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吲哚美辛而非幽门螺杆菌可抑制离体豚鼠胃的适应性舒张。

Indomethacin, but not Helicobacter pylori, inhibits adaptive relaxation in isolated guinea-pig stomach.

作者信息

Higuchi K, Tominaga K, Watanabe T, Uno H, Shiba M, Sasaki E, Tanigawa T, Takashima T, Hamaguchi M, Oshitani N, Matsumoto T, Iwanaga Y, Fukuda T, Fujiwara Y, Arakawa T

机构信息

Department of Gastroenterology, Graduate School of Medicine, Osaka City University, Osaka, Japan.

出版信息

Drugs Exp Clin Res. 2004;30(5-6):235-41.

Abstract

Nonsteroidal anti-inflammatory drugs (NSAIDs) and Helicobacter pylori (H. pylori) are major factors in gastritis and peptic ulcer However, the role of NSAIDs and H. pylori infection in dyspepsia remains unclear. Gastric adaptive relaxation may be related to the pathogenesis of functional dyspepsia because the response is often disturbed in dyspeptic patients. In this study, we investigated the effects of indomethacin or H. pylori water extracts on gastric adaptive relaxation. This experiment was performed using the modified method of Desai et al. Isolated guinea-pig stomach in an organ bath was monitored for intragastric pressure and volume. Adaptive relaxation was induced by gastric luminal distention. The effects of indomethacin and H. pylori on gastric relaxation were tested in this system. Indomethacin (> 1 x 10(-5) M) significantly inhibited adaptive relaxation. Indomethacin (> 3 x 10(-6) M) induced gastric relaxation in a dose-dependent fashion. However, aspirin at a concentration sufficient for cyclooxygenase (COX)-1 inhibition did not induce gastric relaxation. Preincubation with N-nitro-L-arginine methyl ester, a nitric oxide (NO)-synthase inhibitor, inhibited indomethacin-induced gastric relaxation. Adaptive relaxation was not affected by H. pylori water extracts. In conclusion, indomethacin inhibited adaptive relaxation via prior gastric relaxation. NO production, but not COX-1 inhibition, may be involved in this effect of indomethacin. H. pylori water extracts may not have direct effects on adaptive relaxation. Inhibition of adaptive relaxation may be one of the major mechanisms underlying NSAID-induced dyspepsia.

摘要

非甾体抗炎药(NSAIDs)和幽门螺杆菌(H. pylori)是胃炎和消化性溃疡的主要因素。然而,NSAIDs和幽门螺杆菌感染在消化不良中的作用仍不明确。胃适应性舒张可能与功能性消化不良的发病机制有关,因为在消化不良患者中这种反应常常受到干扰。在本研究中,我们研究了吲哚美辛或幽门螺杆菌水提取物对胃适应性舒张的影响。本实验采用了Desai等人改进的方法。在器官浴中分离的豚鼠胃监测胃内压和容积。通过胃腔内扩张诱导适应性舒张。在该系统中测试了吲哚美辛和幽门螺杆菌对胃舒张的影响。吲哚美辛(>1×10^(-5) M)显著抑制适应性舒张。吲哚美辛(>3×10^(-6) M)以剂量依赖性方式诱导胃舒张。然而,足以抑制环氧化酶(COX)-1的阿司匹林浓度并未诱导胃舒张。用一氧化氮(NO)合酶抑制剂N-硝基-L-精氨酸甲酯预孵育可抑制吲哚美辛诱导的胃舒张。适应性舒张不受幽门螺杆菌水提取物的影响。总之,吲哚美辛通过先诱导胃舒张来抑制适应性舒张。NO生成而非COX-1抑制可能参与吲哚美辛的这种作用。幽门螺杆菌水提取物可能对适应性舒张没有直接影响。抑制适应性舒张可能是NSAID诱导的消化不良的主要机制之一。

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