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JAK抑制剂AG490对大鼠组织iNOS和NO合成的影响 被引量:1

Effects of janus kinase/signal transducer and activator of transcription pathway on synthesis of iNOS and NO in pulmonary and vascular tissues of infectious shock rats
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摘要 目的观察JAK/STAT通路对脓毒症大鼠组织和血清诱导型一氧化氮合成酶(iNOS)和一氧化氮(NO)合成的影响。方法采用盲肠结扎穿孔术(cecal ligation puncture,CLP)制造大鼠脓毒症模型,将48只Wistar大鼠随机分为正常对照组、假手术组、CLP脓毒症组和AG490处理组。分别采集正常对照组、假手术组以及CLP组和AG490组2、6、24h的组织和血清,采用RT-PCR测定组织iNOS mRNA表达水平,NO检测试剂盒(酶法)检测组织和血清NO含量;同时分别监测上述各时间点的平均动脉压、脉搏。结果正常组大鼠血清、肺和血管含有少量iNOS mRNA和NO,与正常组大鼠相比,假手术组iNOS mRNA和NO的含量均未见明显差别,CLP后各时间点肺、血管和血清iNOS mRNA、NO含量均升高明显;而MAP严重下降、脉搏剧烈升高(P<0.05,P<0.01)。AG490处理组与CLP组相应时间点相比,肺、血管和血清多个时间点iNOS mRNA表达和NO含量均显著下降;血压和脉搏均显著好转(P<0.05,P<0.01)。相关分析显示:肺和血管组织NO与iNOS mRNA的相关系数分别是0.75和0.73;血清与NO与肺、血管组织iNOS mRNA的相关系数分别是0.68和0.62(P<0.05),MAP与肺、血管和血浆NO的相关系数分别是-0.85、-0.86和-0.91(P<0.05)。结论抑制JAK/STAT通路活化可抑制脓毒症大鼠血浆和组织iNOS mRNA和NO合成;并改善循环功能。 Objective To determine the effects of janus kinase/signal transducer and activator of transcription on the synthesis of inducible nitric oxide synthase (iNOS) and nitric oxide (NO) in infectious shock rats. Methods Forty-eight male Wistar rats were randomly divided into normal control, sham operation group, cecal ligation puncture (CLP) group, and inhibitor of JAK (AG490) treatment group. CLP group and AG490 group were established into the sepsis model induced by CLP, and at 2, 6, 24 h after CLP, the rats were sacririced. The pulmonary, vascular tissues and serum samples of all rats were harvested to determine iNOS mRNA expression levels by reverse transcription polymerase chain reaction (RT-PCR) and NO content respectively. Meanwhile, the mean arterial pressure (MAP) and pulse were monitored. Results No notable difference was detected in all parameters between sham operation group and normal control. Compared with normal control, iNOS mRNA and NO levels in pulmonary, vascular tissues and serum at 2, 6 and 24 h following CLP significantly elevated respectively, and MAP fell notably and pulse increased (P 〈 0.05 or 0.01 ). AG490 treatment decreased iNOS mRNA and NO levels markedly at 2 or 6 h after CLP, meanwhile MAP and pulse deteriorated by sepsis were also ameliorated ( P 〈 0.05 or 0.01 ). Conclusion Inhibiting the activation of JAK/STAT pathway can reduce tissues and serum iNOS mRNA and NO expressions in infectious shock rats and can ameliorate the circulatory function deteriorated by sepsis.
机构地区 解放军 解放军
出处 《第三军医大学学报》 CAS CSCD 北大核心 2007年第15期1511-1513,共3页 Journal of Third Military Medical University
关键词 Janus激酶抑制剂/AG490 NO 脓毒症 JAK/STAT信号通路 大鼠 INOS janus kinase inhibitor/AG490 nitric oxide infectious shock JAK/STAT pathway rat inducible nitric oxide synthase
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  • 1黎冬暄,田伏洲,李红,李旭,罗皓,向珂.胰弹性蛋白酶对内毒素诱导的肝枯否细胞TNF-α、IL-1β表达的影响[J].解放军医学杂志,2004,29(9):801-802. 被引量:6
  • 2郑岩,包进,赵宝友.全身炎症反应综合征患儿血清TNF-α、IL-10含量的观察[J].中国妇幼保健,2004,19(12):85-86. 被引量:3
  • 3曹敏,孙荣奇,吴达俊,沈平孃,袁雅美.中药雷公藤的研究进展[J].中成药,1996,18(4):40-42. 被引量:30
  • 4Miscia S, Marchisio M, Grilli A, et al.Tumor necrosis factor alpha (TNF - α activates Jakl/Stat3 - Stat5B signaling throu-gh TNFR - 1 in human B cells [J].Cell Growth Differ,2002,13(1) : 13 - 18.
  • 5Riley J K, Takeda K, Akira S, et al. Interleukin- 10 receptor signaling through the JAK - STAT pathway [J]. J Biol Chem, 1999,274(23) : 16513 - 16521.
  • 6Jacobs A T, Ignarro L J. Lipopolysaccharide -induced expression of interferonbeta mediates the timing of inducible nitric- oxide synthase induction in RAW 264. 7 macrophages [J]. J Biol Chem, 2001,276(51),47950 - 47957.
  • 7Stoiber D,Stockinger S, Steinlein P ,et al. Listeria monocytogenes modulates macrophage cytokine responses through STAT serine phosphorylation and the induction of suppressor of cytokine signaling[J]. J Immunol,2001,166(1) :466 - 472.
  • 8Dell'Albani P, Santangelo R, Torrisi L,et al. JAK/STAT signaling pathway mediates cytokine - induced iNOS expression in primary astroglial cell cultures[J]. J Neurosci Res, 2001, 65(5),417-424.
  • 9Held T K, Weihua X, Yuan L, et al.Gamma interferon augments macrophage activation by lipopolysaccharide by two distinct mechanisms, at the signaltransduction level and via an autocrine mechanism involving tumor necrosis factor alpha and interleukin - 1 [J].Infect Immun, 1999,67 (1) : 206 - 212.
  • 10Benkhart E M, Siedlar M, Wedel A, et al. Role of STAT3 in lipopolysaccharide - induced IL - 10 gene expression [J]. J Immunol,2000,165(3):1612 - 1617.

