期刊文献+

促红细胞生成素及其受体在大鼠创伤性颅脑损伤模型中的表达及意义 被引量:4

Expression and significance of erythropoietin and its receptors in rats with traumatic brain injury
原文传递
导出
摘要 目的研究创伤性颅脑损伤(TBI)大鼠损伤周围脑组织促红细胞生成素(erythropoietin,EPO)及其受体(erythropoietin receptor,EPOR)的表达。方法78只sD大鼠按随机数字表法分为对照组(6只)、假手术组(36只)、液压冲击脑创伤模型组(36只)。根据处死时间,分为6,24h和3,5,7,14d6个时相点,每个时相点假手术组和脑损伤组各处死6只大鼠,取损伤周围脑组织。利用实时荧光定量PCR和Western blot方法检测EPO、EPOR的mRNA表达和蛋白表达。结果EPO在伤后24h内即升高,到第3天达到高峰,并可维持2d左右,至伤后第7天开始下降,于伤后14d基本恢复至伤前水平;而EPOR于伤后24h到达高峰,至伤后14d表达量仍可维持较高的水平。结论TBI后24h内源性EPO及其受体的表达即开始增加,但二者的表达具有不一致性,且EPO相对受体表达具有短暂性。 Objective To study the expressions of erythropoietin (EPO) and its receptors (EPOR) in the injured brain tissue of the rats with traumatic brain injury (TBI). Methods A total of 78 SD rats were randomly divided into three groups including control group (six rats) , sham group (36 rats) and fluid percussion injury group (36 rats). The rats were sacrificed at 6,24 hours, 3,5,7 and 14 days after TBI in the sham group and the fluid percussion injury group ( six rats at each time point ). Then, the injured brain tissues were removed for observation of the mRNA and protein expressions of EPO and EPOR by means of real-time PCR and Western blot. Results The expression of EPO was increased at 24 hours and reached the peak at day 3 after TBI. The high expression level of EPO could maintain for two days or so, began to decrease at day 7 and recovered to normal at day 14 after TBI. While the expression of EPOR reached the peak at 24 hours after TB[ artd maintained high level at day 14. Conclusions The expressions of EP0 and EPOR show increase within 24 hours after TBI. In fact, the expressions of both factors are not in consistency, with more transient expression of EPO.
出处 《中华创伤杂志》 CAS CSCD 北大核心 2011年第3期206-209,共4页 Chinese Journal of Trauma
基金 天津市科技发展计划资助项目(05YFGDSF02500)
关键词 脑损伤 促红细胞生成素 受体 Brain injuries Erythropoietin Receptor
  • 相关文献

参考文献11

  • 1黄慧玲,刘锐,王琴,梁建伟,莫丽冬.亚低温对创伤性脑损伤后线粒体呼吸功能和超微结构的影响[J].中华创伤杂志,2008,24(5):350-354. 被引量:3
  • 2Parikh S, Koch M, Narayan RK, et al. Traumatic brain injury. Int Anesthesiol Clin, 2007, 45 (3) : 119 - 135.
  • 3Heegaard W, Biros M. Traumatic brain injury. Emerg Med Clin North Am, 2007, 25(3) :655 -678.
  • 4Tan CC, Eckardt KU, Firth JD, et al. Feedback modulation of renal and hepatic erythropoietin mRNA in response to graded anemia and hypoxia. Am J Physiol, 1992, 263(3 Pt 2) :Fd74 -481.
  • 5Maiese K, Chong ZZ, Li F, et al. Erythropoietin: elucidating new cellular targets that broaden therapeutic strategies. Prog Neurobiol, 2008, 85(2) :194-213.
  • 6Grasso G, Sfacteria A, Meli F, et al. Neuroprotection by erythropoietin administration after experimental traumatic brain injury. Brain Res, 2007, 1182:99 - 105.
  • 7Wallach I, Zhang J, Hartmanu A, et al. Erythropoietin - receptor gene regulation in neuronal cells. Pediatr Res, 2009, 65 ( 6 ) : 619 -624.
  • 8Sanchez PE, Navarro FP, Fares RP, et al. Erythropoietin receptor expression is concordant with erythropoietin hut not with common beta chain expression in the rat brain throughout the life span. J Comp Neurol, 2009, 514(4):403-414.
  • 9NagaiA, Nakagwa E, ChoiHB, et al. Erythropoietin and erythropoietin receptor in human CNS neuoms, astrocytes, microglia, and oligodendrocytes grown in culture. Neuor Pathol Exp Neurol, 2001, 60 (4) :386 -392.
  • 10Grasso G, Sfacteria A, Passalacqua M, et al. Erythropoietin and erythropoietin receptor expression after experimental spinal cord injury encourages therapy by exogenous erythropoietin. Neurosurgery, 2005, 56(4) :821 -827.

