Mattsson H, Larsson H
Scand J Gastroenterol. 1987 May;22(4):491-8. doi: 10.3109/00365528708991496.
Regional blood flow in the gastrointestinal tract (forestomach, corpus, antrum, duodenum, jejunum, and colon) was determined in the conscious rat by means of the microsphere technique. The effects on blood flow were determined after omeprazole (orally and intravenously) and cimetidine (intravenously) during both basal and pentagastrin-stimulated gastric acid secretion. Under basal conditions neither omeprazole nor cimetidine decreased the blood flow in the gastrointestinal tract in spite of pronounced inhibition of acid secretion. On the contrary, there was a tendency towards an increased blood flow in the mucosal layer of the corpus after the oral (80 mumol/kg) and the high intravenous (10 mumol/kg) dose of omeprazole. When omeprazole was given intravenously to rats during pentagastrin-stimulated acid secretion, blood flow in the gastric mucosa was unaffected in spite of complete or almost complete inhibition of acid secretion. In contrast, cimetidine decreased the mucosal blood flow, indicating that the pentagastrin-induced increase in blood flow to some extent is mediated by H2 receptors.
采用微球技术测定清醒大鼠胃肠道(前胃、胃体、胃窦、十二指肠、空肠和结肠)的局部血流。在基础胃酸分泌和五肽胃泌素刺激的胃酸分泌过程中,分别经口和静脉给予奥美拉唑以及静脉给予西咪替丁后,测定其对血流的影响。在基础状态下,尽管胃酸分泌受到显著抑制,但奥美拉唑和西咪替丁均未降低胃肠道血流。相反,经口给予高剂量(80 μmol/kg)奥美拉唑和静脉给予高剂量(10 μmol/kg)奥美拉唑后,胃体黏膜层血流有增加趋势。在五肽胃泌素刺激胃酸分泌期间静脉给予奥美拉唑时,尽管胃酸分泌被完全或几乎完全抑制,但胃黏膜血流未受影响。相比之下,西咪替丁可降低黏膜血流,表明五肽胃泌素诱导的血流增加在一定程度上是由H2受体介导的。