小胶质细胞
兴奋剂
米诺环素
医学
炎症体
受体
药理学
内分泌学
CX3CR1型
内科学
炎症
化学
生物化学
趋化因子
趋化因子受体
抗生素
作者
Qi Zhang,Qingchun Li,Siying Liu,Hangping Zheng,Lijin Ji,Na Yi,Weiqi Bao,Xiaoming Zhu,Wanwan Sun,Xiaoxia Liu,Shuo Zhang,Chuantao Zuo,Yiming Li,Qian Xiong,Bin Lü
标识
DOI:10.1016/j.diabres.2022.109806
摘要
We aimed to explore the evidence of brain microglia activation in diabetic neuropathic pain (DNP) and the effect and mechanism of glucagon-like peptide-1 receptor agonist (GLP-RA) on DNP via brain microglia.Brain microglia activation was observed in DNP rats by positron emission tomography/computed tomography. The behavior of neuropathic pain was assessed in DNP rats after intracerebroventricular administration of GLP-1RA or microglial inhibitor minocycline. RNA sequencing was performed to explore the target of GLP-1RA on brain microglia. NOD-like receptor protein 3 (NLRP3) expression in brain microglia was evaluated in mentioned-above DNP rats, and the activation of NLRP3 inflammasome was analyzed in microglia treated with GLP-1RA.Microglia were activated in the cortex and thalamus of DNP rats. The thermal and mechanical allodynia were alleviated in DNP rats via intracerebroventricular administration of GLP-1RA or minocycline. And the activation of brain microglia was attenuated in DNP rats by intracerebroventricular administration of GLP-1RA. The expression of NLRP3 in brain microglia, which was found by RNA sequencing, was reduced in DNP rats by administration of GLP-1RA. Furthermore, GLP-1RA attenuated NLRP3 inflammasome activation in microglia triggered by LPS.GLP-1RA could alleviate DNP, possibly mediated by the suppression of brain microglia NLRP3 inflammasome activation.
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