P2X4 Receptors of Microglia in Neuropathic Pain

被引:21
|
作者
Inoue, Kazuhide [1 ]
Tsuda, Makoto [1 ]
机构
[1] Kyushu Univ, Grad Sch Pharmaceut Sci, Dept Mol & Syst Pharmacol, Higashi Ku, Fukuoka 8128582, Japan
关键词
P2X4Rs; microglia; neuropathic pain; PERIPHERAL-NERVE INJURY; ACTIVATED PROTEIN-KINASE; SPINAL-CORD MICROGLIA; UP-REGULATION; P2X(4) RECEPTORS; INTERNATIONAL UNION; TACTILE ALLODYNIA; NEURONAL CCL21; EXPRESSION; MECHANISMS;
D O I
10.2174/187152712803581065
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
We have learned various data on the role of purinoceptors (P2X4, P2X7, P2Y6 and P2Y12 receptors) expressed in spinal microglia and several factors that presumably activate microglia in neuropathic pain after peripheral nerve injury. Especially P2X4 receptors (P2X4Rs) make a critical contribution to the pain processing. P2X4Rs of microglia might be promising targets for treating neuropathic pain. A predicted therapeutic benefit of interfering with microglial P2X4Rs may be that normal pain sensitivity would be unaffected since expression or activity of most of these receptors are upregulated or enhanced predominantly in activated microglia in the spinal cord where damaged sensory fibers project. Recently, we found that CCL21 regulates the expression of P2X4Rs in different manners, respectively. These new findings also provide novel targets for developing anti-neuropathic pain medicines.
引用
收藏
页码:699 / 704
页数:6
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