Curcic J, Schwizer A, Kaufman E, Forras-Kaufman Z, Banerjee S, Roy S, Pal A, Hebbard G S, Boesiger P, Fried M, Steingoetter A, Schwizer W, Fox M
Institute for Biomedical Engineering, University and ETH Zurich, Zurich, Switzerland; Division of Gastroenterology and Hepatology, University Hospital Zurich, Zurich, Switzerland.
Aliment Pharmacol Ther. 2014 Nov;40(10):1230-40. doi: 10.1111/apt.12956. Epub 2014 Sep 17.
The mechanism of reflux protection may involve a 'flap valve' at the oesophago-gastric junction (OGJ).
To assess the effects of baclofen, a gamma-aminobutyric acid receptor type-B (GABA-B) agonist known to suppress reflux events, on the 'functional anatomy' of the OGJ and proximal stomach after a large test meal.
Twelve healthy volunteers (HVs) and 12 patients with gastro-oesophageal reflux disease (GERD); with erosive oesophagitis or pathological oesophageal acid exposure completed a randomised, double-blind, cross-over study. On 2 test days participants received 40-mg baclofen or placebo before ingestion of a large test meal. OGJ structure and function were assessed by high-resolution manometry (HRM) and magnetic resonance imaging (MRI) using validated methods. Measurements of the oesophago-gastric angle were derived from three-dimensional models reconstructed from anatomic MRI images. Cine-MRI and HRM identified postprandial reflux events. Mixed model analysis and Wilcoxon rank signed tests assessed differences between participant groups and treatment conditions.
In both HVs and GERD patients, baclofen reduced the frequency of postprandial reflux events. The oesophago-gastric insertion angle in GERD patients was reduced (-4.1 ± 1.8, P = 0.025), but was unchanged in healthy controls. In both study groups, baclofen augmented lower oesophageal sphincter (LES) pressure (HVs: +7.3 ± 1.8 mmHg, P < 0.0001, GERD: +4.50 ± 1.49 mmHg, P < 0.003) and increased LES length (HVs: +0.48 ± 0.11 cm, P < 0.0003, GERD: +0.35 ± 0.06 cm, P < 0.0001).
Baclofen inhibits transient LES relaxations and augments LES pressure and length. Additionally, baclofen has effects on the 'functional anatomy' of the OGJ and proximal stomach in GERD patients, which may suppress reflux by means of a 'flap valve' mechanism.
反流保护机制可能涉及食管胃交界处(OGJ)的“瓣阀”。
评估巴氯芬(一种已知可抑制反流事件的γ-氨基丁酸B型(GABA-B)受体激动剂)对大量试验餐后OGJ和胃近端“功能解剖结构”的影响。
12名健康志愿者(HV)和12名胃食管反流病(GERD)患者;患有糜烂性食管炎或病理性食管酸暴露的患者完成了一项随机、双盲、交叉研究。在2个试验日,参与者在摄入大量试验餐之前接受40毫克巴氯芬或安慰剂。使用经过验证的方法,通过高分辨率测压法(HRM)和磁共振成像(MRI)评估OGJ的结构和功能。食管胃角的测量值来自从解剖MRI图像重建的三维模型。电影MRI和HRM确定餐后反流事件。混合模型分析和Wilcoxon秩和检验评估参与者组和治疗条件之间的差异。
在HV和GERD患者中,巴氯芬均降低了餐后反流事件的频率。GERD患者的食管胃插入角减小(-4.1±1.8,P = 0.025),但在健康对照中未发生变化。在两个研究组中,巴氯芬均增加了食管下括约肌(LES)压力(HV:+7.3±1.8 mmHg,P < 0.0001,GERD:+4.50±1.49 mmHg,P < 0.003)并增加了LES长度(HV:+0.48±0.11 cm,P < 0.0003,GERD:+0.35±0.06 cm,P < 0.0001)。
巴氯芬抑制LES的短暂松弛并增加LES压力和长度。此外,巴氯芬对GERD患者的OGJ和胃近端“功能解剖结构”有影响,这可能通过 “瓣阀” 机制抑制反流。