首页> 美国卫生研究院文献>Gut >Effects of single daily doses of a pyridil-2-tetrahydrothiophene derivative (40749 RP) on 24 hour H+ activity nocturnal acid output gastrin and pepsinogen I profiles in duodenal ulcer patients.
【2h】

Effects of single daily doses of a pyridil-2-tetrahydrothiophene derivative (40749 RP) on 24 hour H+ activity nocturnal acid output gastrin and pepsinogen I profiles in duodenal ulcer patients.

机译:每日一次剂量的吡啶-2--2-氢噻吩衍生物(40749 RP)对十二指肠溃疡患者24小时H +活性夜酸输出胃泌素和胃蛋白酶原I的影响。

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

40749 RP is a pyridil-2-tetrahydrothiophene derivative, belonging to a new class of gastric antisecretory drugs. We compared its effects on gastric secretion with cimetidine. Intragastric acidity, nocturnal acid output, gastrin and pepsinogen-I profiles were measured in patients with duodenal ulcer in clinical remission. A single dose of 100 mg 40749 RP reduced median 24 h gastric acidity as effectively as cimetidine 1000 mg given as four divided doses, 0.63 vs 1.6 mmol/l. Continued treatment with 40749 RP for 10 days reduced the median 24 h gastric acidity even further, to 0.006 mmol/l (p less than 0.001) and significantly increased fasting concentrations of gastrin and pepsinogen-I (p = 0.02). The incremental gastrin secretion to a standard meal was significantly increased after 10 days treatment with 40749 RP when compared with the first day of 40749 RP, or with cimetidine. These results show that 40749 RP exerts a powerful inhibitory effect on gastric acid secretion after a single 100 mg dose, and that this inhibitory effect increases with continued administration.
机译:40749 RP是吡啶-2--2-氢噻吩衍生物,属于一类新型的胃分泌药物。我们比较了西咪替丁对胃分泌的影响。在临床缓解期间,对十二指肠溃疡患者的胃内酸度,夜酸输出,胃泌素和胃蛋白酶原-I进行了测量。 100毫克40749 RP的单次剂量降低了24小时的胃酸中位数,与西咪替丁1000毫克(四次分剂量,分别为0.63对1.6 mmol / l)给予的降低一样。用40749 RP连续治疗10天甚至进一步降低了24 h胃酸中位值至0.006 mmol / l(p小于0.001),并显着增加了胃泌素和胃蛋白酶原I的空腹浓度(p = 0.02)。与40749 RP的第一天或西咪替丁相比,用40749 RP治疗10天后,标准餐的胃泌素分泌增加显着增加。这些结果表明40749 RP在单次100mg剂量后对胃酸分泌具有强大的抑制作用,并且该抑制作用随着连续给药而增加。

著录项

相似文献

  • 外文文献
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号