Suppr超能文献

肿瘤坏死因子-α和血管内皮生长因子在门静脉高压大鼠食管中的表达。

Expression of TNF-alpha and VEGF in the esophagus of portal hypertensive rats.

作者信息

Yin Zhao-Hui, Liu Xun-Yang, Huang Rang-Lang, Ren Shu-Ping

机构信息

Division of Transplantation Surgery, Center for Surgical Sciences, Karolinska University Hospital, Huddinge B56, S-141 86 Stockholm, Sweden.

出版信息

World J Gastroenterol. 2005 Feb 28;11(8):1232-6. doi: 10.3748/wjg.v11.i8.1232.

Abstract

AIM

To investigate the expression of tumor necrosis factor-alpha (TNF-alpha) and vascular endothelial growth factor (VEGF) in the development of esophageal varices in portal hypertensive rats.

METHODS

Thirty male Sprague-Dawley (SD) rats in the model group in which a two-stage ligation of portal vein plus ligation of the left adrenal vein was performed, were divided into three subgroups (M(7), M(14), and M(21)) in which the rats were kiued on the seventh day, the 14(th) d and the 21 d after the complete portal ligation. Thirty male SD rats, which underwent the sham operation in the control group, were also separated into three subgroups (C(7), C(14) and C(21)) corresponding to the models. The expression of TNF-alpha and VEGF in the esophagus of all the six subgroups of rats were measured with immunohistochemical SP technique.

RESULTS

The portal pressure in the three model subgroups was significantly higher than that in the corresponding control subgroups (23.82+/-1.83 vs 11.61+/-0.86 cmH(2)O, 20.90+/-3.27 vs 11.43+/-1.55 cmH(2)O and 20.68+/-2.27 vs 11.87+/-0.79 cmH(2)O respectively, P<0.01), as well as the number (9.3+/-1.6 vs 5.1+/-0.8, 11.1+/-0.8 vs 5.4+/-1.3 and 11.7+/-1.5 vs 5.2+/-1.1 respectively, P<0.01) and the total vascular area (78 972.6+/-3 527.8 vs 12 993.5+/-4 994.8 mum(2), 107 207.5+/-4 6461.4 vs 11 862.6+/-5 423.2 mum(2) and 110 241.4+/-49 262.2 vs 11 973.7+/-3 968.5 mum(2) respectively, P<0.01) of submucosal veins in esophagus. Compared to the corresponding controls, the expression of TNF-alpha and VEGF in M(21) was significantly higher (2.23+/-0.30 vs 1.13+/-0.28 and 1.65+/-0.38 vs 0.56+/-0.30 for TNF-alpha and VEGF respectively, P<0.01), whereas there was no difference in M(7) (1.14+/-0.38 vs 1.06+/-0.27 and 0.67+/-0.35 vs 0.50+/-0.24 for TNF-alpha and VEGF respectively, P>0.05) and M(14) (1.20+/-0.25 vs 1.04+/-0.26 and 0.65+/-0.18 vs 0.53+/-0.25 for TNF-alpha and VEGF respectively, P>0.05). And the expression of TNF-alpha and VEGF in M(21) was significantly higher than that in M(7) (2.23+/-0.30 vs 1.14+/-0.38 and 1.65+/-0.38 vs 0.67+/-0.35 for TNF-alpha and VEGF respectively, P<0.01) and M(14) (2.23+/-0.30 vs 1.20+/-0.25 and 1.65+/-0.38 vs 0.65+/-0.18 for TNF-alpha and VEGF respectively, P<0.01), but there was no difference between M(7) and M(14) (1.14+/-0.38 vs 1.20+/-0.25 and 0.67+/-0.35 vs 0.65+/-0.18 for TNF-alpha and VEGF respectively, P>0.05).

CONCLUSION

In the development of esophageal varices in portal hypertensive rats, increased TNF-alpha and VEGF may be not an early event, and probably play a role in weakening the esophageal wall and the rupture of esophageal varices.

