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[小鼠心肌缺血诱导穴位敏化后背根神经节神经元TTX-R/TTX-S钠通道变化机制的研究]

[Study on mechanisms of changes of TTX-R/TTX-S sodium channels in dorsal root ganglion neurons after acupoint sensitization induced by myocardial ischemia in mice].

作者信息

DU Rui-Bing, He Hong-Zhou, Wu Yu-Wei, Xue Si-Meng, Diao Zhi-Jun, Gao Xin-Yan, Li Zhi-Gang, Qiao Hai-Fa

机构信息

College of Acupuncture-moxibustion and Massage, Shaanxi University of Chinese Medicine, Xianyang 712046, Shaanxi Province, China.

Shaanxi Key Laboratory of Acupuncture-Medicine Combination, Xianyang 712046, Shaanxi Province.

出版信息

Zhen Ci Yan Jiu. 2025 Jul 25;50(7):743-753. doi: 10.13702/j.1000-0607.20241077.

Abstract

OBJECTIVES

To explore the relation between acupoint sensitization and alterations of electrical signals of dorsal root ganglion (DRG) neurons from the perspective of ion channel dynamics in myocardial ischemia (MI) model mice.

METHODS

Sixty-four male C57BL/6J mice were randomly assigned to control and model groups (=32/group). The MI model was established by ligation of the left anterior descending (LAD) of the coronary artery. The MI was monitored by observing changes of ST segment of the standard limb-lead II of electrocardiogram (ECG-ST). 2, 3, 5-triphenyltetrazolium chloride (TTC) and H.E. staining were used to evaluate the infarct area and histopathological changes in the myocardial tissue. Evans blue (EB) staining was administered via tail vein injection to observe the location, distribution, and quantity of exudate points on the body surface in both groups. Nociceptive changes were evaluated by measuring mechanical pain and thermal pain thresholds. Subsequently, electrophysiological assessments were conducted to evaluate whole-cell membrane currents, intrinsic excitability, and Na channel current variations in different types of DRG neurons.

RESULTS

Compared with the control group, the ECG-ST segment in the model group was significantly elevated (<0.000 1), suggesting an induction of MI. TTC and H.E. staining showed a significant increase in the MI area (<0.001), accompanied by evident histopathological features such as myocardial fiber damage and inflammatory cell infiltration. The number of EB exudate points was significantly increased (<0.01), mainly distributing in the skin innervated by the T1-T5 spinal cord segments, as well as in the acupoints of "Feishu"(BL13), "Jueyinshu"(BL14) and"Xinshu"(BL15). Mechanical retraction reflex thresholds of the left upper and lower limbs of the model group significantly reduced (<0.000 1), and the thermal retraction latency of the left upper and lower limbs were notably shortened in the model group (<0.01, 0.000 1), and the mechanical pressure pain threshold on the left dorsal skin significantly reduced (<0.001). The DRG medium-sized neurons displayed an obvious decrease in rheobase (<0.05), along with a notable increase in whole-cell membrane current, spike number, and average instantaneous frequency (<0.05), reflecting enhanced intrinsic excitability. The activation curves of TTX-R/TTX-S sodium channels shifted towards hyperpolarization (<0.001), while the inactivation curves moved towards depolarization (<0.01).

CONCLUSIONS

DRG medium-sized neurons in the T1-T5 spinal cord segments may influence the acupoint sensitization of the body surface by modifying their Na channel kinetic properties.

摘要

目的

从离子通道动力学角度探讨心肌缺血(MI)模型小鼠背根神经节(DRG)神经元电信号变化与穴位敏化之间的关系。

方法

64只雄性C57BL/6J小鼠随机分为对照组和模型组(每组32只)。通过结扎冠状动脉左前降支建立MI模型。通过观察心电图标准肢体导联II的ST段变化(ECG-ST)监测MI情况。采用2,3,5-氯化三苯基四氮唑(TTC)和苏木精-伊红(H.E.)染色评估心肌组织梗死面积和组织病理学变化。通过尾静脉注射伊文思蓝(EB)染色观察两组体表渗出点的位置、分布和数量。通过测量机械性疼痛和热痛阈值评估伤害性感受变化。随后进行电生理评估,以评估不同类型DRG神经元的全细胞膜电流、内在兴奋性和钠通道电流变化。

结果

与对照组相比,模型组的ECG-ST段显著升高(<0.0001),提示MI诱导成功。TTC和H.E.染色显示MI面积显著增加(<0.001),伴有心肌纤维损伤和炎性细胞浸润等明显的组织病理学特征。EB渗出点数量显著增加(<0.01),主要分布在T1-T5脊髓节段支配的皮肤以及“肺俞”(BL13)、“厥阴俞”(BL14)和“心俞”(BL15)穴位处。模型组左上肢和下肢的机械回缩反射阈值显著降低(<0.0001),模型组左上肢和下肢的热回缩潜伏期明显缩短(<0.01,0.0001),左背部皮肤的机械压痛阈值显著降低(<0.001)。DRG中型神经元的基强度明显降低(<0.05),同时全细胞膜电流、动作电位发放数量和平均瞬时频率显著增加(<0.05),反映内在兴奋性增强。TTX-R/TTX-S钠通道的激活曲线向超极化方向移动(<0.001),而失活曲线向去极化方向移动(<0.01)。

结论

T1-T5脊髓节段的DRG中型神经元可能通过改变其钠通道动力学特性影响体表穴位敏化。

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