Lazaratos S, Kashimura H, Nakahara A, Fukutomi H, Osuga T, Urushidani T, Miyauchi T, Goto K
Department of Internal Medicine, University of Tsukuba, Ibaraki, Japan.
Am J Physiol. 1993 Sep;265(3 Pt 1):G491-8. doi: 10.1152/ajpgi.1993.265.3.G491.
To investigate whether submucosally applied endothelin-1 (ET-1) can induce gastric ulcer, ET-1 (62.5, 125, 250, and 500 pmol/kg) was injected in the submucosal layer of the rat gastric body. Twenty-four hours later, gastric ulcer (ulcer area: 10.31 +/- 5.13 mm2, mean +/- SE, at 500 pmol/kg, n = 8) was induced. The mucosal damage induced by the two highest doses was present even at 2 wk after their injection. Measurement of the mucosal blood flow at the injected area with three different methods (laser-Doppler flowmetry, hydrogen gas clearance, and reflectance spectrophotometry) revealed that injected ET-1 produced an extremely long-lasting vasoconstriction. Pretreatment with nicardipine, a Ca(2+)-channel blocker (1 mg/kg iv), significantly attenuated the ET-1-induced mucosal damage as well as the decrease in mucosal blood flow. Pretreatment with omeprazole (5-40 mumol/kg) also, significantly attenuated the ET-1-induced mucosal damage. Combined pretreatment with omeprazole (40 mumol/kg) and nicardipine almost abolished the ET-1-induced damage. The present study shows that a novel model for experimental ulcers can be induced by submucosal injection of ET-1.
为研究黏膜下注射内皮素-1(ET-1)是否能诱发胃溃疡,将ET-1(62.5、125、250和500 pmol/kg)注射到大鼠胃体黏膜下层。24小时后,诱发了胃溃疡(500 pmol/kg时溃疡面积:10.31±5.13 mm²,平均值±标准误,n = 8)。即使在注射后2周,两种最高剂量诱发的黏膜损伤依然存在。用三种不同方法(激光多普勒血流仪、氢气清除法和反射分光光度法)测量注射部位的黏膜血流量,结果显示注射ET-1可产生极其持久的血管收缩。用钙通道阻滞剂尼卡地平(1 mg/kg静脉注射)预处理可显著减轻ET-1诱发的黏膜损伤以及黏膜血流量的减少。用奥美拉唑(5 - 40 μmol/kg)预处理也可显著减轻ET-1诱发的黏膜损伤。奥美拉唑(40 μmol/kg)和尼卡地平联合预处理几乎可消除ET-1诱发的损伤。本研究表明,黏膜下注射ET-1可诱发一种新型实验性溃疡模型。