Wingate Institute, Centre for Digestive Diseases, Barts and the London School of Medicine and Dentistry, Queen Mary University of London, UK.
Aliment Pharmacol Ther. 2012 Feb;35(3):319-26. doi: 10.1111/j.1365-2036.2011.04955.x. Epub 2011 Dec 27.
BACKGROUND: Acid infusion in humans induces primary and secondary oesophageal hypersensitivity. The effects of pregabalin, a centrally-acting modulator of voltage-sensitive calcium channels, on development of acid-induced oesophageal hypersensitivity remain unknown. AIM: To study the effects of pregabalin on development of secondary oesophageal hypersensitivity in healthy humans. METHODS: Placebo-controlled, double-blind, randomised, cross-over study of 15 healthy volunteers (six women, age 21-56 years). After oesophageal manometry, baseline pain thresholds (PTs) to proximal oesophageal electrical stimulation were determined using bipolar ring electrodes. A 30-min infusion of HCl was performed in the distal oesophagus followed by PT measurements at 30 and 90 min. This protocol was repeated after administration of pregabalin (dosing schedule: 75 mg twice daily for 3 days then 150 mg twice daily for 1 day and then 150 mg on the morning of study) or placebo. RESULTS: T0 PTs were similar in patients after receiving placebo or pregabalin [mean (s.d.) 32.9 mA (20.5) vs. 34.1 (15.7), P = 0.42]. Pregabalin reduced development of acid-induced hypersensitivity in the proximal oesophagus at 30 min [mean change in PT (C.I.) placebo -6.2 mA (-11.3 to +1.3) vs. pregabalin +0.20 mA (-2.7 to +3.3)] and 90 min [placebo -3.7 mA (-10.0 to +2.0) vs. pregabalin +0.7 mA (-4.7 to 7.3)] overall P = 0.001. Pregabalin reduced median visual analogue scale score for acid-induced pain (1/10 vs. placebo 3/10, P = 0.027). CONCLUSIONS: Pregabalin attenuates development of secondary hypersensitivity in the proximal oesophagus after distal oesophageal acidification; it may thus have a role in treatment of patients with proven oesophageal pain hypersensitivity.
背景:在人体中进行酸灌注会引起原发性和继发性食管高敏性。电压敏感性钙通道的中枢作用调节剂普瑞巴林对酸诱导的食管高敏性发展的影响尚不清楚。
目的:研究普瑞巴林对健康人群中继发性食管高敏性发展的影响。
方法:这是一项安慰剂对照、双盲、随机、交叉研究,纳入了 15 名健康志愿者(6 名女性,年龄 21-56 岁)。食管测压后,使用双极环电极确定近端食管电刺激的基础疼痛阈值(PTs)。在远端食管进行 30 分钟的 HCl 灌注,然后在 30 分钟和 90 分钟测量 PT。在给予普瑞巴林(剂量方案:75mg 每日两次,持续 3 天,然后 150mg 每日两次,持续 1 天,然后在研究当天早上给予 150mg)或安慰剂后重复该方案。
结果:接受安慰剂或普瑞巴林后,T0 时的 PTs 在患者中相似[平均(标准差)32.9mA(20.5)与 34.1(15.7),P=0.42]。普瑞巴林在 30 分钟时降低了近端食管酸诱导的高敏性发展[PT 变化的平均差值(CI)安慰剂-6.2mA(-11.3 至 +1.3)与普瑞巴林+0.20mA(-2.7 至 +3.3)]和 90 分钟时[安慰剂-3.7mA(-10.0 至 +2.0)与普瑞巴林+0.7mA(-4.7 至 7.3)]总体 P=0.001。普瑞巴林降低了酸诱导疼痛的中位数视觉模拟量表评分(1/10 与安慰剂 3/10,P=0.027)。
结论:普瑞巴林可减轻远端食管酸化后近端食管的继发性高敏性发展;因此,它可能在治疗已证实的食管疼痛高敏性患者方面具有作用。
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