Zerbib F, Bruley Des Varannes S, Scarpignato C, Leray V, D'Amato M, Rozé C, Galmiche J P
Human Nutrition Research Center and Department of Gastroenterology and Hepatology, University of Nantes, 44035 Nantes, France.
Am J Physiol. 1998 Dec;275(6):G1266-73. doi: 10.1152/ajpgi.1998.275.6.G1266.
Transient lower esophageal sphincter (LES) relaxations (TLESRs) are the main underlying mechanism of gastroesophageal reflux. Although CCK acts through CCK-A receptors to increase the TLESRs induced by gastric distension, the respective roles of endogenous CCK and fundic tone in triggering postprandial TLESRs remain unknown. The aim of this study was to determine the effect of the CCK-A receptor antagonist, loxiglumide, on postprandial LES function and fundic tone in humans. LES motor events and fundic tone were simultaneously monitored in two groups of healthy volunteers. Recordings were performed during fasting and for 3 h after a liquid meal (200 ml/200 kcal) administered either orally or intraduodenally at a rate mimicking gastric emptying. Each subject received loxiglumide (10 mg. kg-1. h-1) or saline (control) in randomized order, which was started 40 min before the meal and maintained for 3 h thereafter. After the oral meal, loxiglumide significantly reduced TLESRs (P = 0.002) without significantly affecting LES pressure and fundic tone. After duodenal infusion of the meal, loxiglumide totally abolished the increase in TLESRs, reduced LES pressure fall (P < 0.02), and strongly inhibited fundic relaxation (P = 0.0001). We concluded that endogenous CCK is involved in the postprandial control of both LES function and fundic tone through activation of CCK-A receptors.
短暂性下食管括约肌(LES)松弛(TLESRs)是胃食管反流的主要潜在机制。尽管胆囊收缩素(CCK)通过CCK-A受体发挥作用,增加胃扩张诱导的TLESRs,但内源性CCK和胃底张力在引发餐后TLESRs中的各自作用仍不清楚。本研究的目的是确定CCK-A受体拮抗剂洛西肽胺对人体餐后LES功能和胃底张力的影响。在两组健康志愿者中同时监测LES运动事件和胃底张力。在禁食期间以及以模拟胃排空的速率口服或十二指肠内给予液体餐(200 ml/200 kcal)后持续3小时进行记录。每位受试者以随机顺序接受洛西肽胺(10 mg·kg-1·h-1)或生理盐水(对照),在进餐前40分钟开始给药,并在之后持续3小时。口服餐后,洛西肽胺显著降低TLESRs(P = 0.002),而对LES压力和胃底张力无显著影响。十二指肠内输注餐后,洛西肽胺完全消除了TLESRs的增加,降低了LES压力下降(P < 0.02),并强烈抑制胃底松弛(P = 0.0001)。我们得出结论,内源性CCK通过激活CCK-A受体参与餐后LES功能和胃底张力的控制。