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序贯使用红霉素和奥曲肽对十二指肠测压的影响。

Effect of sequential erythromycin and octreotide on antroduodenal manometry.

作者信息

Di Lorenzo C, Lucanto C, Flores A F, Idries S, Hyman P E

机构信息

Department of Pediatrics, Children's Hospital of Pittsburgh, Pennsylvania 15213, USA.

出版信息

J Pediatr Gastroenterol Nutr. 1999 Sep;29(3):293-6. doi: 10.1097/00005176-199909000-00010.

DOI:10.1097/00005176-199909000-00010
PMID:10467994
Abstract

BACKGROUND

In earlier studies, erythromycin stimulated but octreotide inhibited gastric antral contractions, as each drug induced phase 3-like episodes.

METHODS

To assess the effect of erythromycin pretreatment on octreotide-induced changes in antroduodenal motility, 16 patients were studied (mean age, 8.7 +/- 1.5 years, 8 male): 6 with severe gastroesophageal reflux, 4 with cyclic vomiting, 3 with gastroparesis, 2 with chronic intestinal pseudo-obstruction, and 1 with Crohn's disease and unexplained nausea and vomiting. After recording fasting antroduodenal motility for 3 hours, 1 mg/kg intravenous erythromycin was administered over 30 minutes. Sixty minutes after the erythromycin infusion, 0.5 microg/kg subcutaneous octreotide was administered, followed 1 hour later by a meal.

RESULTS

Phase 3 occurred spontaneously in 10 patients and after erythromycin in 12 patients. When administered after erythromycin, octreotide immediately induced phase 3s contractions in 15 patients, beginning in the antrum. In 7 children, some of the octreotide-induced phase 3s did not propagate. After the meal, antral contractions continued in all patients. The fed pattern was replaced in 14 patients by alternating phase 3 and phase 1 activities.

CONCLUSIONS

Pretreatment with erythromycin prevented octreotide-induced inhibition of antral contractions. Inhibition of antral contractions by octreotide may be mediated through either a direct or indirect suppression of motilin release, because antral contractions persist after pretreatment with the motilin receptor agonist erythromycin.

摘要

背景

在早期研究中,红霉素可刺激胃窦收缩,而奥曲肽则抑制胃窦收缩,因为每种药物均可诱发类似Ⅲ期的收缩活动。

方法

为评估红霉素预处理对奥曲肽诱导的十二指肠运动变化的影响,对16例患者(平均年龄8.7±1.5岁,8例男性)进行了研究:6例患有严重胃食管反流,4例患有周期性呕吐,3例患有胃轻瘫,2例患有慢性假性肠梗阻,1例患有克罗恩病并伴有不明原因的恶心和呕吐。在记录3小时空腹十二指肠运动情况后,于30分钟内静脉注射1mg/kg红霉素。红霉素输注60分钟后,皮下注射0.5μg/kg奥曲肽,1小时后进食。

结果

10例患者自发出现Ⅲ期收缩,12例患者在使用红霉素后出现Ⅲ期收缩。在红霉素之后给予奥曲肽时,15例患者立即在胃窦开始出现Ⅲ期收缩。在7名儿童中,一些奥曲肽诱导的Ⅲ期收缩未传播。进食后,所有患者的胃窦收缩仍在继续。14例患者的进食模式被Ⅲ期和Ⅰ期活动交替所取代。

结论

红霉素预处理可预防奥曲肽诱导的胃窦收缩抑制。奥曲肽对胃窦收缩的抑制可能是通过直接或间接抑制胃动素释放介导的,因为在用胃动素受体激动剂红霉素预处理后胃窦收缩仍然持续。

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