Zhang Li Ping, Chen Ying, Clark Barry P, Sher Emanuele, Westlund Karin N
Department of Anatomy and Neuroscience, Marine Biomedical Institute, The University of Texas Medical Branch at Galveston, Galveston, TX; and Eli Lilly and Co, Windlesham, Surrey, United Kingdom.
J Pain. 2000 Summer;1(2):151-161. doi: 10.1016/S1526-5900(00)90100-7.
Antidromically propagated action potentials can be recorded in the proximal end of the severed medial articular nerve (MAN) on mechanical stimulation of an inflamed knee in rats and are referred to as dorsal root reflex (DRR) activity. The absence of DRR activity in normal rats suggests that the activity could be the result of hyperexcitability of spinal neurons induced by inflammation. In this study, the role of spinal type 1 metabotropic glutamate (mGlu(1)) receptors in the generation of DRR activity in the MAN during acute knee inflammation was investigated. Four hours after an injection of a mixture of kaolin and carrageenan (k/c) into a knee joint, DRR activity could be evoked in the ipsilateral MAN by mechanical stimulation of the inflamed limb. Spinal application of a selective mGlu(1) receptor antagonist, [RS]-1-Aminoindan-1,5-dicarboxylic acid/UPF 523 (AIDA), or a potent, but less specific mGlu(1) receptor antagonist, LY393053, both depressed the DRR activity significantly. AIDA and LY39053 had no effect on recordings in the MAN from noninflamed control animals. However, spinal administration of AIDA did suppress DRR activity generated by infusion of 4-aminopyridine (4-AP), a K(+) channel blocker, into the dorsal horn of noninflamed animals. These observations suggest that mGlu(1) receptors support the generation of DRR activity in the MAN following sensitization of spinal cord neurons.
在对大鼠发炎的膝盖进行机械刺激时,可在切断的内侧关节神经(MAN)近端记录到逆向传播的动作电位,这被称为背根反射(DRR)活动。正常大鼠中不存在DRR活动,这表明该活动可能是由炎症诱导的脊髓神经元兴奋性过高所致。在本研究中,调查了脊髓I型代谢型谷氨酸(mGlu(1))受体在急性膝盖炎症期间MAN中DRR活动产生过程中的作用。向膝关节注射高岭土和角叉菜胶(k/c)混合物4小时后,通过对发炎肢体进行机械刺激可在同侧MAN中诱发DRR活动。脊髓应用选择性mGlu(1)受体拮抗剂[RS]-1-氨基茚满-1,5-二羧酸/UPF 523(AIDA)或强效但特异性较低的mGlu(1)受体拮抗剂LY393053,均能显著抑制DRR活动。AIDA和LY39053对未发炎对照动物的MAN记录无影响。然而,脊髓给予AIDA确实能抑制通过向未发炎动物的背角注射钾通道阻滞剂4-氨基吡啶(4-AP)所产生的DRR活动。这些观察结果表明,mGlu(1)受体在脊髓神经元致敏后支持MAN中DRR活动的产生。