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缺氧诱导因子1α和血管内皮生长因子在缺血性结肠炎中的过表达

Hypoxia-inducible factor 1 alpha and vascular endothelial growth factor overexpression in ischemic colitis.

作者信息

Okuda Tomoyuki, Azuma Takeshi, Ohtani Masahiro, Masaki Ryuho, Ito Yoshiyuki, Yamazaki Yukinao, Ito Shigeji, Kuriyama Masaru

机构信息

Second Department of Internal Medicine, Faculty of Medical Sciences, University of Fukui, Matsuoka-cho, Yoshida-gun, Fukui 9101193, Japan.

出版信息

World J Gastroenterol. 2005 Mar 14;11(10):1535-9. doi: 10.3748/wjg.v11.i10.1535.

Abstract

AIM

To examine the etiology and pathophysiology in human ischemic colitis from the viewpoint of ischemic factors such as hypoxia-inducible factor 1 alpha (HIF-1 alpha and vascular endothelial growth factor (VEGF).

METHODS

Thirteen patients with ischemic colitis and 21 normal controls underwent colonoscopy. The follow-up colonoscopy was performed in 8 patients at 7 to 10 d after the occurrence of ischemic colitis. Biopsy samples were subjected to real-time RT-PCR and immunohistochemistry to detect the expression of HIF-1 alpha and VEGF.

RESULTS

HIF-1 alpha and VEGF expression were found in the normal colon tissues by RT-PCR and immunohistochemistry. HIF-1 alpha and VEGF were overexpressed in the lesions of ischemic colitis. Overexpressed HIF-1 alpha and VEGF RNA quickly decreased to the normal level in the scar regions at 7 to 10 d after the occurrence of ischemic colitis.

CONCLUSION

Constant expression of HIF-1 alpha and VEGF in normal human colon tissue suggested that HIF-1 alpha and VEGF play an important role in maintaining tissue integrity. We confirmed the ischemic crisis in ischemic colitis at the molecular level, demonstrating overexpression of HIF-1 alpha and VEGF in ischemic lesions. These ischemic factors may play an important role in the pathophysiology of ischemic colitis.

摘要

目的

从缺氧诱导因子1α(HIF-1α)和血管内皮生长因子(VEGF)等缺血因素的角度,研究人类缺血性结肠炎的病因和病理生理学。

方法

13例缺血性结肠炎患者和21例正常对照者接受结肠镜检查。8例缺血性结肠炎患者在发病后7至10天进行了随访结肠镜检查。对活检样本进行实时逆转录聚合酶链反应(RT-PCR)和免疫组织化学检测,以检测HIF-1α和VEGF的表达。

结果

通过RT-PCR和免疫组织化学在正常结肠组织中发现了HIF-1α和VEGF表达。HIF-1α和VEGF在缺血性结肠炎病变中过度表达。缺血性结肠炎发病后7至10天,过度表达的HIF-1α和VEGF RNA在瘢痕区域迅速降至正常水平。

结论

HIF-1α和VEGF在正常人体结肠组织中的持续表达表明,HIF-1α和VEGF在维持组织完整性方面发挥着重要作用。我们在分子水平上证实了缺血性结肠炎中的缺血危机,表明HIF-1α和VEGF在缺血性病变中过度表达。这些缺血因素可能在缺血性结肠炎的病理生理学中发挥重要作用。

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