期刊文献+

脑缺血后髓鞘基因表达变化的规律 被引量:8

mRNA expression change of myelin gene in hippocampus following cerebral ischemia
原文传递
导出
摘要 目的从髓鞘碱性蛋白(MBP)mRNA、髓鞘少突胶质糖蛋白(MOG)mRNA等髓鞘基因表达的角度,探讨脑缺血大鼠髓鞘损伤的变化规律。方法采用SD大鼠四血管闭塞急性全脑缺血模型,随机分为2 d、4 d、7 d、14 d和28 d五个时间点及假手术组,每组8只;用逆转录聚合酶链式反应(RT-PCR)观察海马组织中MBP mRNA、MOG mRNA表达的变化。结果脑缺血后2 d海马组织中MBP mRNA、MOG mRNA表达水平即已降低,至7 d时降低显著,并持续至28 d时达到高峰。与假手术组比较,大鼠海马组织内MBP mRNA、MOG mRNA表达于再灌流后7 d、14 d、28 d差异具有统计学意义(P<0.05)。结论随着脑缺血-再灌流时间延长,大鼠海马组织MBP mRNA、MOG mRNA表达逐渐降低,呈现时间依赖性。 Objective To study the mRNA expression of myelin basic protein (MBP) and myelin oligodendroglia glyeoprotein (MOG) in hippocampus of rats following global brain ischemia. Method The four- vessel occlusion animal model in the Sprague-Dawley rats was used in this study, The mRNA expression levels of MBP and MOG in the hippocampus of rats were analyzed by reverse transcription polymerase chain reaction ( RT- PCR) at day 2, 4, 7, 14 and 28 days after global brain ischemia, There were eight rats at each time-point and sham operated group. Results The mRNA expression of both MBP and MOG in hippocampus of rats decreased at 2 days after global brain ischemia, The gene expression of myelin gene decreased significantly at 7 days and it reached to the lowest level at 28 days. Compared with sham operated group, the gene expression of MBP and MOG in hippocampus of rats decreased significantly at 7, 14 and 28 days after global brain ischemia ( P 〈 0.05). Conclusions The down-regulation of MBP mRNA and MOG mRNA was time dependent in hippocampus following transient global ischemia in rats.
出处 《中华急诊医学杂志》 CAS CSCD 2007年第9期929-932,共4页 Chinese Journal of Emergency Medicine
基金 江苏省卫生厅重大科研课题资助项目(K200406) 苏州大学医学发展基金(EE123504)
关键词 髓鞘基因 全脑缺血 海马 逆转录聚合酶链式反应 Myehn gene Cerebral ischemia Hippocampus RT-PCR
  • 相关文献

参考文献13

  • 1Adams H, Adams R, Zoppo GD, et al. Guidelines for the early management of patients with ischemic [J]. Stroke, 2005, 36 (4): 916-923.
  • 2Tanaka K, Nogawa S, Suzuki S, et al. Upregulation of oligodendrocyte progenitor cells associated with restoration of mature oligodendrocytes and myelination in peri-infarct area in the rat brain [J]. Brain Res, 2003, 989 (2): 172-179.
  • 3陈应柱,包仕尧,田野.少突胶质细胞与缺血性脑损伤[J].国外医学(脑血管疾病分册),2005,13(5):367-370. 被引量:8
  • 4Pulsinelli WA, Beierly JB. A new model of bilateral hemispheric ischemia in the unanesthetized rat [J]. Stroke, 1979, 10 (4): 267- 270.
  • 5陈应柱,许俊,袁成林,吕庆康,包仕尧.大鼠缺血脑组织芯片的构建[J].中国脑血管病杂志,2006,3(11):504-507. 被引量:6
  • 6Kurosinski, G. Glial cells under physiologic and pathologic conditions [J]. Arch Neural, 2002, 59 (10): 1524-1528.
  • 7Back SA, Han BH, Iaao NL, et al. Selective vulnerability of late oligodendrecyte progenitors to Hypoxia/ischemia [J]. J Neurosci, 2002, 22 (2): 455-463.
  • 8Dawson MR, Polito A, Levine JM, et al. NG2-expressing glial progenitor cells: an abundant and widespread population of cycling cells in the adult rat CNS [J]. Mol Cell Neurosci, 2003, 24 (2): 476- 488.
  • 9Sato G, Tanaka R, Akiyama K, et al. lmmunohistochemical analysis of myelination following hemicranial irradiation in neonatal rats [J]. Neurosci Lett, 2003, 353 (2): 131-134.
  • 10Banmann N, Pham-Dinh D. Biology of oligodendrocyte and myelin in the mammalian central nervous system [J]. Physiol Rev, 2001, 81 (2): 871-927.

二级参考文献34

  • 1孙彦辉,张亚卓,王忠诚,孙梅珍,赵东海.MGMT在脑胶质瘤组织中的表达及其与患者生存期的关系[J].癌症,2004,23(9):1052-1055. 被引量:36
  • 2韩伟,张春庆,戚基萍,李丹阳.应用组织芯片技术研究IGF-1在反应性和肿瘤性星形胶质细胞中表达的区别[J].肿瘤防治研究,2006,33(6):394-396. 被引量:1
  • 3王清良,卞修武,章容,蒋雪峰.星形细胞肿瘤微血管组织芯片的构建和微血管壁组成细胞研究[J].临床与实验病理学杂志,2006,22(4):440-443. 被引量:3
  • 4[2]Moch H,Kononen T,Kallioniemi OP,et al.Tissue microarrays:what will they bring to molecular and anatomic pathology? Adv Anat Pathol,2001,8:14-20.
  • 5[3]Pulsinelli WA,Beierly JB A new model of bilateral hemispheric ischemia in the unanesthetized rat.Stroke,1979,10:267-272.
  • 6[8]Martikainen P,Louhelainen AM,Kauppinen T,et al.Human brain tissue microarrays as a platform to investigate diseases of the nervous system.Brain Res,2006,1089:33-43.
  • 7[9]Preuss TM,Caceres M,Oldham MC,et al.Human brain evolution:insights from mieroarrays.Nat Rev Genet,2004,5:850-860.
  • 8[10]Soverchia L,Ubaldi M,Leonardi-Essmann F,et al.Microarrays-the challenge of preparing brain tissue samples.Addict Biol,2005,10:5-13.
  • 9[12]Kononen J,Bubendorf L,Kallionieni A,et al.Tissue microarrays for high-throughput molecular profiling of tumor specimens.Nat Med,1998,4:844-847.
  • 10Back SA, Han BH, Luo NL, et al. Selective vulnerability of late oligodendrocyte progenitors to hypoxia-ischemia. J Neurosci, 2002, 22:455 - 463.

共引文献12

同被引文献100

引证文献8

二级引证文献16

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部