Iwai Tomohisa, Ichikawa Takafumi, Goso Yukinobu, Ikezawa Tomoaki, Saegusa Yoichi, Okayasu Isao, Saigenji Katsunori, Ishihara Kazuhiko
Department of Gastroenterology, Kitasato University School of Medicine, Sagamihara, Japan.
J Gastroenterol. 2009;44(4):277-84. doi: 10.1007/s00535-009-0007-0. Epub 2009 Mar 13.
The luminal surface of the gastrointestinal tract is covered by a viscoelastic gel layer that acts as a protective barrier against the intraluminal environment. Because the situation of the small intestine has not been elucidated to the same degree as other sections, in this study, we investigated the effects of indomethacin on the rat small intestinal mucosa.
Male Wistar rats were given indomethacin 10 mg/kg s-c and sacrificed 1, 3, 7, or 14 days later. The small intestine was opened along the anti-mesenteric side, and examined macroscopically. Total mucin content in the small intestinal epithelium was measured and immunoreactivity was examined using anti-mucin monoclonal antibodies HCM31 and PGM34.
Indomethacin caused punched out and linear ulcers located mostly along the mesenteric margin of the distal jejunum with sparing of the ileum. Histological examination showed sialomucin recognized by HCM31 increased on day 3 especially in the regenerating epithelium around the ulcer edge. Furthermore, the surface mucous gel layer displayed a multilaminated pattern, consisting of non-sulfated sialomucin-rich layers and sulfated mucin-rich layers, where both mucins had the common core protein, MUC2. Biochemical measurements also showed the total mucin content of the jejunum increased transiently and HCM31-positive mucin increased approximately 4 times greater than baseline on day 3, but no marked changes were observed in the ileum, with few ulcers observed.
Indomethacin administration causes quantitative and qualitative change in jejunal mucin. In particular, sialomucin plays an important role in regenerating epithelium during the healing process following indomethacin-induced mucosal damage.
胃肠道的管腔表面覆盖着一层粘弹性凝胶层,该层作为抵御管腔内环境的保护屏障。由于小肠的情况尚未像其他部分那样得到同等程度的阐明,在本研究中,我们调查了吲哚美辛对大鼠小肠黏膜的影响。
给雄性Wistar大鼠皮下注射10mg/kg吲哚美辛,并在1、3、7或14天后处死。沿小肠的系膜对侧打开,进行宏观检查。测量小肠上皮中的总粘蛋白含量,并使用抗粘蛋白单克隆抗体HCM31和PGM34检测免疫反应性。
吲哚美辛导致主要沿空肠远端系膜缘出现穿孔性和线性溃疡,回肠未受累。组织学检查显示,HCM31识别的唾液酸粘蛋白在第3天增加,尤其是在溃疡边缘的再生上皮中。此外,表面粘液凝胶层呈现多层模式,由富含非硫酸化唾液酸粘蛋白的层和富含硫酸化粘蛋白的层组成,这两种粘蛋白都有共同的核心蛋白MUC2。生化测量还显示,空肠的总粘蛋白含量短暂增加,HCM31阳性粘蛋白在第3天比基线增加约4倍,但回肠未观察到明显变化,溃疡很少。
给予吲哚美辛会导致空肠粘蛋白发生定量和定性变化。特别是,唾液酸粘蛋白在吲哚美辛诱导的黏膜损伤后的愈合过程中,对再生上皮起着重要作用。