首页> 外文期刊>European Journal of Pharmacology: An International Journal >Omeprazole-induced slowing of gastrointestinal transit in mice can be countered with tegaserod.
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Omeprazole-induced slowing of gastrointestinal transit in mice can be countered with tegaserod.

机译:奥美拉唑诱导的小鼠胃肠运输减慢可以用替加色罗抵消。

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摘要

Omeprazole, besides suppressing gastric acid, causes delayed gastric emptying, which may be associated with aggravated dyspeptic symptoms. Effects of omeprazole on small intestinal transit are unknown. In this study, we evaluated in mice if (a) omeprazole affects transit of a meal through the stomach and small intestine and (b) co-treatment with the promotility agent, tegaserod, can prevent the slowing effect of omeprazole. Omeprazole (40-150 mg/kg, i.p. once daily for 5 days) delayed gastric emptying of the meal in a dose-related manner. Small intestinal transit was then evaluated at the lowest dose of omeprazole (40 mg/kg) that did not retard gastric emptying. Such transit was significantly delayed after this dose of omeprazole compared with vehicle-treated controls. When tegaserod (0.10 mg/kg) was administered concomitantly with the omeprazole, small intestinal transit of the meal was not slowed and was not different from controls. These results show that omeprazole reduces aboral transit of luminalcontents through the stomach and small bowel of mice and that this delay is reversed by tegaserod.
机译:奥美拉唑除了抑制胃酸外,还会导致胃排空延迟,这可能与消化不良症状加重有关。奥美拉唑对小肠运输的影响尚不清楚。在这项研究中,我们在小鼠中评估了(a)奥美拉唑是否影响膳食通过胃和小肠的运输,以及(b)与促进剂替加色罗共同治疗是否可以防止奥美拉唑的减慢作用。奥美拉唑(40-150 mg / kg,腹膜内注射,每天一次,持续5天)以剂量相关的方式延迟了餐点的胃排空。然后以不延迟胃排空的最低剂量奥美拉唑(40 mg / kg)评估小肠运输。与赋形剂处理的对照组相比,这种剂量的奥美拉唑给药后这种转运明显延迟。与奥美拉唑同时使用替加色罗(0.10 mg / kg)时,膳食的小肠转运不会减慢,与对照组无差异。这些结果表明,奥美拉唑减少了小鼠胃部和小肠的管腔内含物的空肠转运,而这种延迟被替加色罗逆转了。

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