Cucchiara S, Minella R, Scoppa A, Emiliano M, Calabrese F, Az-Zeqeh N, Rea B, Salvia G
Department of Pediatrics, School of Medicine, University of Naples Federico II, Italy.
J Pediatr Gastroenterol Nutr. 1997 Apr;24(4):411-8. doi: 10.1097/00005176-199704000-00010.
The macrolide antibiotic erythromycin (EM) affects gastrointestinal motor activity by acting as agonist of motilin receptors located on the smooth muscle cells of the gastroduodenal tract. We studied the effect of intravenous EM on fasting antroduodenal motility in controls and children with gastrointestinal dysmotility.
EM lactobionate (rate, 3.0 mg/kg/h) was infused intravenously while antroduodenal manometry was recorded in 10 controls, in 7 patients with functional dyspepsia and in 6 patients with gut pseudo-obstruction. The mean (SD) age (years) was 5.7 (1.4), 6.5 (2.4), and 6.7 (3.2), respectively. Manometry was performed by means of a four- or six-lumen catheter introduced through the nose and perfused with a low compliance pneumohydraulic system. Five controls received EM and five received saline.
EM, infused 5 minutes after passage of an activity front (AF), induced in controls a premature antroduodenal AF occurring 15.4 +/- 3.2 minutes after starting infusion; no motor changes were seen after saline; duration and propagation velocity of EM-induced AFs did not differ from spontaneous AFs. In patients with functional dyspepsia EM induced various patterns such as premature antroduodenal AFs, antral phase III-like pattern with short duodenal bursts or prolonged phasic antral waves and no duodenal activity. In patients with neurogenic pseudo-obstruction rare or absent antral activity with incoordinated or absent duodenal activity was induced; no contractions were elicited in two patients with myogenic pseudo-obstruction.
It is confirmed that EM, given at subtherapeutic doses, is a powerful prokinetic agent that can have clinical applications in patients with gastrointestinal dysmotility; however, the effect of the drug seems to be influenced by the nature of the underlying disorder.
大环内酯类抗生素红霉素(EM)通过作为位于胃十二指肠平滑肌细胞上的胃动素受体的激动剂来影响胃肠运动活性。我们研究了静脉注射EM对健康对照者和胃肠动力障碍患儿空腹时胃十二指肠动力的影响。
静脉输注乳糖酸红霉素(速率为3.0mg/kg/h),同时对10名健康对照者、7名功能性消化不良患者和6名肠道假性梗阻患者进行胃十二指肠测压。平均(标准差)年龄(岁)分别为5.7(1.4)、6.5(2.4)和6.7(3.2)。通过经鼻插入的四腔或六腔导管进行测压,并使用低顺应性气液压系统进行灌注。5名对照者接受EM,5名接受生理盐水。
在活动波峰(AF)通过后5分钟输注EM,在对照者中诱导出提前出现的胃十二指肠AF,在开始输注后15.4±3.2分钟出现;输注生理盐水后未见运动变化;EM诱导的AF的持续时间和传播速度与自发AF无差异。在功能性消化不良患者中,EM诱导出各种模式,如提前出现的胃十二指肠AF、具有短十二指肠爆发或延长的阶段性胃窦波且无十二指肠活动的胃窦III期样模式。在神经源性假性梗阻患者中,诱导出罕见或无胃窦活动且十二指肠活动不协调或无十二指肠活动的情况;两名肌源性假性梗阻患者未引出收缩。
已证实,以亚治疗剂量给予的EM是一种强效促动力剂,可在胃肠动力障碍患者中具有临床应用价值;然而,药物的效果似乎受潜在疾病性质的影响。