A Critical Involvement of Glutamatergic Neurons in the Anterior Insular Cortex for Subdiaphragmatic Vagotomy-induced Analgesia

被引:2
|
作者
Kim, Yea Jin [1 ]
Lee, Grace J. [1 ]
Shim, Sang Wook [1 ]
Kim, Doyun [2 ]
Oh, Seog Bae [1 ,2 ,3 ]
机构
[1] Seoul Natl Univ, Coll Nat Sci, Dept Brain & Cognit Sci, Seoul 03080, South Korea
[2] Seoul Natl Univ, Tooth Periodontium Complex Med Res Ctr, Sch Dent, Seoul 03080, South Korea
[3] Seoul Natl Univ, Dent Res Inst, Sch Dent, Dept Neurobiol & Physiol, Seoul 03080, South Korea
基金
新加坡国家研究基金会;
关键词
Subdiaphragmatic vagotomy (SDV); Acute inflammatory pain; Anterior insular cortex; Glutamatergic neuron; VAGAL AFFERENTS; VAGUS NERVE; ELECTRICAL-STIMULATION; PAIN; MODULATION; MECHANISMS; RATS; ANTINOCICEPTION; EXCITABILITY; ACTIVATION;
D O I
10.5607/en23002
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Subdiaphragmatic vagotomy (SDV) is known to produce analgesic effect in various pain conditions including not only visceral pain but also so-matic pain. We aimed to determine brain mechanisms by which SDV induces analgesic effect in somatic pain condition by using formalin-induced acute inflammatory pain model. We identified brain regions that mediate SDV-induced analgesic effect on acute inflammatory pain by analyzing Fos expression in the whole brain. We found that c-Fos expression was specifically increased in the anterior insular cortex (aIC) among subregions of the insular cortex in acute inflammatory pain, which was reversed by SDV. These results were not mimicked in female mice, indicating sexual dimorphism in SDV-induced analgesia. SDV decreased c-Fos expressions more preferentially in glutamatergic neurons rather than GABAergic neurons in the aIC, and pharmacological activation of glutamatergic neurons with NMDA in the aIC inhibited SDV-induced analgesic effect. Fur-thermore, chemogenetic activation of glutamatergic neurons in the aIC reversed SDV-induced analgesia. Taken together, our results suggest that the decrease in the neuronal activity of glutamatergic neurons in the aIC mediates SDV-induced analgesic effect, potentially serving as an important therapeutic target to treat inflammatory pain.
引用
收藏
页码:68 / 82
页数:15
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