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激活腹外侧水管周围灰质中表达 CamKIIα 的神经元可改善三叉神经痛大鼠模型中的行为过敏和丘脑放电。

Activation of CamKIIα expressing neurons on ventrolateral periaqueductal gray improves behavioral hypersensitivity and thalamic discharge in a trigeminal neuralgia rat model.

机构信息

Department of Neuroscience, College of Medicine, Chungbuk National University, Cheongju, South Korea.

Department of Neurosurgery, Chungbuk National University Hospital, Cheongju, South Korea.

出版信息

J Headache Pain. 2021 May 27;22(1):47. doi: 10.1186/s10194-021-01257-z.

Abstract

BACKGROUND

Preceding studies have reported the association of chronic neuropathic orofacial pain with altered ongoing function in the ventrolateral periaqueductal gray (vlPAG). However, its role in trigeminal neuralgia (TN) lacks attention. We here reported the aspect that vlPAG neurons play in TN nociceptive processing by employing excitatory neuron-specific optogenetic approaches.

METHODS

TN was generated via unilateral infraorbital nerve chronic constriction in Sprague Dawley rats which induced mechanical and thermal pain sensitivity in air puff and acetone test, respectively. Channelrhodopsin conjugated virus with CamKIIα promoter was used to specifically activate the excitatory vlPAG neuronal population by optogenetic stimulation and in vivo microdialysis was done to determine its effect on the excitatory-inhibitory balance. In vivo extracellular recordings from ventral posteromedial (VPM) thalamus were assessed in response to vlPAG optogenetic stimulation. Depending on the experimental terms, unpaired student's t test and two-way analysis of variance (ANOVA) were used for statistical analysis.

RESULTS

We observed that optogenetic activation of vlPAG subgroup neurons markedly improved pain hypersensitivity in reflexive behavior tests which was also evident on microdialysis analysis with increase glutamate concentration during stimulation period. Decreased mean firing and burst rates were evident in VPM thalamic electrophysiological recordings during the stimulation period. Overall, our results suggest the optogenetic activation of vlPAG excitatory neurons in a TN rat model has pain ameliorating effect.

CONCLUSIONS

This article presents the prospect of pain modulation in trigeminal pain pathway via optogenetic activation of vlPAG excitatory neurons in rat model. This outlook could potentially assist vlPAG insight and its optogenetic approach in trigeminal neuropathic pain which aid clinicians endeavoring towards enhanced pain relief therapy in trigeminal neuralgia patients.

摘要

背景

先前的研究报告称,慢性神经性或口腔面部疼痛与腹外侧导水管周围灰质(vlPAG)的持续功能改变有关。然而,其在三叉神经痛(TN)中的作用尚未得到关注。我们通过采用兴奋性神经元特异性光遗传学方法,报道了 vlPAG 神经元在 TN 伤害性处理中的作用。

方法

通过单侧眶下神经慢性缩窄在 Sprague Dawley 大鼠中产生 TN,这分别导致空气喷击和丙酮测试中的机械和热痛敏。带有 CamKIIα 启动子的通道视紫红质病毒用于通过光遗传学刺激特异性激活兴奋性 vlPAG 神经元群体,并进行体内微透析以确定其对兴奋性-抑制性平衡的影响。评估对 vlPAG 光遗传学刺激的腹后内侧(VPM)丘脑的体内细胞外记录。根据实验条件,使用未配对学生 t 检验和双向方差分析(ANOVA)进行统计分析。

结果

我们观察到,vlPAG 亚群神经元的光遗传学激活显着改善了反射行为测试中的疼痛敏感性,在刺激期间谷氨酸浓度增加的微透析分析中也很明显。在刺激期间,VPM 丘脑电生理记录中的平均放电和爆发率显着降低。总的来说,我们的结果表明,在 TN 大鼠模型中,vlPAG 兴奋性神经元的光遗传学激活具有缓解疼痛的作用。

结论

本文提出了通过光遗传学激活大鼠模型中 vlPAG 兴奋性神经元来调节三叉神经疼痛通路的疼痛的前景。这种观点可能有助于了解 vlPAG 及其在三叉神经病理性疼痛中的光遗传学方法,这有助于临床医生努力为三叉神经痛患者提供更好的疼痛缓解治疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e483/8161973/80c96521ae0d/10194_2021_1257_Fig1_HTML.jpg

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