Ichikawa T, Ishihara K, Kusakabe T, Kawakami T, Hotta K
Department of Biochemistry, Kitasato University School of Medicine, Sagamihara, Kanagawa, Japan.
Life Sci. 1999;65(4):PL41-6. doi: 10.1016/s0024-3205(99)00266-0.
Although the involvement of nitric oxide (NO) in an increasing gastric mucus metabolism has been reported, information on whether or not its activation is limited to the specific mucus-producing cells is lacking. In this paper, we report the effect of the exogenous NO-donor, isosorbide dinitrate (ISDN), and second-generation histamine H2 receptor antagonist roxatidine (2-acetoxy-N-(3-[m-(1-piperidinylmethyl)phenoxy]propyl)acetamide hydrochloride) which is demonstrated to accelerate the mucin metabolism mediated by endogenous NO, on the mucin biosynthesis in distinct sites and layers of the rat gastric mucosa using an organ culture technique. Radiolabeled mucin was obtained from the tissue of full-thickness and the deep corpus layer, and the antrum of the rat stomach incubated for 5 hr with [3H]glucosamine(GlcN) in vitro. With the addition of ISDN to the culture medium, 3H-labeled mucin in the full-thickness corpus mucosa increased to 124-145% of the control (p<0.05), but not in the antrum. This stimulation of the mucin synthesis disappeared by the removal treatment of the surface mucous cell layer which has immunoreactivity of neuronal NO synthase. Similarly, roxatidine stimulated the mucin biosynthesis in the full-thickness corpus mucosa, but not in the gland mucous cell layer. These results suggest that the stimulation of the mucin biosynthesis mediated by NO is restricted to the surface mucous cells of the rat gastric oxyntic mucosa.
尽管已有报道称一氧化氮(NO)参与了胃黏液代谢的增加,但关于其激活是否仅限于特定的黏液分泌细胞的信息尚缺乏。在本文中,我们报告了外源性NO供体硝酸异山梨酯(ISDN)和第二代组胺H2受体拮抗剂罗沙替丁(2-乙酰氧基-N-(3-[间-(1-哌啶基甲基)苯氧基]丙基)乙酰胺盐酸盐)对大鼠胃黏膜不同部位和层黏蛋白生物合成的影响,该拮抗剂已被证明可加速内源性NO介导的黏蛋白代谢,采用器官培养技术进行研究。放射性标记的黏蛋白是从大鼠胃全层和深层胃体组织以及胃窦组织中获得的,这些组织在体外与[3H]葡糖胺(GlcN)孵育5小时。向培养基中添加ISDN后,胃体全层黏膜中3H标记的黏蛋白增加至对照的124 - 145%(p<0.05),但胃窦中未增加。通过去除具有神经元型一氧化氮合酶免疫反应性的表面黏液细胞层的处理,这种对黏蛋白合成的刺激消失。同样,罗沙替丁刺激了胃体全层黏膜中的黏蛋白生物合成,但在腺黏液细胞层中未刺激。这些结果表明,由NO介导的黏蛋白生物合成刺激仅限于大鼠胃泌酸黏膜的表面黏液细胞。