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BN52021对重症急性胰腺炎大鼠胰腺组织中核因子κB p65表达的影响

Effect of BN52021 on NFkappa-Bp65 expression in pancreatic tissues of rats with severe acute pancreatitis.

作者信息

Xia Shi-Hai, Fang Dian-Chun, Hu Chun-Xiu, Bi Hui-Ying, Yang Yin-Zhi, Di Yao

机构信息

Department of Gastroenterology, Southwest Hospital, Third Military Medical University, Chongqing 400038, China.

出版信息

World J Gastroenterol. 2007 Feb 14;13(6):882-8. doi: 10.3748/wjg.v13.i6.882.

Abstract

AIM

To investigate dynamic changes and significance of expression of NF-kappaBp65 in pancreatic tissues of rats with severe acute pancreatitis (SAP), as well as BN52021 effects.

METHODS

Wistar male rats were randomly divided into negative control group (NC group, n=60), SAP-model group (SAP group, n=60), and BN52021-treated group (BN group, n=60), and each of the above groups was respectively divided into 6 subgroups at different time points after operation (1 h, 2 h, 3 h, 6 h, 12 h, and 24 h) (n=10). By RT-PCR and Western blot, NF-kappaBp65 mRNA and its protein expression in pancreatic tissues of rats were detected respectively.

RESULTS

The expression of NF-kappaBp65 mRNA dynamically changed in both SAP groups and BN groups. The mRNA level was higher in SAP groups than NC groups at 2 h, 3 h, 12 h, and 24 h after operation (P<0.05), higher in BN groups than NC groups at all time points (P<0.05), and higher in BN groups than SAP group at 1 h (P<0.05). The NF-kappaBp65 protein level was higher in SAP groups than NC groups at 1 h, 3 h, and 6 h (P<0.01), and 2 h, 12 h, and 24 h (P<0.05), higher in BN groups than NC groups at all time points (P<0.05), and lower in BN groups than SAP groups at 1 h, 3 h, and 6 h (P<0.05).

CONCLUSION

The expression of NF-kappaBp65 in pancreatic tissues is dynamically changed and the changes play an important role in pathogenesis of SAP. BN52021 exerts therapeutic effects through reducing the expression level of NF-kappaBp65 protein in the early stage of SAP.

摘要

目的

探讨核因子-κB p65(NF-κB p65)在重症急性胰腺炎(SAP)大鼠胰腺组织中的表达动态变化及意义,以及BN52021的作用。

方法

将雄性Wistar大鼠随机分为阴性对照组(NC组,n = 60)、SAP模型组(SAP组,n = 60)和BN52021治疗组(BN组,n = 60),上述每组在术后不同时间点(1 h、2 h、3 h、6 h、12 h和24 h)再分别分为6个亚组(n = 10)。采用逆转录-聚合酶链反应(RT-PCR)和蛋白质免疫印迹法(Western blot)分别检测大鼠胰腺组织中NF-κB p65 mRNA及其蛋白表达。

结果

NF-κB p65 mRNA在SAP组和BN组中均呈动态变化。术后2 h、3 h、12 h和24 h,SAP组mRNA水平高于NC组(P < 0.05);各时间点BN组均高于NC组(P < 0.05);术后1 h,BN组高于SAP组(P < 0.05)。NF-κB p65蛋白水平在术后1 h、3 h和6 h,SAP组高于NC组(P < 0.01),2 h、12 h和24 h,SAP组高于NC组(P < 0.05);各时间点BN组均高于NC组(P < 0.05);术后1 h、3 h和6 h BN组低于SAP组(P < 0.05)。

结论

胰腺组织中NF-κB p65表达呈动态变化,且该变化在SAP发病机制中起重要作用。BN52021通过降低SAP早期NF-κB p65蛋白表达水平发挥治疗作用。

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本文引用的文献

1
Immune status and inflammatory response differ locally and systemically in severe acute pancreatitis.
Scand J Gastroenterol. 2006 Apr;41(4):472-80. doi: 10.1080/00365520500318965.
2
Role of platelet-activating factor in the pathogenesis of acute pancreatitis.
World J Gastroenterol. 2006 Jan 28;12(4):539-45. doi: 10.3748/wjg.v12.i4.539.
4
Proinflammatory effects of pancreatic elastase are mediated through TLR4 and NF-kappaB.
Biochem Biophys Res Commun. 2004 Oct 8;323(1):192-6. doi: 10.1016/j.bbrc.2004.08.077.
5
Metallothionein mediates the level and activity of nuclear factor kappa B in murine fibroblasts.
J Pharmacol Exp Ther. 2004 Aug;310(2):589-98. doi: 10.1124/jpet.104.066126. Epub 2004 Mar 23.
6
Systemic nf-kappaB activation in a transgenic mouse model of acute pancreatitis.
J Surg Res. 2003 Mar;110(1):310-4. doi: 10.1016/s0022-4804(03)00024-6.
8
10
NF-kappaB: a key role in inflammatory diseases.
J Clin Invest. 2001 Jan;107(1):7-11. doi: 10.1172/JCI11830.

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