Key Laboratory of Acupuncture and Neurology of Zhejiang Province, The Third Clinical Medical College, Zhejiang Chinese Medical University, Hangzhou, China.
NHC and CAMS Key Laboratory of Medical Neurobiology, MOE Frontier Science Center for Brain Research and Brain-Machine Integration, School of Brain Science and Brain Medicine, Zhejiang University, Hangzhou, China.
CNS Neurosci Ther. 2023 Dec;29(12):4043-4058. doi: 10.1111/cns.14328. Epub 2023 Jul 3.
Epidemiological studies in patients with neuropathic pain have demonstrated a strong association between neuropathic pain and psychiatric conditions such as anxiety. Preclinical and clinical work has demonstrated that electroacupuncture (EA) effectively alleviates anxiety-like behaviors induced by chronic neuropathic pain. In this study, a potential neural circuitry underlying the therapeutic action of EA was investigated.
The effects of EA stimulation on mechanical allodynia and anxiety-like behaviors in animal models of spared nerve injury (SNI) were examined. EA plus chemogenetic manipulation of glutamatergic (Glu) neurons projecting from the rostral anterior cingulate cortex (rACC ) to the dorsal raphe nucleus (DRN) was used to explore the changes of mechanical allodynia and anxiety-like behaviors in SNI mice.
Electroacupuncture significantly alleviated both mechanical allodynia and anxiety-like behaviors with increased activities of glutamatergic neurons in the rACC and serotoninergic neurons in the DRN. Chemogenetic activation of the rACC -DRN projections attenuated both mechanical allodynia and anxiety-like behaviors in mice at day 14 after SNI. Chemogenetic inhibition of the rACC -DRN pathway did not induce mechanical allodynia and anxiety-like behaviors under physiological conditions, but inhibiting this pathway produced anxiety-like behaviors in mice at day 7 after SNI; this effect was reversed by EA. EA plus activation of the rACC -DRN circuit did not produce a synergistic effect on mechanical allodynia and anxiety-like behaviors. The analgesic and anxiolytic effects of EA could be blocked by inhibiting the rACC -DRN pathway.
The role of rACC -DRN circuit may be different during the progression of chronic neuropathic pain and these changes may be related to the serotoninergic neurons in the DRN. These findings describe a novel rACC -DRN pathway through which EA exerts analgesic and anxiolytic effects in SNI mice exhibiting anxiety-like behaviors.
在患有神经性疼痛的患者中进行的流行病学研究表明,神经性疼痛与焦虑等精神疾病之间存在很强的关联。临床前和临床工作已经证明,电针(EA)有效地缓解了慢性神经性疼痛引起的焦虑样行为。在这项研究中,研究了 EA 治疗作用的潜在神经回路。
检查了 EA 刺激对 spared nerve injury (SNI) 动物模型中机械性痛觉过敏和焦虑样行为的影响。使用 EA 加谷氨酸能神经元(Glu)的化学遗传操作,来研究 SNI 小鼠的机械性痛觉过敏和焦虑样行为的变化。Glu 神经元从前扣带回皮质(rACC)投射到中缝背核(DRN)。
电针显著缓解了机械性痛觉过敏和焦虑样行为,同时增加了 rACC 中的谷氨酸能神经元和 DRN 中的 5-羟色胺能神经元的活性。rACC-DRN 投射的化学遗传激活减轻了 SNI 后第 14 天小鼠的机械性痛觉过敏和焦虑样行为。rACC-DRN 通路的化学遗传抑制在生理条件下不会引起机械性痛觉过敏和焦虑样行为,但在 SNI 后第 7 天会引起小鼠的焦虑样行为;这种效应被 EA 逆转。EA 加 rACC-DRN 回路的激活对机械性痛觉过敏和焦虑样行为没有协同作用。rACC-DRN 通路的抑制可以阻断 EA 的镇痛和抗焦虑作用。
rACC-DRN 回路在慢性神经性疼痛的进展过程中的作用可能不同,这些变化可能与 DRN 中的 5-羟色胺能神经元有关。这些发现描述了一个新的 rACC-DRN 通路,通过该通路,EA 在 SNI 小鼠中发挥镇痛和抗焦虑作用,同时表现出焦虑样行为。