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戊四氮致痫幼鼠不同脑区脑损伤研究
引用本文:陈琅,陈巧彬,方琼,娄五斌,高学杰,周俊香.戊四氮致痫幼鼠不同脑区脑损伤研究[J].福建医科大学学报,2014(3):147-150.
作者姓名:陈琅  陈巧彬  方琼  娄五斌  高学杰  周俊香
作者单位:[1]福建医科大学省立临床医学院福建省立医院儿科,福州350001; [2]河南省新乡市医院儿科,新乡453000; [3]福建省妇幼保健院儿科,福州350001; [4]福建省宁德市医院康复科,宁德352000
基金项目:福建省自然基金(2010J01121);福建省医学创新基金(2009-CXB-8)
摘    要:目的:研究S100B蛋白、碱性髓鞘蛋白(MBP)和神经元特异性烯醇酶(NSE)在戊四氮(PTZ)诱导致痫幼鼠海马、额叶、中脑和血清中的动态改变,评鉴癫痫(EP)造成不同脑区的神经损伤。方法雄性SD幼鼠60只,随机分对照组(10只)和实验组(50只)。实验组腹腔注射(IP)PTZ 50 mg/kg 1次,A组IP生理盐水。根据EP发作分级,0~1级9只视为B组,立即取脑;2级以上发作41只,于EP发作后0 h(C=10)、6 h(D=11)、24 h (E=10)、72 h(F=10)断头,分别取下海马、中脑和额叶皮质,断头前抽取躯干血。采用ELISA法检测血清和各脑区S100B和MBP ,采用EIA法检测血清和各脑区 NSE值。结果 EP发作后,海马、额叶和血清S100B蛋白、MBP和NSE均明显高于对照组。海马和额叶的NSE峰值出现在中脑NSE之前。各脑区和血清S100B蛋白皆于EP后24 h达高峰,而MBP于EP后72 h达高峰。结论 EP发作可以造成大脑不同脑区神经元细胞、胶质细胞和神经髓鞘的损伤。

关 键 词:癫痫  戊四氮    磷酸丙酮酸水合酶  S100蛋白质类  髓磷脂碱性蛋白质类  大鼠  Sprague-Dawley

A Study of the Brain Damage of Pentylenetetrazol-Induced Epilepsy Young Rats
CHEN Lang,CHEN Qiaobin,FANG Qiong,LOU Wubin,GAO Xuejie,ZHOU Junxiang.A Study of the Brain Damage of Pentylenetetrazol-Induced Epilepsy Young Rats[J].Journal of Fujian Medical University,2014(3):147-150.
Authors:CHEN Lang  CHEN Qiaobin  FANG Qiong  LOU Wubin  GAO Xuejie  ZHOU Junxiang
Institution:CHEN Lang,CHEN Qiaobin,FANG Qiong,LOU Wubin,GAO Xuejie,ZHOU Junxiang(1. Department of Pediatrics, Fujian Provincial Hospital, Provincial Clinical Medical College of Fujian Medical University, Fuzhou 350001, China; 2. Department of Pediatrics, Henan Xinxiang City HospitaI,Xinxiang 453000, China; 3. Department of Pediatrics, Fujian Maternal and Child Hospital, Fuzhou 350001, China; 4. Department of Rehabilitation, Fujian Ningde Hospital, Ningde 352000, China)
Abstract:Objective By ELISA and EIA evaluated the levels of S100B protein ,myelin basic pro-tein (MBP) and Neuron-specific enolase (NSE) in the serum ,hippocampus ,mesencephalon and frontal cortex in pentylenetetrazol (PTZ) induced epilepsy young rats to study the brain damage after seizure at-tacked . Methods 60 male aged 4~5 weeks young SD rats were divided into control and experimental groups randomly . The control group(A=10) was injected intraperioneally (IP) with the same value of normal saline and the experimental group was IP with PTZ (50 mg/kg) . The experimental group was di-vided into groups with or without seizure again (B= 9) ,group B was sacrificed immediately . Seizure groups were decapitated at 0 h(C= 10) ,6 h(D= 11) ,24 h(E= 10) and 72 h(F= 10) after seizures . Blood samples were collected before scarify . Enzyme-immunoassay(EIA) was used to evaluate the chan-ges of NSE in mesencephalon ,hippocampus ,frontal cortex and serum . And the ELISA was applied to e-valuate the levels of S100B and MBP . Results The levels of S100B ,MBP and NSE in the seizure groups were significant higher than that of control group . The level of NSE in frontal cortex ,striatum and hip-pocampus of the seizure group was increased after seizure ,and the level of NSE in serum and mesencepha-lon got its highest at 6 hours after seizure ,and then decreased . At 24 hours after seizure ,the level of NSE in the hippocampus and serum was still higher then that of the control group (P〈0 .01) . Levels of S100B protein and MBP in serum ,hippocampus ,frontal lobe and mesencephalon were remarkable changes after seizure . Values of S100B protein in different brains and serum got the highest at 24 h after seizure and levels of MBP reached the highest at 72 h after seizure . Conclusion The significant increased levels of S100B protein ,MBP and NSE in the brains and serum of PTZ-induced epilepsy young rats may suggest the damage of neuron cell ,myelin fabric and glial cell .
Keywords:epilepsy  pentylenetetrazole  brain  phosphopyruvate hydratase  S100 proteins  my-elin basic proteins  rats  Sprague-Dawley
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