Kaneko H, Mitsuma T, Uchida K, Nagai H, Harada M, Kotera H
Fourth Department of Internal Medicine, Aichi Medical University, Japan.
Dig Dis Sci. 1995 Sep;40(9):2043-51. doi: 10.1007/BF02208677.
Nizatidine, a new histamine-2-receptor antagonist, stimulates gastrointestinal motility in dogs and gastric emptying of liquids in rats. Effect of nizatidine on gastric emptying of a solid meal was investigated using a novel gastric emptying model in rats. Male Wistar rats (weighing 200-300 g) were supplied with powdered food containing 30 w/w% barium 14 hr before the beginning of the experiment and x-ray photography of rat stomach was taken under light ether anesthesia. Gastric emptying was assessed by percentage of a decrease in area 30 min after drug was injected intraperitoneally. There was a positive correlation between the area of the gastric outline and the weight of the gastric contents (r = 0.94, P < 0.01). Ether anesthesia itself did not affect gastric emptying. Nizatidine increased gastric emptying dose-dependently (emptied percentage; vehicle: 4.9 +/- 1.5%, 1 mg/kg: 7.2 +/- 0.4%, 3 mg/kg: 10.4 +/- 2.0%, 10 mg/kg: 16.7 +/- 4.9%, 30 mg/kg: 25.7 +/- 7.4%). N-Desmethyl nizatidine (NDM) also stimulated gastric emptying, but nizatidine S-oxide, cimetidine, an famotidine had no significant effects on gastric emptying. Nizatidine and neostigmine, but not NDM, at a subthreshold dose accelerated gastric emptying treated with a low dose of acetylcholine (0.1 mg/kg). Atropine (2 mg/kg, -30 min) did not modulate the gastroprokinetic action of nizatidine, but blocked that of NDM. These findings suggest that this noninvasive method may allow measurement of gastric emptying of solids accurately and that nizatidine and NDM facilitate gastric emptying probably mediated by a direct and/or an indirect (acetylcholinesterase inhibition) cholinergic mechanism.
尼扎替丁是一种新型组胺-2受体拮抗剂,可刺激犬的胃肠蠕动并促进大鼠液体的胃排空。使用一种新型大鼠胃排空模型研究了尼扎替丁对固体食物胃排空的影响。在实验开始前14小时,给雄性Wistar大鼠(体重200-300克)提供含30%(w/w)硫酸钡的粉末状食物,并在轻度乙醚麻醉下对大鼠胃进行X射线摄影。通过腹腔注射药物30分钟后胃轮廓面积减少的百分比来评估胃排空情况。胃轮廓面积与胃内容物重量之间存在正相关(r = 0.94,P < 0.01)。乙醚麻醉本身不影响胃排空。尼扎替丁剂量依赖性地增加胃排空(排空百分比;溶媒:4.9±1.5%,1毫克/千克:7.2±0.4%,3毫克/千克:10.4±2.0%,10毫克/千克:16.7±4.9%,30毫克/千克:25.7±7.4%)。N-去甲基尼扎替丁(NDM)也刺激胃排空,但尼扎替丁S-氧化物、西咪替丁和法莫替丁对胃排空无显著影响。尼扎替丁和新斯的明在阈下剂量时可加速低剂量乙酰胆碱(0.1毫克/千克)处理后的胃排空,但NDM无此作用。阿托品(2毫克/千克,-30分钟)不调节尼扎替丁的促胃动力作用,但可阻断NDM的促胃动力作用。这些发现表明,这种非侵入性方法可能允许准确测量固体食物的胃排空,并且尼扎替丁和NDM促进胃排空可能是由直接和/或间接(乙酰胆碱酯酶抑制)胆碱能机制介导的。