Department of Neurology, Philipps-University Marburg, Marburg, Germany.
Mov Disord. 2013 Apr;28(4):529-33. doi: 10.1002/mds.25246. Epub 2012 Dec 12.
Pancreatic polypeptide is released immediately after food ingestion. The release is operated by vagal-abdominal projections and has therefore been suggested as a test for vagal nerve integrity. Pathoanatomical and clinical studies indicate vagal dysfunction in early Parkinson's disease (PD).
We assessed the postprandial secretion of pancreatic polypeptide and motilin in healthy controls (n = 18) and patients with idiopathic rapid-eye-movement sleep behavior disorder (iRBD, n = 10), a potential premotor stage of PD, as well as in drug-naive (n = 19) and treated (n = 19) PD patients.
The postprandial pancreatic polypeptide secretion showed a physiological pattern in all groups and even an enhanced response in drug-naive PD and iRBD. Motilin concentrations correlated with pancreatic polypeptide concentrations.
Postprandial pancreatic polypeptide secretion is not a suitable test for vagal nerve integrity in PD. The unimpaired pancreatic polypeptide response in iRBD and PD might be explained by partially intact vagal-abdominal projections or compensatory mechanisms substituting a defective neuronal brain-gut axis.
进食后会立即释放胰多肽。这种释放是通过迷走神经-腹部投射来操作的,因此被认为是检测迷走神经完整性的一种方法。病理解剖学和临床研究表明,在早期帕金森病(PD)中存在迷走神经功能障碍。
我们评估了健康对照组(n=18)、特发性快速眼动睡眠行为障碍(iRBD,n=10)患者(PD 的潜在前驱期)以及未经药物治疗的 PD 患者(n=19)和接受药物治疗的 PD 患者(n=19)餐后胰多肽和胃动素的分泌情况。
所有组的餐后胰多肽分泌均呈现出生理模式,甚至未经药物治疗的 PD 和 iRBD 患者的反应增强。胃动素浓度与胰多肽浓度相关。
餐后胰多肽分泌不能作为 PD 迷走神经完整性的合适检测方法。iRBD 和 PD 中未受损的胰多肽反应可能是由于部分完整的迷走神经-腹部投射或替代有缺陷的神经元-肠脑轴的代偿机制所致。