DI Wen-Hui, Huang Ke-Ni, Yi Li-Chen, Long Hao-Xi, Liang Xuan-Hao, Gu Jun, Liu Lin, Xu En-Zhe, Xu Neng-Gui, Yao Lu-Lu
Clinical School of Acupuncture and Rehabilitation, Guangzhou University of Chinese Medicine, Guangzhou 510006, China.
South China Research Center for Acupuncture and Moxibustion, Guangzhou University of Chinese Medicine, Guangzhou 510006.
Zhen Ci Yan Jiu. 2025 Aug 25;50(8):862-871. doi: 10.13702/j.1000-0607.20250444.
To investigate the mechanisms by which the hypoglossal nucleus (12N) modulates swallowing-related activities and mediates the therapeutic effects of electroacupuncture (EA) at "Lianquan" (CV23) in alleviating post-stroke dysphagia (PSD).
Tracer viruses were used to investigate the brain regions that directly project to CV23. C57BL/6J mice were divided into 7 groups:control, model, model+EA, normal+12N inhibition control, normal+12N inhibition, model+EA+12N inhibition control, and model+EA+12N inhibition groups (7 mice/group). Three additional C57BL/6J mice were used for the virus tracing experiment. A photochemical thrombosis model was established in C57BL/6J mice to simulate PSD, by intraperitoneally injecting 0.2 mL of 1.5% rose bengal solution combined with laser irradiation to induce ischemic pathological changes in the primary motor cortex;EA at CV23 (2 Hz, 1 mA, for 15 minutes, once in total) to study the effect of electroacupuncture on swallowing function in PSD mice. Chemogenetic viral inhibition was applied to suppress neuronal activity in the 12N, and changes in vocal fold movements and swallowing electromyography were observed under physiological conditions, by laryngoscopy and electrophysiological recorder respectively. After PSD model establishment, EA combined with chemogenetic inhibition of 12N was followed to observe the effect of chemogenetic inhibition of 12N on EA at CV23 in improving PSD. Tracer viruses were used to trace the upper brain region of the 12N.
The 12N directly projected to the surrounding tissues of CV23. Compared with the control group, in the model group, food residues were observed in the pharyngeal cavity and piriform recesses, along with prolonged vocal cord movement cycle time, a reduced number of vocal cord movement cycles within 10 seconds (<0.01), and decreased electromyographic area under the curve as well as reduced number of swallows (<0.001, <0.01). Compared with the model group, the model+EA group showed shortened vocal cord movement cycle time, an increased number of vocal cord movement cycles within 10 seconds (<0.01), and an enlarged electromyographic area under the curve (<0.001). Physiologically, compared with the normal+12N inhibition control group, the normal+12N inhibition group showed a reduction in the area under the swallowing electromyography curve and a decrease in the number of swallows (<0.05). Pathologically, laryngoscopy showed that compared with the model+EA+12N inhibition control group, the vocal fold movement cycle time of the model+EA+12N inhibition group was prolonged, and the number of movement cycles within 10 seconds was reduced (<0.01), the area under the swallowing electromyography curve was decreased (<0.05). The upstream brain regions of the 12N projecting to the surrounding tissues of CV23 were mainly identified in the nucleus tractus solitarii (NTS), intermediate reticular nucleus (IRt), spinal trigeminal nucleus caudalis (SP5C) and lateral paragigantocellular nucleus (LPGi), etc.
The 12N directly projects to the surrounding tissues of CV23 and contributes to EA-mediated improvement in PSD.
探讨舌下神经核(12N)调节吞咽相关活动及介导电针“廉泉”(CV23)改善脑卒中后吞咽困难(PSD)治疗效果的机制。
采用示踪病毒研究直接投射至CV23的脑区。将C57BL/6J小鼠分为7组:对照组、模型组、模型+电针组、正常+12N抑制对照组、正常+12N抑制组、模型+电针+12N抑制对照组、模型+电针+12N抑制组(每组7只小鼠)。另取3只C57BL/6J小鼠用于病毒示踪实验。通过腹腔注射0.2 mL 1.5%孟加拉玫瑰红溶液并结合激光照射诱导初级运动皮层缺血性病理改变,建立C57BL/6J小鼠光化学血栓形成模型以模拟PSD;对CV23进行电针(2 Hz,1 mA,15分钟,共1次),研究电针对PSD小鼠吞咽功能的影响。应用化学遗传病毒抑制法抑制12N中的神经元活动,分别通过喉镜和电生理记录仪观察生理条件下声带运动和吞咽肌电图的变化。建立PSD模型后,采用电针联合12N化学遗传抑制,观察12N化学遗传抑制对CV23电针改善PSD的影响。采用示踪病毒追踪12N的上位脑区。
12N直接投射至CV23周围组织。与对照组相比,模型组可见咽腔和梨状隐窝有食物残留,声带运动周期时间延长,10秒内声带运动周期次数减少(<0.01),吞咽肌电图曲线下面积减小,吞咽次数减少(<0.001,<0.01)。与模型组相比,模型+电针组声带运动周期时间缩短,10秒内声带运动周期次数增加(<0.01),吞咽肌电图曲线下面积增大(<0.001)。生理状态下,与正常+12N抑制对照组相比,正常+12N抑制组吞咽肌电图曲线下面积减小,吞咽次数减少(<0.05)。病理状态下,喉镜检查显示,与模型+电针+12N抑制对照组相比,模型+电针+12N抑制组声带运动周期时间延长,10秒内运动周期次数减少(<0.01),吞咽肌电图曲线下面积减小(<0.05)。投射至CV23周围组织的12N上位脑区主要位于孤束核(NTS)、中间网状核(IRt)、三叉神经脊束核尾侧亚核(SP5C)和外侧旁巨细胞网状核(LPGi)等。
12N直接投射至CV23周围组织,有助于电针介导的PSD改善。