The inhibiting role of periaqueductal gray metabotropic glutamate receptor subtype 8 in a rat model of central neuropathic pain

被引:7
|
作者
Hosseini, Marjan [1 ]
Parviz, Mohsen [1 ]
Shabanzadeh, Alireza P. [1 ]
Zamani, Elham [1 ]
Mohseni-Moghaddam, Parvaneh [1 ]
Gholami, Leila [1 ]
Mehrabadi, Shima [1 ]
机构
[1] Univ Tehran Med Sci, Sch Med, Dept Physiol, Tehran, Iran
关键词
mGlur8; central neuropathic pain; spinal cord injury; periaqueductal Gray; allodynia; ACID RELEASE; CELLS; AMYGDALA; INJURY;
D O I
10.1080/01616412.2020.1747730
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
The pathophysiology of neuropathic pain is very complex. It involves several environmental and central mechanisms. In this study, we tried to assess the modulatory effect of (S)-3,4-Dicarboxyphenylglycine (DCPG), a metabotropic glutamate receptor subtype 8 (mGluR8) agonist, in a model of chronic central neuropathic pain in male rats. We used a spinal cord contusion method (T6-T8) for the induction of chronic central neuropathic pain. Male Wistar rats were randomly assigned to 5 equal groups (n = 10 per group). Clips compression injury model was used to induce chronic central neuropathic pain. Three weeks after spinal cord injury DCPG, siRNA and normal saline were administered intra-ventrolaterally to the periaqueductal gray (PAG) region. Paw withdrawal response to acetone (cold allodynia) was assessed through acetone test. In addition, the effects of DCPG on rostral ventromedial medulla (RVM) off-cells activity were evaluated with immunohistochemistry. mGluR8 expressions were also measured. We found that treatment with DCPG increased pain threshold in acetone test. In addition, immunohistochemical evaluation of RVM off-cells showed that DCPG increased the suppressive function of these cells. The results revealed that activation of mGluR8 in PAG is capable to improve pain threshold via modulation of RVM off-cells activity.
引用
收藏
页码:515 / 521
页数:7
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