular unit, stroke

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