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口服纳洛酮可拮抗洛哌丁胺引起的口盲肠转运延迟。

Oral naloxone antagonizes loperamide-induced delay of orocecal transit.

作者信息

Basilisco G, Camboni G, Bozzani A, Paravicini M, Bianchi P A

出版信息

Dig Dis Sci. 1987 Aug;32(8):829-32. doi: 10.1007/BF01296704.

Abstract

Orocecal transit time was determined by the lactulose hydrogen breath test in nine healthy volunteers after administration of placebo, loperamide (16 mg per os), and loperamide (16 mg per os) followed by oral naloxone at doses of 16 and 32 mg. The four tests were performed in double-blind conditions and in random sequences. Transit time (mean, SD) after loperamide (128.8 min, 32.9) was significantly increased (P less than 0.05) compared with placebo (85.5 min, 35.7), loperamide followed by naloxone 16 mg (88.8 min, 46.2), and loperamide followed by naloxone 32 mg (84.4 min, 40.6). These results show that the peripheral opioid agonist loperamide delays orocecal transit in healthy subjects and that naloxone per os at adequate doses antagonizes this effect.

摘要

在9名健康志愿者中,通过乳果糖氢呼气试验测定了口服安慰剂、洛哌丁胺(16毫克口服)以及洛哌丁胺(16毫克口服)后再分别口服16毫克和32毫克纳洛酮后的口盲肠转运时间。这四项试验在双盲条件下随机顺序进行。与安慰剂(85.5分钟,标准差35.7)、洛哌丁胺后口服16毫克纳洛酮(88.8分钟,标准差46.2)以及洛哌丁胺后口服32毫克纳洛酮(84.4分钟,标准差40.6)相比,洛哌丁胺(128.8分钟,标准差32.9)后的转运时间显著延长(P小于0.05)。这些结果表明,外周阿片类激动剂洛哌丁胺会延迟健康受试者的口盲肠转运,且口服适当剂量的纳洛酮可拮抗这一效应。

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