中国临床解剖学杂志 ›› 2023, Vol. 41 ›› Issue (5): 557-564.doi: 10.13418/j.issn.1001-165x.2023.5.10

• 实验研究 • 上一篇    下一篇

腹内侧前额叶皮质锥体神经元参与选择性坐骨神经损伤小鼠疼痛和焦虑样行为调控的研究

林培敏1,     刘燕1,    刘婷2,    尹颢霖2,    张英1*   

  1. 1.西南医科大学附属中医医院麻醉科;    2.西南医科大学,  四川   泸州    646000
  • 收稿日期:2022-03-11 出版日期:2023-09-25 发布日期:2023-10-16
  • 通讯作者: 张英,教授,硕士研究生导师,E-mail:1125266775@qq.com
  • 作者简介:林培敏(1984-),女,硕士,主治医师,研究方向:神经病理性疼痛,E-mail:linpeimin001@163.com
  • 基金资助:
    四川省科技计划项目-应用基础研究(2021YJ0181)

The involvements of pyramidal neurons in ventromedial prefrontal cortex in the regulation of pain and anxiety-like behavior of spared nerve injury mice

Lin Peimin1, Liu Yan1, Liu Ting2, Yin Haoling2, Zhang Ying1*    

  1. 1. Department of  Anesthesiology, The Affiliated TCM Hospital of Southwest Medical University, Luzhou 646000, Sichuan Province, China; 2. Southwest Medical University, Luzhou 646000, Sichuan Province, China 
  • Received:2022-03-11 Online:2023-09-25 Published:2023-10-16

摘要: 目的    探究腹内侧前额叶皮质(ventromedial prefrontal cortex,vmPFC)锥体神经元对选择性坐骨神经损伤(spared nerve injury,SNI)小鼠疼痛和焦虑样行为的调控作用。  方法    构建SNI神经病理性疼痛(neuropathic pain,NP)动物模型,假手术组(sham)仅暴露神经。向SNI小鼠损伤对侧腹内侧前额叶皮质(ventromedial prefrontal cortex,vmPFC)注射红藻氨酸/生理盐水,或化学遗传学抑制病毒/空载对照病毒。采用von frey纤维丝检测SNI术后损伤侧机械缩足反射阈值(paw withdrawl threshold,PWT);高架十字迷宫评估SNI术后焦虑情况;免疫荧光染色观察SNI损伤对侧vmPFC中c-fos表达及注射红藻氨酸后神经元毁损、星形胶质细胞活化情况,RNA-scope原位杂交染色与免疫荧光染色双标明确Vgat基因和Vglut1基因分别与c-fos的共表达情况。  结果    术后7 d及14 d,相比于sham小鼠,SNI小鼠损伤侧足底PWT、进入开臂次数和停留时间明显减少(P<0.05);SNI小鼠损伤对侧vmPFC中c-fos阳性神经元数量明显增加,c-fos主要表达在Vglut1基因阳性的神经元(P<0.05)。相比于损伤对侧vmPFC注射生理盐水的SNI小鼠,注射红藻氨酸的SNI小鼠损伤对侧vmPFC中出现明显的神经元毁损及星形胶质细胞活化现象,损伤侧足底PWT、进入开臂次数和时间明显增加(P<0.05)。此外,化学遗传学策略抑制SNI小鼠损伤对侧vmPFC的锥体神经元后,SNI小鼠损伤对侧vmPFC中c-fos阳性神经元数量明显减少,同时损伤侧足底PWT、进入开臂次数和时间明显增加(P<0.05)。  结论    SNI小鼠损伤对侧vmPFC中的锥体神经元影响疼痛及焦虑样行为的发生发展。

关键词: 腹内侧前额叶皮质; ,  , 化学遗传学; ,  , 锥体神经元; ,  , 疼痛; ,  , 焦虑

Abstract: Objective    To explore the role of pyramidal neurons of ventromedial prefrontal cortex (vmPFC) in pain and anxiety-like behavior of spared nerve injury (SNI) mice.    Methods    Spared nerve injury (SNI) was used to mimic neuropathic pain (NP) animal model, while a same incision without nerve injury was performed to establish the sham control group. Kainic aicd, normal saline, AAV2/9 virus were intracranially injected into contralateral vmPFC of SNI mice. Von frey filaments were used to detect the paw withdraw threshold (PWT) of the ipsilateral planta of SNI mice. The elevated plus maze (EPM) was used to assess anxiety behaviors of SNI mice. Immunofluorescence staining was used to observe the expression of c-fos, the neuronal loss and the astrocytic activation in the contralateral vmPFC. RNA-scope and immunofluorescence staining were used to identify the neuronal type of c-fos positive neuron of vmPFC. Results    Compared with sham mice, ipsilateral PWT, entries in open arms and cumulative duration in open arms of SNI mice were significantly decreased at 7d and 14d after SNI (P<0.05). Compared with sham mice, c-fos positive neurons were significantly increased in the contralateral of vmPFC of SNI mice (P<0.05). In addition, the c-fos positive neurons were almost Vglut1 positive neurons. Compared with the SNI mice which intracranially injected into contraleral vmPFC with normal saline, ipsilateral PWT, entries in open arms and cumulative duration in open arms of the SNI mice which intracranially injected into contraleral vmPFC with kainic acid were increased (P<0.05). Meanwhile, the SNI mice which intracranially injected into contraleral vmPFC with kainic acid exhibited obvious neuronal loss and astrocytic activation in the contralateral vmPFC. In addition, using chemogenetics strategy to inhibit the pyramidal neurons in contralateral vmPFC of SNI mice, the c-fos positive neurons were significantly deceased, the ipsilateral PWT, entries in open arms and cumulative duration in open arms were significantly increased (P<0.05).    Conclusions    Pyramidal neurons in the contralateral vmPFC may be involved in the development of pain and anxiety-like behaviors of SNI mice.

Key words: Ventromedial prefrontal cortex; ,  , Chemogenetics; ,  , Pyramidal neuron; ,  , Pain; ,  , Anxiety

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