Tack J
Centre for Gastroenterological Research, University Hospital Gasthuisberg, Catholic University of Leuven.
Acta Gastroenterol Belg. 1995 Jan-Feb;58(1):21-30.
The upper gastrointestinal tract displays two different functional states: the interdigestive or fasting state, and the fed state. The fasting state is characterized by a cyclical motor pattern, the migrating motor complex (MMC). The control of the MMC is incompletely understood. Plasma levels of the hormone motilin fluctuate in synchrony with MMC, but it is still controversial whether a motilin peak triggers the MMC or whether the MMC causes motilin release. We used the motilin agonistic properties of erythromycin to resolve this issue in man. Administration of a low dose of erythromycin induced a MMC which started from the gastric antrum, unaccompanied by a motilin peak. This finding argues against a release of motilin secondary to the MMC and supports our hypothesis that in man motilin peaks trigger the MMC. We observed that higher doses of erythromycin no longer induced a MMC, but stimulated antral contractility. The enteric nervous system is involved in the control of both the fasting and fed state at each level of the gastrointestinal tract. We hypothesized that the target for motilin to trigger the MMC is the enteric nervous system in the gastric antrum. Yet, no physiological data on antral enteric neurons were available. We performed the first electrophysiological study of myenteric neurons of the gastric antrum, revealing unique electrical and synaptic properties in comparison to other regions of the gastrointestinal tract. We confirmed the role of the enteric nervous system of the gastric antrum in the control of the MMC by directly demonstrating the presence of motilin receptors on a subpopulation of neurons. We demonstrated that endogenous and exogenous substances that stimulate (cholecystokinin, cisapride, erythromycin) or inhibit (norepinephrine, 5-hydroxytryptamine) gastric emptying all act on antral enteric neurons. These observations strongly support the hypothesis that the enteric nervous system in the gastric antrum plays a key role in the coordination of antral peristalsis and the regulation of gastric emptying. Finally, we hypothesized that the actions of erythromycin on motilin receptors on enteric neurons and intestinal smooth muscle offer a potential for therapeutic applications in gastrointestinal motility disorders. We confirmed this by demonstrating gastrointestinal motility stimulating activity of erythromycin in patients with diabetic gastroparesis.
消化间期或禁食状态以及进食状态。禁食状态的特征是一种周期性运动模式,即移行性运动复合波(MMC)。对MMC的控制尚未完全了解。激素胃动素的血浆水平与MMC同步波动,但胃动素峰值是触发MMC还是MMC导致胃动素释放仍存在争议。我们利用红霉素的胃动素激动特性在人体中解决了这个问题。给予低剂量的红霉素可诱导出从胃窦开始的MMC,且无胃动素峰值伴随。这一发现反对MMC继发胃动素释放的观点,并支持我们的假设,即在人体中胃动素峰值触发MMC。我们观察到更高剂量的红霉素不再诱导MMC,而是刺激胃窦收缩性。肠神经系统参与胃肠道各水平消化间期和进食状态的控制。我们假设胃动素触发MMC的靶点是胃窦的肠神经系统。然而,尚无关于胃窦肠神经元的生理学数据。我们首次对胃窦肌间神经元进行了电生理研究,发现其与胃肠道其他区域相比具有独特的电和突触特性。我们通过直接证明神经元亚群上存在胃动素受体,证实了胃窦肠神经系统在控制MMC中的作用。我们证明,刺激(胆囊收缩素、西沙必利、红霉素)或抑制(去甲肾上腺素、5-羟色胺)胃排空的内源性和外源性物质均作用于胃窦肠神经元。这些观察结果有力地支持了以下假设:胃窦的肠神经系统在协调胃窦蠕动和调节胃排空方面起关键作用。最后,我们假设红霉素对肠神经元和肠平滑肌上胃动素受体的作用为胃肠道动力障碍的治疗应用提供了潜力。我们通过证明红霉素对糖尿病胃轻瘫患者的胃肠动力刺激活性证实了这一点。