Article Summary
田士来,康军林,徐小峰,郑茂华,杨 刚.紫檀芪对小鼠缺血性脑损伤后脑水肿期神经细胞凋亡的影响[J].现代生物医学进展英文版,2024,(10):1813-1817.
紫檀芪对小鼠缺血性脑损伤后脑水肿期神经细胞凋亡的影响
The Effect of Pterostilbene on Neuronal Apoptosis during Brain Edema after Ischemia Reperfusion Injury in Mice
Received:January 16, 2024  Revised:February 11, 2024
DOI:10.13241/j.cnki.pmb.2024.10.003
中文关键词: 紫檀芪  脑缺血再灌注损伤  细胞凋亡  小鼠
英文关键词: Pterostilbene  Ischemia reperfusion injury  Cell apoptosis  Mouse
基金项目:甘肃省青年科技基金项目(23JRRA1611);兰州大学第一医院院内基金项目(ldyyyn2020-48)
Author NameAffiliationE-mail
田士来 兰州大学第一医院神经外科 甘肃 兰州 730000 tsl15944361572@163.com 
康军林 兰州大学第一医院神经外科 甘肃 兰州 730000  
徐小峰 兰州大学第一医院神经外科 甘肃 兰州 730000  
郑茂华 兰州大学第一医院神经外科 甘肃 兰州 730000  
杨 刚 兰州大学第一医院神经外科 甘肃 兰州 730000  
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中文摘要:
      摘要 目的:探索紫檀芪(PTE)对小鼠缺血性脑损伤后脑水肿期神经细胞凋亡的影响。方法:将实验小鼠分为3组即假手术组(sham组)、脑缺血再灌注损伤组(IR组)和紫檀芪治疗组(PTE+IR组),其中PTE于造模前连续5天每天腹腔给药(5 mg/kg)1次;然后于造模后3 d进行脑组织TTC染色并计算脑梗死体积比;于造模后2 h、12 h和1、2、4、6、8、10、12及14 d进行小鼠神经行为学评分;使用TUNEL试剂盒于造模后3、7和14 d检测缺血半暗带和海马的凋亡神经细胞。结果:PTE可减轻脑梗死体积、改善神经行为学评分以及抑制缺血半暗带和海马的神经细胞凋亡。结论:PTE在小鼠缺血性脑损伤后脑水肿期具有明确的神经保护作用,其机制与抑制细胞凋亡有关。
英文摘要:
      ABSTRACT Objective: To explore the effect of pterostilbene on neuronal apoptosis during brain edema after ischemia reperfusion injury in mice. Methods: The experimental mice were randomly divided into three groups: sham group, IR group and PTE+IR group. The dose of PTE was injected intraperitoneally with 5 mg/kg once a day for 5 days totally. The cerebral infarct image was stained by TTC and the cerebral infarct volume was measured by Image J after IR 3 d. The neurological behavioral scores were tested after IR1/12, 1/2, 1, 2, 4, 6, 8, 10, 12 and 14 d. The neuronal apoptotic percentage of cerebral ischemic penumbra and ipsilateral hippocampus were detected by TUNEL detection kit after IR3, 7 and 14 d. Results: PTE lowered cerebral infarct volume, improved neurological behavioral scores and inhibited neuronal apoptosis of cerebral ischemic penumbra and ipsilateral hippocampus. Conclusion: PTE presents a continuous neuroprotective effect against ischemia reperfusion during cerebral edema in mice by suppression of cell apoptosis.
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