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褪黑素对缺血再灌注后大鼠肝脏NF-κB表达及iNOS的影响

The Influence of Melatonin on the Expression of NF-κB and iNOS in Rat Liver After Ischemia and Reperfusion
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摘要 目的探讨褪黑素对缺血再灌注后大鼠肝脏NF-κB表达及iNOS的影响.方法采用大鼠部分肝缺血再灌注模型,将健康雄性SD大鼠78只随机分为假手术组(S)、缺血再灌注组(I/R)、褪黑素处理组(Mel)3组,分别检测标本中NF-κB表达和iNOS含量.结果S组无NF-κB阳性表达;I/R组和Mel组经历单纯的肝脏缺血后,NF-κB的表达与S组无差异(P>0.05),而再灌注后两组均有不同程度的NF-κB表达增加,并均于6 h时点处达到各自峰值,Mel组于再灌注后各相应时点NF-κB的阳性表达率显著低于I/R组(P<0.01).再灌注后0~1 h,3组iNOS活力无差异(P>0.05),此后,I/R组iNOS活力随再灌注时间的延长而较S组显著上升(P<0.01),其高峰亦在9 h时点处出现,Mel组再灌注1 h后各时点iNOS活力均较I/R组显著下降(P<0.01).结论褪黑素可以有效下调肝脏I/R过程中NF-κB的表达,抑制iNOS的活力,发挥其对肝脏缺血再灌注损伤的保护作用. Objective To explore the influence of in rat liver after ischemia and reperfusion. Methods melatonin on the expression of NF-κB and iNOS With a rat model of partial hepatic ischemia and reperfusion, 78 healthy male SD rats were randomized into 3 groups: sham-operation group(s), ischemia/reperfusion group(I/R), melatonin group(Mel). The expression of NF-κB was evaluated and the measurement of iNOS was carried out. Results There was no expression of NF-κB in S group; After ischemia without reperfusion, the expression of NF-κB in both I/R group and Mel group was no statistic significance compared with S group(P 〉0.05), however, the expression of NF-κB in both I/ R group and Mel group increased and reached the top at 6 h time point during the reperfusion period. The expression of NF-κB in Mel group were significantly lower than that in the I/R group at each corresponding time point during reperfusion (P 〈 0.01). 0-1 h after reperfusion, there was no difference among three groups (P〉0.05). At each following time point, the activity of iNOS in I/R group was much higher than that in the S group(P〈0.01)and reached the top at 9 h time point. The activity of iNOS in Mel group was significantly lower than that in the I/R group at each corresponding time point after 1 h(P 〈 0.01). Conclusion Melatonin can down-regulate the expression of NF-κB and depress the activity of iNOS during the ischemia and reperfusion period and protect the liver from ischemia and reperfusion injury.
作者 张楷 吴浩荣
出处 《苏州大学学报(医学版)》 CAS 北大核心 2005年第4期563-566,共4页 Suzhou University Journal of Medical Science
关键词 褪黑素 核因子-ΚB 诱导型一氧化氮合酶 缺血再灌注损伤 melatonin nuclear factor-κB inducible Nitric Oxide synthase ischemia and reperfusion injury
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参考文献11

  • 1张宁.一氧化氮对核因子-κB的反馈调节作用[J].国外医学(呼吸系统分册),2002,22(2):66-69. 被引量:5
  • 2Nauta R J, Tsimoyiannis E, Uribe M, et al. Oxygen-derived free radicals in hepatic ischemia and reperfusion injury in the rat[J]. Surg Gynecol Obstet, 1990, 171: 120 -125.
  • 3Hur GM, Ryu YS, Yun HY, et al. Hepatic ischemia/ reperfusion in rats induces iNOS gene transcription by activation of NF-kB[J]. Biochem Biophys Res Commun, 1999, 261: 917 - 22.
  • 4Tan DX, Manchester LC, Burkhardt S, et alN-acetyl-Nformyl-5-metoxykynuramine, a biogenic amine and melatonin metabolite, functions as a potent antioxidant [J ]. FASEB J, 2001, 15:2294 - 2296.
  • 5Shen Zhang, Wei Li, Qiuhua Gao, et al. Effect of mela tonin on the generation of nitric oxide in murine macrophages [ J ]. European Journal of Pharmacology, 2004, 501:25 - 30.
  • 6Xiong S, She. Signaling role of intracellular iron in NFκB activation [J]. J Biol Chem, 2003, 278: 17646 - 17654.
  • 7Lipton S A, Choi. A redox-based mechanism for the neuroprotective and neurodestructive effects of nitric oxide and related nitroso-compounds [J ]. Nature, 1993, 364: 626 - 632.
  • 8Umansky V, Hehner SP, Dumont A, et al. Co-stimulatory effect of nitric oxide on endothelial NF-kappaB implies a physiological self-amplifying mechanism. Eur J Immunol, 1998, 28(8) :2276 - 2282.
  • 9Koeppel TA, Thies JC, Schemmer P, et al. Inhibition of nitric oxide synthesis in ischemia/reperfusion of the rat liver is followed by impairment of hepatic microvascular blood flow[J]. J Hepatol, 1997, 27:163 - 169.
  • 10Turjanski AG, Saurz DA, Doctorovich F, et al Nitrosation of melatonin by nitric oxide: a computational study[J]. J Am Chem Soc 2001, 37:97- 101.

二级参考文献20

  • 1Peng HB,et al.J Biol Chem,1995;270:14214-14219
  • 2Spiecker M,et al.J Bio Chem,1997 ; 272: 30969-30974
  • 3PengHB,etal.J Immunol,1998;161:1970-1976
  • 4Shin WS,et al.J Bio Chem,1996;271:11317-11324
  • 5Chen F,et al.AmJ Pathol,1999;155:275-284
  • 6Schroeder RA,et al.Am J Physiol,1999;277:C523-530
  • 7Welters ⅡD,et al.Anesthesiology,2000;92:1677 - 1684
  • 8Snead C,et al.J Bio Chem,1998;273:3895 -3900
  • 9Colasanti M,et al.Brain Res Bull,2000;52:155- 161
  • 10Togashi H,et al.Prlc Natl Acad Sci USA,1997;94:2676-2680

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