Orthopedics Department, Huzhou Central Hospital, 198 Hongqi Road, Huzhou 313000, People's Republic of China.
Neurosci Lett. 2012 Nov 30;531(1):52-6. doi: 10.1016/j.neulet.2012.10.014. Epub 2012 Oct 17.
Group II and III metabolic glutamate receptors (mGluRs) are responsible for the glutamate-mediated postsynaptic excitation of neurons. Previous pharmacological evidences show that activation of mGluR7 could inhibit nociceptive reception. However, the distribution and expression patterns of mGluR7 after peripheral injury remain unclear. Herein we found that mGluR7 was expressed in the rat peptidergic dorsal root ganglion (DRG) neurons and large neurons, but rarely in isolectin B4 positive neurons. Sciatic nerve ligation experiment showed that mGluR7 was anterogradely transported from cell body to the peripheral site. Furthermore, after peripheral nerve injury, mGluR7 expression was down-regulated in both peptidergic and large DRG neurons. Our work suggests that mGluR7 might be involved in the regulation of pathological pain after peripheral nerve injury.
II 类和 III 类代谢型谷氨酸受体(mGluRs)负责神经元的谷氨酸能突触后兴奋。先前的药理学证据表明,mGluR7 的激活可以抑制伤害性感受。然而,外周损伤后 mGluR7 的分布和表达模式仍不清楚。本文发现,mGluR7 在大鼠肽能背根神经节(DRG)神经元和大神经元中表达,但在异硫氰酸荧光素 B4 阳性神经元中很少表达。坐骨神经结扎实验表明,mGluR7 从细胞体顺行运输到外周部位。此外,外周神经损伤后,肽能和大 DRG 神经元中的 mGluR7 表达均下调。我们的工作表明,mGluR7 可能参与外周神经损伤后的病理性疼痛调节。