Centre for Neuroscience, Surgery and Trauma, Blizard Institute, Wingate Institute of Neurogastroenterology, Barts and the London School of Medicine & Dentistry, Mary University of London, London, UK.
Mech-Sense, Department of Gastroenterology, Aalborg University Hospital, Aalborg, Denmark.
Aliment Pharmacol Ther. 2020 Sep;52(6):988-996. doi: 10.1111/apt.15869. Epub 2020 Aug 7.
BACKGROUND: The vagus nerve exerts an anti-nociceptive effect on the viscera. AIM: To investigate whether transcutaneous vagal nerve stimulation (t-VNS) prevents the development of and/or reverses established visceral hypersensitivity in a validated model of acid-induced oesophageal pain. METHODS: Before and after a 30-minute infusion of 0.15M hydrochloric acid into the distal oesophagus, pain thresholds to electrical stimulation were determined in the proximal non-acid exposed oesophagus. Validated sympathetic (cardiac sympathetic index) and parasympathetic (cardiac vagal tone [CVT]) nervous system measures were recorded. In study 1, 15 healthy participants were randomised in a blinded crossover design to receive either t-VNS or sham for 30 minutes during acid infusion. In study 2, 18 different healthy participants were randomised in a blinded crossover design to receive either t-VNS or sham, for 30 minutes after acid infusion. RESULTS: Study 1: t-VNS increased CVT (31.6% ± 58.7 vs -9.6 ± 20.6, P = 0.02) in comparison to sham with no effect on cardiac sympathetic index. The development of acid-induced oesophageal hypersensitivity was prevented with t-VNS in comparison to sham (15.5 mA per unit time (95% CI 4.9 - 26.2), P = 0.004). Study 2: t-VNS increased CVT (26.3% ± 32.7 vs 3 ± 27.1, P = 0.03) in comparison to sham with no effect on cardiac sympathetic index. t-VNS reversed established acid-induced oesophageal hypersensitivity in comparison to sham (17.3mA/unit time (95% CI 9.8-24.7), P = 0.0001). CONCLUSIONS: t-VNS prevents the development of, and reverses established, acid-induced oesophageal hypersensitivity. These results have therapeutic implications for the management of visceral pain hypersensitivity.
背景:迷走神经对内脏发挥抗伤害作用。
目的:在酸诱导的食管疼痛的验证模型中,研究经皮迷走神经刺激(t-VNS)是否预防和/或逆转已建立的内脏高敏感性。
方法:在将 0.15M 盐酸输注到食管远端 30 分钟之前和之后,确定近端非酸暴露食管中电刺激的疼痛阈值。记录已验证的交感神经(心脏交感神经指数)和副交感神经(心脏迷走神经张力[CVT])神经测量值。在研究 1 中,15 名健康参与者以盲法交叉设计随机分为 t-VNS 或假刺激组,在酸输注期间接受 30 分钟的 t-VNS 或假刺激。在研究 2 中,18 名不同的健康参与者以盲法交叉设计随机分为 t-VNS 或假刺激组,在酸输注后接受 30 分钟的 t-VNS 或假刺激。
结果:研究 1:与假刺激相比,t-VNS 增加了 CVT(31.6%±58.7 比-9.6±20.6,P=0.02),而对心脏交感神经指数没有影响。与假刺激相比,t-VNS 预防了酸诱导的食管高敏感性的发展(单位时间 15.5 mA(95%CI 4.9-26.2),P=0.004)。研究 2:与假刺激相比,t-VNS 增加了 CVT(26.3%±32.7 比 3±27.1,P=0.03),而对心脏交感神经指数没有影响。与假刺激相比,t-VNS 逆转了已建立的酸诱导的食管高敏感性(单位时间 17.3 mA(95%CI 9.8-24.7),P=0.0001)。
结论:t-VNS 预防酸诱导的食管高敏感性的发展和逆转。这些结果对内脏疼痛高敏感性的管理具有治疗意义。
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