期刊文献+

贴敷式头部亚低温不同时间窗对新生仔兔HIBD治疗时NSE变化的研究 被引量:1

NSE study in different time windows of cephalic--applied sub--hypothermia in HIBD therapy in newborn rabbits
原文传递
导出
摘要 目的通过贴敷式头部亚低温不同时间窗对新生仔兔HIBD(缺血缺氧性脑病)治疗前后血中NSE(神经元特异性烯醇化酶)的测定,揭示贴敷式头部亚低温对新生仔兔HIBD有保护作用。方法采用酶联免疫法测定不同时间窗时间的血清中NSE。贴敷式头部亚低温实施6h治疗。结果HIBD后不同时间窗组及假手术组(正常组)组间比较,血清中NSE含量有显著差异(P〈0.01),经q检验进行两两比较发现,HIBD后3h组NSE含量与正常组未见显著差异(P〉0.05),而HIBD后其他组与正常组间均有显著性差异。结论贴敷式头部亚低温对缺血缺氧性脑病有保护作用;HIBD后不同时间窗均有脑保护作用,但HIBD后3h组脑保护作用最强。 Objective To explore the protective effect of sticking--type head cooling, by measuring the content of the NSE in different time windows of cephalic--applied sub--hypothermia in the HIBD therapy in newborn rabbits. Methods a cephalic-- applied sub-- hypothermia was administered to new- born rabbits for 6 hours, while gauging the NSE concentration in serum in different time windows by ELISA (enzyme linked immunosorbent assay). Results There is a significant difference in NSE concentration between false--operational group(the normal group) and diverse time--window groups (P〈 0.01 ). No significant difference was detected in the NSE concentration between the normal group and the three--hour--after--HIBD group by Q Test (P〉0.05), whereas other post--HIBD groups did have significant differences from the normal group. Conclusions Cephalic--applied sub--hypothermia contrib- uted to the protection of HIBD, that carries out its function in different time windows,among those the three--hours being the most powerful one.
出处 《神经疾病与精神卫生》 2011年第3期268-270,共3页 Journal of Neuroscience and Mental Health
关键词 磷酸丙酮酸水含酶 贴敷式头部亚低温 NSE 脑保护 时间窗 Phosphopyruvate hydratase Cephalic--applied sub--hypothermia NSE Brain protection Time windows
  • 相关文献

参考文献5

二级参考文献75

  • 1选择性头部亚低温治疗新生儿缺氧缺血性脑病多中心协作组.选择性头部亚低温治疗新生儿缺氧缺血性脑病安全性临床多中心研究[J].中国循证儿科杂志,2006,1(1):20-25. 被引量:16
  • 2选择性头部亚低温治疗新生儿缺氧缺血性脑病多中心协作组,邵肖梅.选择性头部亚低温治疗新生儿缺氧缺血性脑病多中心临床研究阶段性疗效分析[J].中国循证儿科杂志,2006,1(2):99-105. 被引量:65
  • 3De Giorgio CM, Gott PS, Rabinowicz AL, et al . Neuronspecific enolase, a marker of acute neuronal injury, is increased in complex partial status epilepticus [J]. Epilepsia, 1996, 37(7): 606-609.
  • 4Kukacka J, Vajtr D, Huska D, et al . Blood metallothionein, neuron specific enolase, and protein S100B in patients with traumatic brain injury [J]. Neuro Endocrinol Lett, 2006, 27 (2): 116-120.
  • 5Kaiser E, Kuzmits R, Pregant P, et al . Clinical biochemistry of neuron-specific enolase [J]. Clin Chim Acta, 1989, 183: 13-32.
  • 6Anastasiades KD, Mullins RE, Conn RB. Neuron-specific enolase. Assessment by ELISA in patients with small cell carcinoma of the lung [J]. Am J Clin Pathol, 1987, 87: 245-249.
  • 7Joseph J, Cruz-Sanchez FF, Carreras J, et al . Enolase ctivity and isoenzyme distribution in human brain regions and tumors [J]. J Neurochem, 1996, 66: 2484-2490.
  • 8Vos PE, Lamers K J, Hendriks JC, et al . Glial and neuronal proteins in serum predict outcome after severe traumatic brain injury [J]. Neurology, 2004,62(8): 1303-1310.
  • 9Pineda JA,Wang KK, Hayes RL. Biomarker of proteolytic damage following traumatic brain injury [J]. Brain Pathol, 2004, 14(2): 202-209.
  • 10Gross J, Ungethum U, Andreeva N, et al . Glutamate-induced efflux of protein, neuron-specific enolase and lactate dehydrogenase from a mesencephalic cell culture [J]. Eur J Clin Chem Clin Biochem,1996, 34: 305-310.

共引文献54

同被引文献16

  • 1Shen L, Nam H, Song P, et al. Foxgl haploinsufficiency results in impaired neurogenesis in the postnatal hippocampus and contextual memory deficits. Hippocampus,2006, 16 :875-890.
  • 2DomanskaJK, Buzanska L, Lukomska B. A novel, neural potential of non-hematopoietic human umbilical cord blood stem cells. IntJ Dev Bioi, 2008,52 :234-237.
  • 3RiceJE, Vannucci RC, BriedeyJB, et al. The infuence of immaturity on hypoxic ischemic brain damage in the rat. Ann Neurol, 1981,9: 131-141.
  • 4Fasano CA, Phoenix TN, Kokovay E, et al. Bmi-I cooperates with Foxgl to maintain neural stem cell self-renewal in the forebrain. Genes Dev, 2009,23 :561-574.
  • 5Hwang CH, Simeone A, Lai E, et al. Foxgl is required for proper separation and formation of sensory cristae during inner ear develop-ment. Dev Dyn, 2009,238: 2725-2734.
  • 6Kawauchi S, Santos R, KimJ et al. The role of Foxgl in the develop-ment of neural stem cells of the olfactory epithelium. Ann NY Acad Sci 2009,1170 :21-27.
  • 7SiegenthalerJA, Tremper-Wells BA, Miller MW. Foxgl haploinsuffi-ciency reduces the population of cortical intermediate progenitorcells , Effect of increased p21 expression. Cereb Cortex, 2008, 18: 1865- 1875.
  • 8Kennea NL, Mehmet H. Perinatal applications of neural stem cells. Best Pract Res Clin Obstet Gynaecol ,2004,18 :977 -994.
  • 9Nakayama D, Matsuyama T, Ishibashi-Veda H, et al. Injury induced neural steml progenitorcells in post-stroke human cerebral cortex. EurJ Neurosci ,2010 ,31 :90-98.
  • 10Bedard A, Parent A. Evidence of newly generated neurons in the human olfactory bulb. Brain Res Dev Brain Res,2004,151 :159-168.

引证文献1

二级引证文献5

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