摘要

目的

探讨肿瘤坏死因子-α(TNF-α)和血管内皮生长因子(VEGF)在门静脉高压大鼠食管静脉曲张形成过程中的表达情况。

方法

将30只雄性Sprague-Dawley(SD)大鼠作为模型组,行门静脉两阶段结扎加左肾上腺静脉结扎术,术后将其分为三个亚组(M(7)、M(14)和M(21)),分别于门静脉完全结扎后第7天、第14天和第21天处死大鼠。30只接受假手术的雄性SD大鼠作为对照组,同样分为与模型组对应的三个亚组(C(7)、C(14)和C(21))。采用免疫组织化学SP法检测所有六个亚组大鼠食管中TNF-α和VEGF的表达。

结果

三个模型亚组的门静脉压力均显著高于相应对照组(分别为23.82±1.83 vs 11.61±0.86 cmH₂O、20.90±3.27 vs 11.43±1.55 cmH₂O和20.68±2.27 vs 11.87±0.79 cmH₂O,P<0.01),食管黏膜下静脉数量(分别为9.3±1.6 vs 5.1±0.8、11.1±0.8 vs 5.4±1.3和11.7±1.5 vs 5.2±1.1,P<0.01)及总面积(分别为78972.6±3527.8 vs 12993.5±4994.8 μm²、107207.5±46461.4 vs 11862.6±5423.2 μm²和110241.4±49262.2 vs 11973.7±3968.5 μm²,P<0.01)也显著高于对照组。与相应对照组相比,M(21)中TNF-α和VEGF的表达显著升高(TNF-α分别为2.23±0.30 vs 1.13±0.28,VEGF分别为1.65±0.38 vs 0.56±0.30,P<0.01),而M(7)(TNF-α分别为1.14±0.38 vs 1.06±0.27,VEGF分别为0.67±0.35 vs 0.50±0.24,P>0.05)和M(14)(TNF-α分别为1.20±0.25 vs 1.04±0.26,VEGF分别为0.65±0.18 vs 0.53±0.25,P>0.05)中无差异。且M(21)中TNF-α和VEGF的表达显著高于M(7)(TNF-α分别为2.23±0.30 vs 1.14±0.38,VEGF分别为t1.65±0.38 vs 0.67±0.3

相似文献

1
Expression of TNF-alpha and VEGF in the esophagus of portal hypertensive rats.
World J Gastroenterol. 2005 Feb 28;11(8):1232-6. doi: 10.3748/wjg.v11.i8.1232.
2
3
A rat model of esophageal varices.
Hepatology. 1991 Feb;13(2):353-8.
7
Antioxidant properties of glutamine and its role in VEGF-Akt pathways in portal hypertension gastropathy.
World J Gastroenterol. 2013 Jul 28;19(28):4464-74. doi: 10.3748/wjg.v19.i28.4464.
8
Early propranolol administration does not prevent development of esophageal varices in cirrhotic rats.
Eur Surg Res. 2009;42(1):11-6. doi: 10.1159/000166165. Epub 2008 Oct 30.
9
[Angioarchitecture of the lower esophagus in portal hypertension].
Nihon Shokakibyo Gakkai Zasshi. 1991 Jun;88(6):1336-40.
10
A rat model of liver cirrhosis and esophageal varices.
Res Exp Med (Berl). 2001 Mar;200(3):137-54.

本文引用的文献

2
The role of apoptosis-inducing receptors of the tumor necrosis factor family in thyroid cancer.
J Endocrinol. 2003 Aug;178(2):205-16. doi: 10.1677/joe.0.1780205.
4
The biology of VEGF and its receptors.
Nat Med. 2003 Jun;9(6):669-76. doi: 10.1038/nm0603-669.
6
Nitric oxide synthase distribution in esophageal mucosa and hemodynamic changes in rats with cirrhosis.
World J Gastroenterol. 1999 Jun;5(3):213-216. doi: 10.3748/wjg.v5.i3.213.
7
Immunohistochemical localization of vascular endothelial growth factor in the rat portal hypertensive gastropathy.
J Gastroenterol Hepatol. 2001 Apr;16(4):429-37. doi: 10.1046/j.1440-1746.2001.02452.x.
9
The role of tumor necrosis factor in the pathophysiology of heart failure.
J Am Coll Cardiol. 2000 Mar 1;35(3):537-44. doi: 10.1016/s0735-1097(99)00600-2.
10
Role of vascular endothelial growth factor in portal hypertensive gastropathy.
Digestion. 2000;61(2):98-106. doi: 10.1159/000007741.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验