期刊文献+

大鼠弥漫性脑损伤神经元HSP70表达及神经髓鞘的病理变化 被引量:2

An experimental study of HSP70 expression and morphology of myelin sheath after diffuse brain injury in rats
下载PDF
导出
摘要 目的探讨脑神经元HSP70表达变化和神经髓鞘病变在弥漫性脑损伤(DB I)诊断及其损伤时间判断的价值。方法将50只SD大鼠分为正常对照组和DB I组,后者按DB I后处死大鼠的时间不同又分为0.5h、1h、3h、6h、12h、1d、3d、7d及10d组。然后复制大鼠DB I模型,脑组织常规取材后进行HSP70免疫组化及劳克坚牢蓝(LFB)髓鞘染色,观察神经元HSP70的变化和神经髓鞘病变。结果大鼠DB I后0.5h,脑干及海马处见HSP70免疫组化染色阳性的神经元;伤后1h明显,12h达到高峰,1d下降,7d基本恢复正常。神经髓鞘于伤后0.5h开始逐渐出现水肿,分层、碎裂及聚集成团块状,伤后1d最明显,3d后开始逐渐减退,10d基本正常。结论神经元HSP70表达变化和神经髓鞘病变程度对DB I诊断及其损伤时间判断具有一定的参考价值。 Objective To study HSP70 expression and morphological changes of myelin sheath in rat after experimental DBI in order to explore a useful method to estimate the injury time of DBI. Methods Fifty SD rats were divided into a normal control and 9 different injury groups at 0.5h, lh, 3h, 6h,12h,ld, 3d,7d, 10d after the DBI. The animal models of DBI was made according to the method described by Marmarou. The HSP70 expression and the morphological changes of myelin sheath in each groups were observed by immunohistochemical ( SABC method) and LFB staining. Results In brain tissue of normal control group, no significant change was found. In the brain tissues of injury groups, the HSP70 expression showed a time-dependent difference as fellows: It began at 0.5h, increased at 3h and reached to maximize at 12h, then decreased, and returned to the basal level on 1 d. Meanwhile, the morphologic changes of myelin sheath stained by LFB showed edema, delamination, broken and collected into piles in brain stem at 0.5h, those morphological changes reached the peak on ld, decreased and began reparation on 3d, and recovered to normal station basically on 10d after the DBI. Conclusion The HSP70 expression and morpho- logical changes of myelin sheath in rat observed by immunohistochemical and LFB staining can be used to help the diagnosis of DBI and estimation of injury time of DBI
出处 《中国法医学杂志》 CSCD 2007年第3期163-165,F0003,共4页 Chinese Journal of Forensic Medicine
关键词 法医病理学 弥散性脑损伤(DBI) 损伤时间推断 热休克蛋白70(HSP70) 髓鞘病变 Forensic pathology Diffuse brain injury Estimating injury time HSP70 Myelin sheath
  • 相关文献

参考文献8

  • 1朱金龙,朱少华,任亮,刘良,周亦武,陈虎,邓伟年.大鼠弥散性轴索损伤后β-APP的表达[J].法医学杂志,2005,21(3):165-168. 被引量:9
  • 2Marmarou A,Foda M A,van den Brink W,et al.A new model of diffuse brain injury in rats.Part Ⅰ:Pathophysiology and biomechanics[J].J Neurosurg,1994,80:291 -300.
  • 3Montasser A,Abd-Elfattah Foda M S,Marmarou A,et al.A new model of diffuse brain injury in rats.Part Ⅱ:Morphological characterization[J].J Neurosurg,1994,80:301 -313.
  • 4郝春荣,任大宏,刘绍春.皮肤组织神经髓鞘几种染色方法的比较[J].中国组织化学与细胞化学杂志,2001,10(3):320-322. 被引量:1
  • 5Velazquez J M,Lindquist S.HSP70 nuclear concentration during environmental stress and cytoplasmic storage during recovery[J].Cell,1984,36:655-662.
  • 6Dutcher S A,Underwood B D,Walker P D,et al.Patterns of heat-shock protein 70 biosynthesis following human traumatic brain injury[J].J Neurotrauma,1998; 15(6):411 -20.
  • 7王慧君,饶广勋,朱少华,秦启生.HSP70、NF应用于脑挫伤时间推断的实验研究[J].法医学杂志,2000,16(3):132-134. 被引量:13
  • 8Virley D,Hadingham S J,Roebert J C,et al.A new primate model of focal stroke:endothelin-induced middle cerebral artery occlusion and reperfusion in the common marmoset[J].J Cereb Blood Flow Metab,2004,24(1):24-41.

二级参考文献24

  • 1王子慧.人脊髓创伤后神经元病变的神经丝免疫组织化学研究[J].中国组织化学与细胞化学杂志,1995,4(2):134-138. 被引量:6
  • 2杜卓民,实用组织学技术(第2版),1998年
  • 3田玉旺,中国组织化学与细胞化学杂志,1994年,3卷,3期,272页
  • 4凌启波,实用病理特殊染色和组化技术,1989年,161页
  • 5张益鹄 黄光照 麻永昌.弥散性轴索损伤[A].黄光照,麻永昌.中国刑事科学技术大全·法医病理学[M].北京:中国人民公安大学出版社,2002.265-267.
  • 6Marmarou A, Foda MA, Van den Brink W, et al. A new model of diffuse brain injury in rats.Part Ⅰ: Pathophysiology and biomechanics[J]. J Neurosurg, 1994,80:291-300.
  • 7Montasser A, Abd-Elfattah Foda MS, Marmarou A, et al. A new model of diffuse brain injury in rats. Part Ⅱ: Morphological characterization[J]. J Neurosurg, 1994,80:301-313.
  • 8同济医科大学病理学教研室.病理组织学技术[M].武汉:湖北科学技术出版社,1986.124-125.
  • 9卿太苏 刘世沧 汪秉康 侯一平 刘世沧.弥漫性轴索损伤的法医病理学研究[A].侯一平,刘世沧.法医学进展与实践(第一卷)[M].成都:成都科技大学出版社,1997.36-39.
  • 10Stone JR, Singleton RH, Povlishock JT, et al.Intra-axonal nerurofilament compaction dose not evoke local axonal swelling in all traumatically injured axons[J]. Experimental Neurology, 2001,172(2):320-331.

共引文献20

同被引文献31

引证文献2

二级引证文献7

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