期刊文献+

诱生型血红素氧合酶mRNA、诱生型一氧化氮合酶mRNA在脑缺血中的表达

The expression of HO-1 mRNA and iNOSmRNA in focal cerebral ischemia in rats
下载PDF
导出
摘要 目的观察诱生型血红素氧合酶(HO-1)mRNA、诱生型一氧化氮合酶(iNOS)mRNA在局灶性脑缺血中的表达及其不同作用。方法采用逆转录酶多聚酶链反应(RT-PCR)方法,测定HO-1mRNA、iNOSmRNA在局灶性缺血脑组织中不同时间点的表达变化。结果iNOSmRNA的表达在缺血后2 h出现,24 h达最高峰,以后逐渐下降。HO-1mRNA表达在缺血后2 h即出现,缺血后12 h达最高峰。结论脑缺血的病理生理过程中存在着一氧化氮(NO)及一氧化碳(CO)两种信使系统之间的相互作用。HO-1mRNA及iNOSmRNA的表达上调并具有时相性。缺血后期HO-1mRNA仍然维持在一定的水平,可能具有对抗后期iNOSmRNA增高所产生的NO毒性作用。 Objective To study the simultaneous expression of heme oxygenase (HO)-1 mRNA and inducible nitric oxide synthase (iNOS) mRNA during permanent focal cerebral ischemia in rats. Methods The expressions of HO-1 mRNA and iNOS mRNA in brains of 48 rats during permanent focal cerebral ischemia were investigated by weans of reverse transcriptase polymerase chain reaction (RT-PCR) on the basis of model of middle cerebral artery occlusion (MCAO). Results iNOS mRNA was detected in ischemic cerebral tissue at 2 h after ischemia, peaked at 24 h, then slowed down, till 7 d after MCAO. HO-I mRNA can be detected at 2 h after MCAO. The intensity of HO-I mRNA increased with time, peaked at 12 h, then slowed down till 7 d after MCAO. Conclusion The expressions of HO-I mRNA and iNOS mRNA both up-regulated and have characteristic of time course. In late stage of ischemia, the expression of HO-I mRNA to some extent protects against increasing toxicity of nitric oxide (NO) incurred by increasing iNOS mRNA.
出处 《中华神经外科疾病研究杂志》 CAS 2006年第3期236-239,共4页 Chinese Journal of Neurosurgical Disease Research
关键词 局灶性脑缺血 诱生型血红素氧合酶mRNA 诱生型一氧化氮合酶mRNA 逆转录酶多聚酶链反应 Permanent focal cerebral ischemia HO-I mRNA iNOS mRNA RT-PCR
  • 相关文献

参考文献10

  • 1Menzies SA,Hoff JT,Betz AL.Middle cerebral artery occlusion in rats:a neurological and pathological evaluation of a reproducible model[J].Neurosurgery,1992,31(1):100-107.
  • 2Samdani AF,Dawson TM,Dawson VL.Nitric oxide synthase in models of focal ischemia[J].Stroke,1997,28(6):1283-1288.
  • 3Margill I,Allix M,Boulu RG,et al.Dose-and time-dependence of L-NAME neuroprotection in transient focal cerebral ischaemia in rats[J].Br J Pharmacol,1997,120(1):160-163.
  • 4van Ginneken C,van Meir F,Sys S,et al.Stereologic description of the changing expression of constitutive nitric oxide synthase and heme oxygenase in the enteric plexuses of the pig small intestine during development[J].Br J Pharmacol,1997,437(1):118-128.
  • 5Zhang F,Kaide JI,Rodriguez-Mulero F,et al.Vasoregulatory function of the heme-heme oxygenase-carbon monoxide system[J].Am J Hypertens,2001,14(6 Pt 2):62S-67S.
  • 6Xie QW,Leung M,Fuortes M,et al.Complementation analysis of mutants of nitric oxide synthase reveals that the active site requires two hemes[J].Proc Natl Acad Sci USA,1996,93(10):4891-4896.
  • 7White KA,Marletta MA.Nitric oxide synthase is a cytochrome p-450 type hemoprotein[J].Biochemistry,1992,31(29):6627-6631.
  • 8Weiss G,Werner-Felmayer G,Werner ER,et al.Iron regulates nitric oxide synthase activity by controlling nuclear transcription[J].J Exp Med,1994,180(3):969-976.
  • 9Zhou Z,Song R,Fattman CL,et al.Carbon monoxide suppresses bleomycin-induced lung fibrosis[J].Am J Pathol,2005,166(1):27-37.
  • 10Baranano DE,Snyder SH.Neural roles for heme oxygenase:contrasts to nitric oxide synthase[J].Proc Natl Sci USA,2001,98(20):10996-11002.

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