Neuritin-overexpressing transgenic mice demonstrate enhanced neuroregeneration capacity and improved spatial learning and memory recovery after ischemia-reperfusion injury
文献类型： 外文期刊
作者： Wan, Kexing 1 ; Mao, Fuxiu 1 ; Li, Qiongqiong 1 ; Wang, Limin 2 ; Wei, Zhiguo 3 ; Wang, Ping 4 ; Liao, Xinhua 5 ; Xu, Men 1 ;
作者机构： 1.Shihezi Univ, Coll Med, Dept Biochem, Shihezi 832000, Xinjiang, Peoples R China
2.Xinjiang Acad Agr & Reclamat Sci, State Key Lab Sheep Genet Improvement & Hlth Prod, Shihezi 832000, Xinjiang, Peoples R China
3.Henan Univ Sci & Technol, Coll Anim Sci & Technol, Luoyang 471023, Henan, Peoples R China
4.Henan Univ Sci & Technol, Coll Anim Food & Bioengn, Luoyang 471023, Henan, Peoples R China
5.Shihezi Univ, Affiliated Hosp 1, Med Coll, Shihezi 832000, Xinjiang, Peoples R China
关键词： transient global ischemia; transgenic mice; neuritin; nerve injury and repair
期刊名称：AGING-US （ 影响因子：5.682； 五年影响因子：6.38 ）
ISSN： 1945-4589
年卷期： 2021 年 13 卷 2 期
页码：
收录情况： SCI
摘要： Acute ischemia-reperfusion (IR)-induced brain injury is further exacerbated by a series of slower secondary pathogenic events, including delayed apoptosis due to neurotrophic factor deficiency. Neuritin, a neurotrophic factor regulating nervous system development and plasticity, is a potential therapeutic target for treatment of IR injury. In this study, Neuritin-overexpressing transgenic (Tg) mice were produced by pronuclear injection and offspring with high overexpression used to generate a line with stable inheritance for testing the neuroprotective capacity of Neuritin against transient global ischemia (TGI). Compared to wild-type mice, transgenic mice demonstrated reduced degradation of the DNA repair factor poly [ADP-ribose] polymerase 1 (PARP 1) in the hippocampus, indicating decreased hippocampal apoptosis rate, and a greater number of surviving hippocampal neurons during the first week post-TGI. In addition, Tg mice showed increased expression of the regeneration markers NF-200, synaptophysin, and GAP-43, and improved recovery of spatial learning and memory. Our findings exhibited that the window of opportunity of neural recovery in Neuritin transgenic mice group had a tendency to move ahead after TGI, which indicated that Neuritin can be used as a potential new therapeutic strategy for improving the outcome of cerebral ischemia injury.
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