Nishida K, Ohta Y, Ishiguro I
Department of Biochemistry, School of Medicine, Fujita Health University, Toyoake, Aichi, Japan.
Jpn J Pharmacol. 1998 Dec;78(4):519-22. doi: 10.1254/jjp.78.519.
We examined whether the increasing action of teprenone (TP) on mucus synthesis and content in rat gastric mucosa is related to nitric oxide (NO) formation via NO synthase (NOS) in the tissue. TP (200 mg/kg)-induced increases in levels of gastric mucosal hexosamine and adherent mucus were inhibited with decreased gastric mucosal NOS activity and nitrite/nitrate concentration by co-administration of NG-monomethyl L-arginine (100 mg/kg), a NOS inhibitor, but not its D-isomer. These results suggest that TP exerts an increasing action on gastric mucus synthesis and content possibly under the condition of maintained NO production via NOS in gastric mucosal tissues, although the precise mechanisms for the action of TP is still unclear.
我们研究了替普瑞酮(TP)对大鼠胃黏膜黏液合成及含量的增强作用是否与组织中通过一氧化氮合酶(NOS)生成一氧化氮(NO)有关。通过共同给予一氧化氮合酶抑制剂NG-单甲基-L-精氨酸(100mg/kg)而非其D-异构体,可抑制TP(200mg/kg)诱导的胃黏膜己糖胺水平和黏附性黏液增加,同时胃黏膜NOS活性及亚硝酸盐/硝酸盐浓度降低。这些结果表明,TP可能在胃黏膜组织中通过一氧化氮合酶维持一氧化氮生成的条件下,对胃黏液合成及含量发挥增强作用,尽管TP作用的确切机制仍不清楚。