Role of nuclear factor kappaB in intestine injury induced by hepatic ischemia reperfusion

Chen Junhua , Wang Guobin

Current Medical Science ›› 2004, Vol. 24 ›› Issue (26) : 284 -285.

PDF
Current Medical Science ›› 2004, Vol. 24 ›› Issue (26) : 284 -285. DOI: 10.1007/BF02832014
Article

Role of nuclear factor kappaB in intestine injury induced by hepatic ischemia reperfusion

Author information +
History +
PDF

Abstract

The role of nuclear factor kappaB in intestine injury induced by hepatic ischemia reperfusion was investigated. Eighteen male Wistar rats were divided into 3 groups randomly: sham operation group (group A), hepatic ischemia reperfusion group (group B) and hepatic ischemia reperfusion plus pyrrolidine dithiocarbamate (PDTC) group (group C). The rats in group A were only subjected to laparotomy, those in group B underwent partial hepatic ischemia reperfusion (ischemia for 1 h and reperfusion for 2 h) and those in group C underwent the same procedure as that of group B but received PDTC 200 mg/kg i. v. before and after ischemia. After reperfusion, tissues of jejunum and venous blood were obtained for measurement of TNF-α, MDA and MPO. The levels of TNF-α in jejunum and venous blood, the levels of MPO in jejunum in group B were significantly higher than those in group A and group C (P<0.05). There was no significant different in the levels of MDA between group B and group C. The severity of histological intestinal injury in group B and group C was similar. Hepatic ischemia reperfusion caused intestine injury, NF-kappaB may play an important role in this course and the targeting of upstream components of the inflammatory response, such as NF-kappaB, may have important therapeutic applications.

Keywords

liver / ischemia reperfusion / nuclear factor kappaB / rats

Cite this article

Download citation ▾
Chen Junhua, Wang Guobin. Role of nuclear factor kappaB in intestine injury induced by hepatic ischemia reperfusion. Current Medical Science, 2004, 24(26): 284-285 DOI:10.1007/BF02832014

登录浏览全文

4963

注册一个新账户 忘记密码

References

[1]

LiuD L, JeppssonB, HakanssonC H, et al. . Multiplesystem organ damage resulting from prolonged hepatic flow interruption. Arch Surg, 1996, 131442-442

[2]

GhoshS, MayM J, KoppE B, et al. . Rel proteins: evolutionarily conserved mediators of immune responses. Annu Rev Immunol, 1998, 16225-225

[3]

KobayashiH, NonamiT, KurokawaT, et al. . Mechanism and prevention of ischemia reperfusion induced liver injury in rats. J Surg Res, 1991, 51240-240

[4]

LentschA B, YoshidomeH, CheadleW G, et al. . Chemokine involvement in hepatic ischemia reperfusion injury in mice: roles for macrophage inflammatory protein 2 and KC. Hepatology, 1998, 271172-1172

[5]

PeraltaC, FernandezL, PanesJ, et al. . Preconditioning protects against systemic disorders associated with hepatic ischemia reperfusion through blockade of tumor necrosis factor-α induced P-selectin up-regulation in the rat. Hepatology, 2001, 33100-100

[6]

CollinsT, ReadM A, NeishA S, et al. . Transcriptional regulation of endothelial cell adhesion molecules: NF-κB and cytokine-inducible enhancers. FASEBJ, 1995, 9899-899

[7]

ZwackaR M, ZhangY, ZhouW, et al. . Ischemia reperfusion injury in the liver of BALB/c mice activates AP-1 and nuclear factorκB independently of IkB degradation. Hepatology, 1998, 281022-1022

[8]

Van AntwarpD J, MartinS J, VermaI M, et al. . Inhibition of TNF induced apoptosis by NF-κB. Trends Cell Biol, 1998, 8107-107

AI Summary AI Mindmap
PDF

73

Accesses

0

Citation

Detail

Sections
Recommended

AI思维导图

/