Environmental enrichment enhanced neurogenesis and behavioral recovery after stroke in aged rats

被引:0
|
作者
Yan, Ji [1 ]
Liu, Yan [2 ]
Zheng, Fangda [1 ]
Lv, Dan [3 ]
Jin, Di [4 ]
机构
[1] Shenyang China Med Univ, Dept Lab Med, Peoples Hosp 4, Shenyang, Liaoning, Peoples R China
[2] Shenyang China Med Univ, Dept Neurol, Peoples Hosp 4, Shenyang, Liaoning, Peoples R China
[3] Liaoning Univ Tradit Chinese Med, Dept Lab Med, Affiliated Hosp, Shenyang, Liaoning, Peoples R China
[4] Liaoning Univ Tradit Chinese Med, Dept Acupuncture Neurol, Affiliated Hosp, Shenyang, Liaoning, Peoples R China
来源
AGING-US | 2023年 / 15卷 / 18期
关键词
aging; environmental enrichment; stroke; ET-1; neurogenesis; behavioral recovery; PROMOTES POSTSTROKE NEUROGENESIS; HIPPOCAMPAL REGION; BRAIN; PROLIFERATION; ASTROCYTES; PLASTICITY; GROWTH; CELLS; MODEL; ZONE;
D O I
暂无
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Background and Purpose: Age is identified as a significant prognostic factor for poorer outcome after stroke. However, environmental enrichment (EE) has been reported to promote functional recovery after ischemic stroke. The purpose of this study was to investigate whether environmental enrichment was beneficial to ischemic stroke in aged rats. Methods: Aged rats were randomly assigned as control rats, rats subjected to cerebral ischemia, and rats with cerebral ischemia treated with EE for 30 days. Focal cortical ischemia was induced by intracranial injection of endothelin-1 (ET-1). EE housing began one day after focal ischemia and was maintained for the whole experimental period. We used immunofluorescence staining to analyze the neurogenesis in the subventricular zone (SVZ) and TdT-mediated dUTP-biotin nick-end labeling (TUNEL) assay to evaluate apoptosis. The expression of neuronal nuclei, glial fibrillary acidic protein (GFAP) and Iba-1 around the infarcted area were also measured by double immunohistochemistry. Results: EE enhanced the proliferation of newborn neurons in the SVZ, as well as increased the long-term survival of newborn neurons. EE also exerted effects on inflammation after stroke. Furthermore, EE suppressed apoptosis and improved the motor functions after stroke in the aged rats. Conclusions: EE improved post-stroke recovery on the basis of enhancing neurogenesis in aged rats.
引用
收藏
页码:9453 / 9463
页数:11
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