Limb Remote Ischemic Postconditioning Improves Glymphatic Dysfunction After Cerebral Ischemia-Reperfusion Injury

被引:2
|
作者
Li, Xiaohong [1 ]
Tan, Xiaoli [1 ]
Zhou, Qian [2 ]
Xie, Zhuoxi [1 ]
Meng, Weiting [1 ]
Pang, Yeyu [1 ]
Huang, Lizhen [1 ]
Ding, Zhihao [1 ]
Hu, Yuanhong [1 ]
Li, Ruhua [1 ]
Huang, Guilan [1 ]
Li, Hao [1 ]
机构
[1] Guilin Med Univ, Dept Neurol, Affiliated Hosp, Guilin 541001, Peoples R China
[2] Guilin Med Univ, Affiliated Hosp 2, Dept Neurol, Guilin 541199, Peoples R China
基金
中国国家自然科学基金;
关键词
aquaporin-4; amyloid-beta; polarization; extracellular volume; ischemic brain edema; BRAIN EDEMA; PATHWAY; STROKE; MECHANISM; THERAPY;
D O I
10.1016/j.neuroscience.2023.04.017
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Background: Delayed neuronal damage can be caused or aggravated after cerebral ischemia-reperfusion (I/R) injury. Recent studies have shown that glymphatic system dysfunction after cerebral ischemia-reperfusion injury is involved in ischemic brain edema and neuroinflammation, thereby regulating cerebral ischemia-reperfusion injury. The aim of this study is to investigate the changes of glymphatic system after cerebral ischemia-reperfusion injury and whether limb remote ischemic postconditioning (LRIP) can improve the function of glymphatic system to protect the brain. Methods: To establish a focal brain I/R injury mouse model, this study utilized the middle cerebral artery occlusion/reperfusion (MCAO/R) method. The present study classified eight-week-old C57BL/6 male mice into three groups. The changes in glymphatic function in different periods of ischemia and reperfusion were analyzed through immunofluorescence, transmission electron microscopy (TEM), and Western-Blot (WB) assays. The contents of the evaluation included cerebrospinal fluid flow, swelling degree of brain tissue, aquaporin-4 (AQP4) expression and polarization, and amyloid-beta (A beta) excretion. Results: In the early stages of cerebral ischemia, cerebrospinal fluid (CSF) flow is disturbed, accompanied by a decrease in AQP4 polarization. The polarity of AQP4 decreased from 12 h to 72 h of reperfusion, the A beta deposition. LRIP can increase the expression of beta-DG and AQP4 polarization, reduce the deposition of A beta, improve the function of the glymphatic system, and reduce the expression of AQP4 to play A protective role in brain. Conclusion: Glymphatic system impaired after cerebral ischemia-reperfusion injury in mice. LRIP may play a neuroprotective role by improving glymphatic function after I/R. (C) 2023 The Author(s). Published by Elsevier Ltd on behalf of IBRO. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
引用
收藏
页码:20 / 30
页数:11
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