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  • 1胡钢英,王晋明,江洪,邓汉华,梁远红.螺内酯和缬沙坦对高血压大鼠心肌肥大信号通路的影响[J].第三军医大学学报,2006,28(3):223-226. 被引量:2
  • 2刘现忠,李相成,仲跻巍.肝脏再生信号机制研究进展[J].中华肝脏病杂志,2007,15(2):158-160. 被引量:4
  • 3Fausto N, Campbell J S, Riehle K J. Liver regeneration[J]. Hepatology, 2006, 43(2 Suppl 1): S45-S53.
  • 4Nadal C. Nonregenerative stimulation of hepatocyte proliferation in the rat: variable effects in relation to spontaneous liver growth; a possible link with metabolic induction [ J ]. Cell Prolif, 2000, 33 ( 5 ) : 287 - 300.
  • 5Chocian G, Zabielski P, Chabowski A. Liver regeneration after partial hepatectomy. Role of lipid mediators [ J]. Postepy Hig Med Dosw, 2002, 56(1) : 49-71.
  • 6Culjkovic B, Topisirovic I, Skrabanek L, et al. eIF4E is a central node of an RNA regulon that governs cellular proliferalion [ J ]. J Cell Biol, 2006, 175(3) : 415 -426.
  • 7Savinainen K J, Helenius M A, Lehtonen H J, et al. Overexpression of EIF3S3 promotes cancer cell growth [ J ]. Prostate, 2006, 66 ( 11 ) : 1144 - 1150.
  • 8Sharma N, Marguerat S, Mehta S, et al. The fission yeast Rpb4 subunit of RNA polymerase Ⅱ plays a specialized role in cell separation [J]. Mol Genet Genomics, 2006, 276(6) : 545 -554.
  • 9Ruchaud S, Carmena M, Earnshaw W C. Chromosomal passengers: conducting cell division[J]. Nat Rev Mol Cell Biol, 2007, 8 (10): 798 - 812.
  • 10Wittich S, Scherf H, Xie C, et al. Effect of inhibitors of histone deacetylase on the induction of cell differentiation in murine and hu- man erythroleukemia cell lines[J]. Anticancer Drugs, 2005, 16(6) : 635 - 643.

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