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NF-κB p65、Caspase-3在重症急性胰腺炎大鼠肝损伤中的表达意义 被引量:5

Role of NF-κB p65,Caspase-3 in the course of liver injury in rat with SAP
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摘要 目的探讨重症急性胰腺炎大鼠肝损伤中NF-κB p65、Caspase-3表达意义。方法将SD大鼠36只随机分成SAP组(n=18)、假手术组(n=18)。采用改良的Aho’s法制作SAP模型,并经病理及血清学检查证实成功的SAP模型,通过免疫组织化学方法动态观察2组大鼠肝组织中NF-κB p65、Caspase-3的表达,同时观察肝脏病理变化。结果病理观察显示,SAP组大鼠肝组织可见肝细胞明显肿胀、肝窦充血,肝细胞界限不清,肝索扭曲,至12h可见局灶性坏死,并有大量中性粒细胞及淋巴细胞浸润,以小叶区明显。免疫组化检测结果显示在SAP组肝组织中3h、6h、12hNF-κB p65表达分别为(2.83±1.84)、(5.50±1.98)、(8.00±1.55),Caspase-3表达分别为(2.50±0.84)、(5.34±1.16)、(6.17±1.61),其12h与3h比较均有统计学意义(P<0.05);假手术组呈弱阳性表达,并随时间延长阳性表达比较无统计学意义(P>0.05)。不同组别肝脏组织镜下评分、肝组织NF-κB P65及Caspase-3表达经Pearson相关性分析三者成正相关性(P<0.05)。结论NF-κB、Caspase-3升高为SAP肝损伤早期表现,其过度表达在SAP肝脏损伤发病机制中可能发挥重要作用。 Objective To study the role of NF-κB p65,Caspase-3 in the course of liver injury in rat with severe acute pancre- atitis(SAP).Methods A total of 36 Spragne Dawley rats were randomly and averagely divided into 2 groups, named group A , group C.A and C severed as SAP model and sham operation group, respectively. The modified Aho's method was used to reproduce SAP models, and the success of SAP model confirmed by pathology and serum examination,the expression of NF-κB p65,Caspase-3 in liver tissues was determined by immunohistochemical staining and pathological changes in liver were observed.Results The histological examination revealed obviously edema, congestive in hepatic sinusoid, nuclear psychosis, liver cells boundaries unclear, and liver Faso distorted after modeling, Focal necrosis can be seen and a large number of neutrophil and lymphocyte infiltrate in the lobular ar eas at 12h after modeling, In group Aand C, the expression of NF-κB p65 were(2.83±1.84vs2.67±0.52), (5.50±1.98vs2.17±0.75)and (8.00+1.55vs2.00±1.10)at the 3rd ,6th ,12th hour, respectively, while in the expression of Caspase-3 were (2.50±0.84vs 2.17±0.75), (5.34±1.16vs3.17±0.65), (6.17±1.61vs3.33±1.37)in the same time, respectively, there were significant difference between group A and C at the 12th and 3rd hour (P〈0.05). Conclusion The increased expression of NF-κB p65 and Caspase-3 were early performance on liver injury in rats with SAP,and the over expressions of them play a pivotal role in the pathogenesis of SAP complicated with liver injury.
出处 《江西医药》 CAS 2009年第11期1069-1072,共4页 Jiangxi Medical Journal
关键词 重症急性胰腺炎 肝损伤 NF—κB P65 CASPASE-3 severe acute pancreatitis liver injury NF-κB P65 Caspase-3
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  • 1姜景平 徐萍 陈令全 等.p38MAPK信号通路在重症急性胰腺炎大鼠发病机制中的作用[J].中华胰腺病杂志,2008,8(4):249-249.
  • 2Camargo CA Jr, Madden JF,Gao W,et al. interleukln- 6 Protects liver against waxm ischemia/reperfusion injury and promotes hepatocyte proliferation in the rodent.HePatology,1997,26(6):1513.
  • 3Brasier AR. The NF-kappaB regulatory network ,Cardiovasc Toxicol, 2006,6(2):111.
  • 4Nagase H,Fukuyama H,Tanaka M,et al.Mutually regulated expression of easpase-activated DNase and its inhibitor for apoptotie DNA fragmentation.Cell Death and Differentiation,2003,10:142.
  • 5Gruenbaum Y,Goldman RD,Meyuhas R,et al.The nuclear lamina and its functions in the nucleus.Int Rev Cytol.2003.226:1.
  • 6Endo S,Inoue Y,Fujino Y,et al.Soluble Fas and soluble Fas L levels in patients with acute pancreatitis.Research Communications in Molecular Pathology Pharmacology,2000,108:179.
  • 7Galagher SF,Yang J,Baksh K,et al. Acute pancreatitis induces FasL gene expression and apoptosis in the liver.J Surg Research,2004,22:201.
  • 8Yang J,Gallagher SF ,Haines K ,et al.Kupffer cell-derived Fas lig- and plays a role in liver injury and hepatocyte death.J Gastrointest Surg,2004,8:166.

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  • 2肖经纬,李斌,钟才高.肝细胞凋亡机制及其检测方法的研究进展[J].国外医学(卫生学分册),2006,33(2):93-96. 被引量:11
  • 3高建芝,徐自超,王庆志,王辉.核因子-κB与感染性休克大鼠肝细胞凋亡的关系[J].新乡医学院学报,2007,24(5):447-450. 被引量:13
  • 4Brasier AR. The NF-kappaB regulatory network[J]. Cardiovasc Toxic- ol,2006,6(2): !. 11 - 130.
  • 5Zhao Z, Yang P, Eekert RL. Caspase-8:a key role in the pathogenesis of diabetic embryopathy[J]. Birth Defects Res 8 Dev Repmd Toxicol, 2009,86(1):72-77.
  • 6Boenenmn K, Mei BC, Detmis AM, et al. Sensing easpase 3 activity with quantum clot-fluorescent protein assemblies[J]. J Am Chem Soc, 2009,131(11):3828-3829.
  • 7Li J, Yuan J. Caspases in apoptosis and beyond [J]. Oncogene, 2008,27 (48):6194-6206.
  • 8Nagase H. Fukuyama H, Tanaka M, et al. Mutually regulated expression of caspase-activated DNase an d its inhibitor fbr apoptotic DNA fragmentation[J]. Cell Death and Differentiation,2003,10:142.
  • 9Li YY,Gao ZF. Acute pancreatitif and NF-K B[J]. World Chinese Jou- rnal of Digestology,2001,9:420-421.
  • 10Tai DI, Tsai SL. Activation of nuclear factor K B in hepatitis C virus infection:implication for pathogenesis and hepatoearcinogenesis [J]. Hepatology, 2000,31(12):656-658.

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