Acupuncture Relieves Motion Sickness via the Irβ-Erk1/2-Dependent Insulin Receptor Signalling Pathway

针灸科 医学 运动病 胰岛素受体 胰岛素 药理学 内科学 物理医学与康复 精神科 胰岛素抵抗 病理 替代医学
作者
Dawei Tian,Fengfeng Mo,Xingjian Cai,Zhiyuan Miao,Feng Xiao,Yi-Fang Chang,Lusha Wu,Yuxiao Tang,Xin Wang,Chen Ye,Xiaolu Qian,Wei Gu,Min Li
出处
期刊:Acupuncture in Medicine [SAGE Publishing]
卷期号:36 (3): 153-161 被引量:10
标识
DOI:10.1136/acupmed-2016-011202
摘要

Objective Acupuncture has been widely used for the treatment of motion sickness (MS), but the underlying mechanisms are unclear. The aim of this research was to study the mechanism of acupuncture in the treatment of MS. Methods To observe the effects of acupuncture in the treatment of MS, 80 rats were randomised into five groups that were subjected to acceleration and either remained untreated (CTRL), or received restraint (REST), scopolamine (SCOP) or acupuncture at SP4 (sham) or PC6+ST36 (verum) acupuncture points. To study the mechanism underlying the effects of acupuncture in the treatment of MS, 48 rats were randomised into three groups: acupuncture+extracellular regulated protein kinases (ERK) 1/2 inhibitor (ERKinh), acupuncture+insulin receptor (IR) antagonist (IRant), and acupuncture+vehicle (VEH). After acceleration, the MS index (MSI) and spontaneous activity (SA) of the rats were recorded. Serum stress hormones, Fos-positive cells, c-fos mRNA in the vestibular nucleus, and IRβ-, p-IRβ-, ERK1/2- and p-ERK1/2-positive cells in the dorsal motor nucleus of the vagus nerve (DMV) were detected. Results After acceleration, MS symptoms in the PC6+ST36 and SCOP groups were reduced compared with the CTRL, REST, and SP4 groups. The number of p-IRβ- and p-ERK1/2-positive cells and insulin levels were higher in the PC6+ST36 group than in the CTRL, REST, and SP4 groups. After ERK1/2 inhibitor and IR antagonist treatment, MS symptoms in the VEH group were lower than in the ERKinh and IRant groups. Conclusions Our study demonstrates that acupuncture significantly alleviates MS through the IRβ-ERK1/2-dependent insulin receptor signalling pathway in the DMV
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