二级参考文献10

  • 1黎佳思,丁素菊.局灶性脑缺血大鼠脑细胞超微结构及线粒体呼吸功能变化的研究[J].中国微循环,2006,10(5):315-317. 被引量:4
  • 2Lifshitz J, Friberg H, Neumar RW, et al. Structural and functional damage sustained by mitochondria after traumatic brain injury in the rat: evidence for differentially sensitive populations in the cortex and hippocampus. J Cereb Blood Flow Metab, 2003, 23(2) :219 -231.
  • 3Verweij BH, Muizelaar JP, Vinas FC, et al. Impaired cerebral mitochondrial function after traumatic brain injury in humans. J Neurosurg, 2000, 93(5) :815 -820.
  • 4Clark JB, Nicklas WJ. The metabolism of rat brain mitochondria. Preparation and characterization. J Biol Chem, 1970, 245( 18): 4724 - 4731.
  • 5Solenski NJ, Dipierro CG, Trinner PA, et al. Ultrastructural changes of neuronal mitochondria after transient and permanent cerebral ischemia. Stroke, 2002, 33(3) :816 -824.
  • 6Singh IN, Sullivan PG, Deng Y, et al. Time course of post - traumatic mitochondrial oxidative damage and dysfunction in a mouse model of focal traumatic brain injury: implications for neuroprotective. J Cereb Blood Flow Metab, 2006, 26(11) :1407 -1418.
  • 7Vink R, Golding EM, Headrick JP. Bioenergefic analysis of oxidative metabolism following traumatic brain injury in rats. J Neurotrauma, 1994, 11(3):265-274.
  • 8Sahuquillo J, Vilalta A. Cooling the injured brain: how does moderate hypothennia influence the pathophysiology of traumatic brain injury. Curt Pharm Des, 2007, 13(22) :2310 -2322.
  • 9胡小吾,缪明永,赵麟,丁自强,王文仲,周晓平,刘建民.脑外伤后脑线粒体功能和结构改变及神经节苷脂治疗作用[J].中华神经外科杂志,1999,15(1):27-30. 被引量:23
  • 10林兆奋,缪明永.脑缺血再灌流线粒体呼吸功能的变化[J].世界急危重病医学杂志,2004,1(3):190-193. 被引量:3

共引文献2

同被引文献28

  • 1雷鹏,彭龙锋,张兴超.重组人促红细胞生成素对大鼠颅脑损伤后Survivin表达的影响[J].中国临床神经外科杂志,2007,12(6):350-353. 被引量:11
  • 2Vlodavsky E, Palzur E, Soustiel JF. Hyperbaric oxygen therapy re- duces neuroinflammation and expression of matrix metalloproteinase- 9 in the rat model of traumatic brain injury [J]. Neuropathol Appl Neurobiol. 2006, 32(1):40-50.
  • 3Grasso G, Sfacteria A, Meli F, et al. Neuroprotection by erythro- poietin administration after experimental traumatic brain injury [J]. Brain Res. 2007, 28;1182:99-105.
  • 4廖正步,支兴刚,石全红,朱继,刘北忠,钟梁.促红细胞生成素及其受体在脑外伤后的表达及意义[J].第三军医大学学报,2007,29(23):2243-2246. 被引量:6
  • 5Lu D, Mahmood A, Qu C,et al. Erythropoietin enhances neurogenesis and restores spatial memory in rats after traumatic brain injury[J]. J Neurotrauma,2005,22(9):1011-1017.
  • 6Parikh S, Koch M,Narayan RK. Traumatic brain injury[J]. Int Anesthesiol Clin,2007,45(3):119-135.
  • 7Heegaard W, Biros M. Traumatic brain injury[J]. Emerg Med Clin North Am,2007,25(3):655-678.
  • 8Wallach I,Zhang J, Hartmann A, et al. Erythropoi-etin-receptor gene regulation in neuronal cells[J]. Pe-diatr Res,2009,65(6):619-624.
  • 9Sanchez PE, Navarro FP, Fares RP, et al. Erythropoietin receptor expression is concordant with erythropoietin but not with common beta chain expression in the rat brain throughout the life span[J]. J Comp Neurol,2009,514(4):403-414.
  • 10Nagai A, Nakagawa E,Choi HB, et al. Erythropoietin and erythropoietin receptors in human CNS neurons,astrocytes, microglia, and oligodendrocytes grown in culture[J]. J Neuropathol Exp Neurol,2001,60(4):386-392.

引证文献4

二级引证文献6

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