期刊文献+

硫化氢对海洛因依赖大鼠一氧化氮/一氧化氮合酶体系的影响 被引量:2

The effect of hydrogen sulfide on nitric oxide /nitric oxide synthase system in heroin dependent rats
下载PDF
导出
摘要 目的探讨硫化氢(H2S)对海洛因依赖大鼠一氧化氮(NO)/一氧化氮合酶(NOS)体系的影响。方法实验大鼠随机分成3组:正常对照组、海洛因依赖组(herion组)、海洛因依赖+NaHS组(heroin+NaHS组)。采用比色法测定大鼠血浆及海马组织NO含量,Real time PCR测定海马组织nNOS mRNA表达量。结果血浆及海马NO含量比较,herion组与heroin+NaHS组均高于对照组(<0.05),heroin+NaHS组低于herion组(<0.05);海马组织nNOS mRNA表达量比较,herion组高于对照组(<0.05),heroin+NaHS组与对照组无显著差异(>0.05),heroin+NaHS组低于herion组(<0.05)。结论海洛因依赖可导致大鼠体内NO水平升高,H2S供体NaHS可抑制NO的产生,下调nNOS mRNA表达。 Objective To explore the effect of hydrogen sulfide (H2S) on nitric oxide (NO) /nitric oxide synthase (NOS) system in heroin dependent rats. Methods Experimental rats were divided into three groups: control group, heroin group and heroin + NariS group. The level of NO in plasma and hippocampus was detected by the spectrophotometer method. The expression ofrtNOS mRNA was observed by Real time PCR. Results Compared with control group, NO in plasma and hip- pocampus increased (P 〈 0.05) in heroin group and heroin+NariS group, the expression ofnNOS mRNA up-regulated (P 〈 0.05) in heroin group. Compared with heroin group, NO in plasma and hippocampus decreased (P 〈 0.05) and the expression ofnNOS mRNA down-regulated (P 〈 0.05) in heroin+NariS group. Conclusion Heroin dependence can increase NO level and up-regulate the expression ofnNOS mRNA in rats. Exogenous H:S donor NariS can inhibit the production of NO and down-regulate the expression ofnNOS mRNA.
出处 《遵义医学院学报》 2011年第6期572-575,共4页 Journal of Zunyi Medical University
基金 贵州省高层次人才科研条件特助经费项目(NO:TZJF-2008-59)
关键词 海洛因依赖 海马 硫化氢 一氧化氮 一氧化氮合酶 heroin dependence hippocampus hydrogen sulfide nitric oxide nitric oxide synthase
  • 相关文献

参考文献8

二级参考文献58

共引文献35

同被引文献40

  • 1钟星明,江丽霞,刘春棋.葛根素对大鼠抗氧化酶活性作用的研究[J].赣南医学院学报,2006,26(4):485-486. 被引量:15
  • 2罗标文.海洛因依赖急性脱毒期6例猝死病例分析[J].中国药物依赖性杂志,2007,16(4):320-320. 被引量:3
  • 3Goodwin LR,Francom D,Dieken FP,et al. Determination of sulfide inbrain tissue by the gas dialysision chromatography : postmortem stuies andtwo case reports[J]. Anal Toxicol, 1989,13(2) : 105-109.
  • 4Warenycia MW, Goodwin LR, Benishin CG,et ai. Acute hydrogen sulfidepoisoning: demonstration,of selective uptake of sulfide by the brainstemby measurement of brain sulfide levels[J]. Biochen Pharmacol, 1989,38(6):973-981.
  • 5Awata S,Nakayama K,Suzuki I, et al. Changes in cystathionine gammatyasein various regions of rat brain during development[J]. Biochem Mol Bio Int,1995,35(6):1331-1338.
  • 6Singh S,Banerjee R. PLP-dependent H(2)S biogenesis[J]. Biochim Bio-phys Acta,2011,1814(11 ):1518-1527.
  • 7Abe K, Kimura H. The possible role of hydrogen sulfide as an endougenousneuromodulator[J]. Neurosic,1996,16(3) : 1066-1071.
  • 8Sbibuya N, Mikami Y, Kimura Y, et al. Vascular endouthelium expresses3-mercaptopyruvate sulfurtransferase and produces hydrogen sulfide [J].Biochem,2009,146(5) :623-626.
  • 9Fume J, Saeed A, Levitt MD. Whole tissue hydrogen sulfide concentra-tions are orders of magnitude lower than presently accepted values[J]. Phy-siol Regul Integr Comp Physiol, 2008,295 (5) :R1479-1485.
  • 10Whitfield NL,Kreimier EL, Verdial FC, et al. Reappraisal of H2S/sulfideconcentration in vertebrate blood and its potential significance in ischemicpreconditioning and vascular signaling[J]. Physiol Regul Integr Comp Physiol,2008,294(6) :R1930-1937.

引证文献2

二级引证文献3

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