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新型抗炎药物安吡昔康对大鼠的胃保护作用:一氧化氮的参与

Gastrosparing effect of new antiinflammatory drug amtolmetin guacyl in the rat: involvement of nitric oxide.

作者信息

Pisano C, Grandi D, Morini G, Coppelli G, Vesci L, Lo Giudice P, Pace S, Pacifici L, Longo A, Coruzzi G, Carminati P

机构信息

Research and Development, Sigma-Tau, Pomezia, Roma, Italy.

出版信息

Dig Dis Sci. 1999 Apr;44(4):713-24. doi: 10.1023/a:1026653623516.

Abstract

The effect of the nonsteroidal antiinflammatory drug (NSAID) amtolmetin guacyl (AMG) on the gastric mucosa was studied in the rat by means of histological and functional techniques. AMG administered at 50-300 mg/kg intragastrically was virtually devoid of gastrolesive properties after either acute or repeated treatment. By contrast, its metabolite, tolmetin (TOL, 15-60 mg/kg, intragastrically) caused dose-dependent gastric damage after both treatments. Light and electron microscopy revealed that AMG induced minimal changes in the surface epithelium layer, without signs of vasocongestion or leukocytes adherence. AMG (50 mg/kg intragastrically) did not change basal gastric potential difference (PD), whereas acetylsalicylic acid and ibuprofen induced falls in PD of 22 and 27 mV, respectively. AMG (50 mg/kg intragastrically) reduced by 60% the fall in PD induced by 50% ethanol; this inhibition was dependent on the incubation time, and was maximal when AMG was given 4 hr before ethanol. AMG (100 mg/kg intragastrically) induced an increase in NO synthase type 2 (NOS2) activity, which was significantly different from control values, when AMG was administered 4 hr before the test. The metabolites of AMG, tolmetin, MED 5, and guaiacol were ineffective. Pharmacokinetic analysis of the residence time of AMG in the different areas of the gastrointestinal tract, revealed that AMG remains in the gastrointestinal tract at least for 4 hr, the time necessary for a maximal induction of NOS2 and for maximal protection against ethanol-induced damage. In conclusion, these data indicate that the nonsteroidal antiinflammatory drug amtolmetin guacyl is devoid of gastrolesive properties; this gastro-sparing effect seems to involve the production of nitric oxide, which can counteract the damaging effects due to prostaglandin inhibition. The presence in the stomach of the native molecule of amtolmetin guacyl seems to be necessary for the protective effect observed.

摘要

通过组织学和功能技术,在大鼠中研究了非甾体抗炎药安多美汀瓜西酯(AMG)对胃黏膜的影响。胃内给予50 - 300mg/kg的AMG,无论是急性还是重复给药后,几乎都没有胃损伤特性。相比之下,其代谢产物托美汀(TOL,15 - 60mg/kg,胃内给药)在两种给药方式后均引起剂量依赖性胃损伤。光镜和电镜显示,AMG引起表面上皮层的变化极小,无血管充血或白细胞黏附迹象。AMG(胃内给药50mg/kg)未改变基础胃电位差(PD),而乙酰水杨酸和布洛芬分别使PD下降22mV和27mV。AMG(胃内给药50mg/kg)使50%乙醇诱导的PD下降减少了60%;这种抑制作用取决于孵育时间,在乙醇给药前4小时给予AMG时抑制作用最大。AMG(胃内给药100mg/kg)在试验前4小时给药时,诱导2型一氧化氮合酶(NOS2)活性增加,与对照值有显著差异。AMG的代谢产物托美汀、MED 5和愈创木酚无效。对AMG在胃肠道不同区域停留时间的药代动力学分析表明,AMG在胃肠道中至少停留4小时,这是最大程度诱导NOS2和最大程度保护免受乙醇诱导损伤所需的时间。总之,这些数据表明非甾体抗炎药安多美汀瓜西酯没有胃损伤特性;这种胃保护作用似乎涉及一氧化氮的产生,它可以抵消由于前列腺素抑制引起的损伤作用。安多美汀瓜西酯天然分子在胃中的存在似乎是观察到保护作用所必需的。

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