期刊文献+

窒息新生儿血浆NO、NOS水平及对预后的影响 被引量:1

EFFECT OF SEROUS NITRIC OXIDE AND NITRIC OXIDE SYNTHASE LEVELS ON PROGNOSIS IN ASPHYXIA NEONATORUM
暂未订购
导出
摘要 目的 探讨新生儿窒息时一氧化氮 (Nitrogenmonoxide ,NO)、一氧化氮合成酶 (Nitrogenmonoxidesyntase ,NOS)水平的变化及其对判断预后的指导意义。方法 采用比色等方法测定 32例窒息新生儿及 30例正常新生儿血浆一氧化氮、一氧化氮合成酶活性水平。结果 正常对照组NO、NOS水平分别为 (72 .84± 1 2 .35) μmol/L和 (0 .2 0 3± 0 .0 5)U/mg ,窒息组为 (1 2 9.80± 32 .66) μmol/L和(0 .352± 0 .1 2 4 )U/mg ;其中轻度窒息组为 (1 0 5 .65± 36 .30 ) μmol/L和 (0 .2 89± 0 .0 9)U/mg ;重度窒息组为 (1 4 4 .55± 2 6 .32 ) μmol/L和 (0 .364± 0 .0 1 0 )U/mg。窒息新生儿NO、NOS水平较正常新生儿明显升高 (P <0 .0 1 ) ,重度窒息患儿较轻度窒息患儿升高 (P <0 .0 1 )。结论 NO、NOS水平高低与窒息新生儿脑损伤程度和预后有关 ,可作为判断新生儿窒息及其所致新生儿缺氧缺血性脑病(HIE) Objective To investigate the levels of nitric oxide(NO) and nitric oxide synthase(NOS) in asphyxia neonatorum and its significance on prognosis judgments. Methods Levels of nitric oxide and nitric oxide synthase were measured by color matching method in 32 asphyxia neonatorums as well as 30 normal neonates. Results NO and NOS levels of the control groups were (72.84±12.35) μmol/L and (0.203±0.05)U/mg respectively,and those of the asphyxia groups were ( 129.80 ±32.66)μmol/L and (0.352±0.124)U/mg.NO and NOS levels of mild asphyxia group were (105.65±36.30)μmol/L and (0.289±0.09)U/mg,those of severe asphyxia group were (144.55±26.32)μmol/L and (0.364±0.01)U/mg respectively.No and NOS levels in asphyxia group were significantly higher than those in normal neonates(P<0.01),and those in severe asphyxia group were significantly higher than those in mild asphyxia group(P<0.01). Conclusion NO and NOS levels have relationship with the cerebral damage degree as well as the prognosis,which can be used as one of the restoration and prognosis level indications.
作者 郭洲 叶中绿
出处 《中国煤炭工业医学杂志》 2004年第6期492-493,共2页 Chinese Journal of Coal Industry Medicine
关键词 窒息新生儿 NO NOS 预后 血浆 asphyxia nitric oxide nitric oxide synthase neonatorum
  • 相关文献

参考文献3

二级参考文献17

  • 1[1]Peeters M C, Schutte B, Lenders M H, et al, Role of differential cell proliferation in the tail bud in aberrant mouse neurulation[J]. Dev Dyn, 1998,211(4):382-389.
  • 2[2]Moase C E, Trasler D G. Retinoic acid-induced selective mortality of splotch-delayed mouse neural tube defect mutants[J]. Teratology, 1987, 36(3):335-343.
  • 3[3]Lendahl U, Zimmerman L B, Mckay R D. CNS stem cells express a new class of intermediate filament protein[J]. Cell, 1990,60(4):585-595.
  • 4[4]Dahlstrand J, Lardelli M, Lendahl U. Nestin mRNA expression correlates with the central nervous system progenitor cell state in many, but not all, regions of developing central nervous system[J]. Brain Res Dev Brain Res, 1995,84(1):109-29.
  • 5[5]Griffith M, Zile M H. Retinoic acid, midkine, and defects of secondary neurulation[J]. Teratology, 2000,62(2):123-133.
  • 6[6]Geelen J A. Langman J. Closure of the neural tube in the cephalic region of the mouse embryo[J]. Anat Rec, 1977, 189(4):625-640.
  • 7[7]Harris M J, Juriloff D M. Mini-review: toward understanding mechanisms of genetic neural tube defects in mice[J]. Teratology, 1999, 60(5): 292-305.
  • 8[8]Bennett G D, An J, Craig J C, et al. Neurulation abnormalities secondary to altered gene expression in neural tube defect susceptible Splotch embryos[J]. Teratology, 1998,57(1)17-29.
  • 9[9]Okazawa H, Shimizu J, Kamei M, et al. Bcl-2 inhibits retinoic acid-induced apoptosiss during the neural differentiation of embryonal stem cells[J]. J Cell Biol, 1996,132(5):955-968.
  • 10[10]Emmanouil-Nikoloussi E N, Goret-Nicaise M, Kerameos-Foroglou C, et al. Anterior neural tube malformations induced after all-trans retinoic acid administration in white rat embryos. I. Macroscopical observations[J]. Morphologie, 2000, 84(264):5-11.

共引文献24

同被引文献1

引证文献1

二级引证文献1

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