Okuda Tomoyuki, Azuma Takeshi, Ohtani Masahiro, Masaki Ryuho, Ito Yoshiyuki, Yamazaki Yukinao, Ito Shigeji, Kuriyama Masaru
Second Department of Internal Medicine, Faculty of Medical Sciences, University of Fukui, Matsuoka-cho, Yoshida-gun, Fukui 9101193, Japan.
World J Gastroenterol. 2005 Mar 14;11(10):1535-9. doi: 10.3748/wjg.v11.i10.1535.
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).
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.
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.
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.
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。
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。
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。
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。