Cho C H, Ogle C W
Eur J Pharmacol. 1979 Apr 1;55(1):23-33. doi: 10.1016/0014-2999(79)90144-4.
The effects of atropine, mepyramine, metiamide or NaHCO3 on gastric ulceration, gastric secretion and gastric mast cell degranulation were studied in stressed pylorus-occluded rats. The influence of dexamethasone pretreatment on stress ulcers in animals without pylorus occlusion (intact rats) was also examined. Stress produced a high glandular lesion incidence and ulcer index, and markedly lowered gastric secretion and glandular wall mast cell counts. Injected 0.5 h before stress, atropine, mepyramine or metiamide strongly antagonised ulceration. Atropine or metiamide, but not mepyramine, reduced gastric secretion. Only atropine prevented stress-induced mast cell changes. NaHCO3, given intragastrically before stress, did not prevent ulceration or mast cell degranulation despite complete neutralisation of gastric acid. Dexamethasone-induced gastric mucosal mast cell depletion could reduce stress ulceration. The findings show that stress degranulates stomach mast cells via a cholinergic pathway; released histamine from this source is largely responsbile for gastric ulceration through H1- and H2-receptor effects. Histamine H2-receptor-mediated gastric acid may play only a small contributory role in stress ulcers in rats. The antiulcer mechanisms of histamine H1- and H2-receptor blockade are discussed.
在应激性幽门结扎大鼠中研究了阿托品、甲氧苄胺嘧啶、甲硫米特或碳酸氢钠对胃溃疡形成、胃液分泌和胃肥大细胞脱颗粒的影响。还检测了地塞米松预处理对无幽门结扎动物(正常大鼠)应激性溃疡的影响。应激导致高发性腺病变和溃疡指数,并显著降低胃液分泌和腺壁肥大细胞计数。在应激前0.5小时注射,阿托品、甲氧苄胺嘧啶或甲硫米特强烈对抗溃疡形成。阿托品或甲硫米特可降低胃液分泌,但甲氧苄胺嘧啶无此作用。只有阿托品可防止应激诱导的肥大细胞变化。在应激前经胃内给予碳酸氢钠,尽管胃酸已完全中和,但并不能预防溃疡形成或肥大细胞脱颗粒。地塞米松诱导的胃黏膜肥大细胞减少可减轻应激性溃疡。研究结果表明,应激通过胆碱能途径使胃肥大细胞脱颗粒;由此释放的组胺主要通过H1和H2受体效应导致胃溃疡形成。组胺H2受体介导的胃酸在大鼠应激性溃疡中可能仅起小部分作用。讨论了组胺H1和H2受体阻断的抗溃疡机制。