氧化铁纳米颗粒和磁场对大鼠缺血再灌注后海马细胞凋亡和Bax基因表达的影响

Sh Bagheri Tari, Z. K. Koohpar, M. Falahati
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引用次数: 1

摘要

巴宝勒大学医学杂志;20 (2);2018年2月;收稿日期:2017年1月7日,修稿日期:2017年10月22日,收稿日期:2017年12月12日。背景与目的:脑卒中是全球第二大死亡原因。脑卒中后,缺血半暗带的许多神经元发生凋亡。本研究旨在探讨氧化铁纳米颗粒和磁场对大鼠缺血再灌注后细胞凋亡减少的影响。方法:选取体重220 ~ 250g的雄性Wistar大鼠50只,随机分为5组,每组10只:对照组、假手术(缺血再灌注模型)、缺血再灌注+氧化铁纳米颗粒(10mg/kg)组、缺血再灌注+磁场组(1 Tesla, 4 d 20 min)、缺血再灌注+氧化铁纳米颗粒+磁场组。采用腹腔注射。4 d后,取海马进行凋亡诱导(TUNEL法)和Bax基因表达变化(Q-PCR法)的研究。结果:缺血再灌注诱导后4 d内,氧化铁纳米颗粒(7±2)和磁场(12±2)处理的TUNEL+细胞数量较缺血再灌注组(27±5)显著减少(p<0.01)。但与缺血再灌注组(27±5)相比,纳米颗粒与磁场同时处理(23±2.6)天无显著差异。与缺血再灌注模型(5.21±0.73)相比,氧化铁纳米颗粒处理组(2.46±0.22)和磁场暴露组(3.28±0.33)Bax基因表达显著降低(p<0.01)。结论:氧化铁纳米颗粒和磁场是减少缺血再灌注后细胞凋亡的两种有效方法。
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The Role of Iron Oxide Nanoparticles and Magnetic Field on Apoptosis and Bax Gene Expression in Rat Hippocampus after Ischemic Reperfusion
J Babol Univ Med Sci; 20(2); Feb 2018; PP: 42-8 Received: Jan 7 2017, Revised: Oct 22 2017, Accepted: Dec 12 2017. ABSTRACT BACKGROUND AND OBJECTIVE: Stroke is the second leading cause of mortality in the worldwide. After a stroke, many neurons in the ischemic penumbra will undergo apoptosis. The aim of this study was investigation of effects of iron oxide nanoparticles and magnetic field on apoptosis reduction after ischemic reperfusion in rat model. METHODS: In this experimental study, 50 male Wistar rats weighing 220-250g were randomly divided into five groups of 10 rats each: including control, sham (ischemic reperfusion model), ischemic reperfusion+iron oxide nanoparticles (10mg/kg), ischemic reperfusion +magnetic field (1 Tesla, 20 min in 4 days), and ischemic reperfusion+iron oxide nanoparticles and magnetic field groups. Injections were performed intraperitoneally. After Four days, the hippocampi were removed for studying of Apoptosis Induction (by TUNEL technique) and changes in Bax gene expression (by Q-PCR method). FINDINGS: After induction of ischemic reperfusion, TUNEL+ cells number treated with iron oxide nanoparticles (7±2) and or the magnetic field (12±2) had significant decrease (p<0.01) relative to ischemic reperfusion group (27±5) during 4 days. But simultaneous treatment with nanoparticles and magnetic field (23±2.6) did not show significant difference compared to ischemic reperfusion group (27±5) during 4 days. Furthermore Bax gene expression decreased in iron oxide nanoparticles treated group (2.46±0.22) or the magnetic field exposed group (3.28±0.33) significantly (p<0.01)compared to ischemic reperfusion model (5.21±0.73).. CONCLUSION: It seems that iron oxide nanoparticles as well as magnetic field to be two effective methods in decrease of apoptosis after ischemic reperfusion.
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审稿时长
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