利用 Fos-CreER 策略,绘制不同频率的电针 ST36 对不同脑区的激活图

Zi Guo, Naixuan Wei, Ru Ye, Tiancheng Sun, Shuang Qiu, Xiaomei Shao, Xiaochang Ge, Lu Guan, Junfang Fang, Jianqiao Fang, Junying Du
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引用次数: 0

摘要

电针(EA)是治疗疼痛的一种替代疗法。不同频率的电针具有不同的止痛效果,但其中心机制仍不甚明了。 FosTRAP:Ai9 小鼠被分为三组(假、2 Hz 和 100 Hz)。小鼠在祖山里(ST36)EA 30 分钟后立即腹腔注射 4-羟基他莫昔芬(4-OHT),记录激活的神经元。一周后,小鼠被处死,测定丘脑、杏仁核、皮层和下丘脑中被EA激活的TRAP处理神经元数量。 在大脑皮层,在扣带回皮层 1 区(Cg1)和初级躯体感觉皮层(S1),2 赫兹 EA 比 100 赫兹 EA 激活的 TRAP 处理神经元更多,2 赫兹和 100 赫兹 EA 与假 EA 没有区别。在岛叶皮层(IC)和次级躯体感觉皮层(S2),2赫兹EA激活的TRAP处理神经元与100赫兹和假EA激活的神经元相比上调。在丘脑中,与假 EA 激活的神经元相比,2 Hz EA 激活的丘脑室旁核(PV)中 TRAP 处理的神经元数量增加。在丘脑腹外侧核(VL),与 100 Hz EA 相比,2 Hz EA 激活的 TRAP 处理神经元数量显著增加,而假 EA 与 2 Hz EA 或 100 Hz EA 相比没有差异。与 100 Hz 或假 EA 相比,2 Hz EA 更频繁地激活丘脑腹后外侧核(VPL)中的 TRAP 处理神经元。 低频 EA ST36 能有效激活 Cg1、S1、S2、IC、VPL、PV 和 VL 中的神经元。低频 EA 所诱导的上述神经核的兴奋性增强可能与其在治疗神经病理性疼痛方面的卓越疗效有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Map activation of various brain regions using different frequencies of electroacupuncture ST36, utilizing the Fos-CreER strategy
Electroacupuncture (EA) is an alternative treatment option for pain. Different frequencies of EA have different pain-relieving effects; however, the central mechanism is still not well understood. The FosTRAP:Ai9 mice were divided into three groups (sham, 2 Hz, and 100 Hz). The mice were intraperitoneally injected with 4-hydroxytamoxifen (4-OHT) immediately after EA at Zusanli (ST36) for 30 min to record the activated neurons. One week later, the mice were sacrificed, and the number of TRAP-treated neurons activated by EA in the thalamus, amygdala, cortex, and hypothalamus was determined. In the cortex, 2 Hz EA activated more TRAP-treated neurons than 100 Hz EA did in the cingulate cortex area 1 (Cg1) and primary somatosensory cortex (S1), and 2 Hz and 100 Hz EAs did not differ from sham EA. TRAP-treated neurons activated by 2 Hz EA were upregulated in the insular cortex (IC) and secondary somatosensory cortex (S2) compared with those activated by 100 Hz and sham EA. In the thalamus, the number of TRAP-treated neurons activated by 2 Hz EA was elevated in the paraventricular thalamic nucleus (PV) compared with those activated by sham EA. In the ventrolateral thalamic nucleus (VL), the number of TRAP-treated neurons activated by 2 Hz EA was significantly upregulated compared with those activated by 100 Hz EA, and sham EA showed no difference compared to 2 Hz EA or 100 Hz EA. TRAP-treated neurons were more frequently activated in the ventral posterolateral thalamic nucleus (VPL) by 2 Hz EA than by 100 Hz or sham EA. Low-frequency EA ST36 effectively activates neurons in the Cg1, S1, S2, IC, VPL, PV, and VL. The enhanced excitability of the aforementioned nuclei induced by low-frequency EA may be related to its superior efficacy in the treatment of neuropathological pain.
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