Department of Neurosciences, School of Medicine and Dentistry, University of the Basque Country, 48080 Bilbao, Bizkaia, Spain.
J Neurosci. 2012 Sep 26;32(39):13568-81. doi: 10.1523/JNEUROSCI.1364-12.2012.
Emerging evidence implicates serotonergic descending facilitatory pathways from the brainstem to the spinal cord in the maintenance of pathologic pain. Upregulation of the serotonin receptor 2A (5-HT(2A)R) in dorsal horn neurons promotes spinal hyperexcitation and impairs spinal μ-opioid mechanisms during neuropathic pain. We investigated the involvement of spinal glutamate receptors, including metabotropic receptors (mGluRs) and NMDA, in 5-HT(2A)R-induced hyperexcitability after spinal nerve ligation (SNL) in rat. High-affinity 5-HT(2A)R agonist (4-bromo-3,6-dimethoxybenzocyclobuten-1-yl)methylamine hydrobromide (TCB-2) enhanced C-fiber-evoked dorsal horn potentials after SNL, which was prevented by mGluR1 antagonist AIDA [(RS)-1-aminoindan-1,5-dicarboxylic acid] but not by group II mGluR antagonist LY 341495 [(2S)-2-amino-2-[(1S,2S)-2-carboxycycloprop-1-yl]-3-(xanth-9-yl)propanoic acid] or NMDA antagonist d-AP5 [D-(-)-2-amino-5-phosphonopentanoic acid]. 5-HT(2A)R and mGluR1 were found to be coexpressed in postsynaptic densities in dorsal horn neurons. In the absence of SNL, pharmacological stimulation of 5-HT(2A)R with TCB-2 both induced rapid bilateral upregulation of mGluR1 expression in cytoplasmic and synaptic fractions of spinal cord homogenates, which was attenuated by PKC inhibitor chelerythrine, and enhanced evoked potentials during costimulation of mGluR1 with 3,5-DHPG [(RS)-3,5-dihydroxyphenylglycine]. SNL was followed by bilateral upregulation of mGluR1 in 5-HT(2A)R-containing postsynaptic densities. Upregulation of mGluR1 in synaptic compartments was partially prevented by chronic administration of selective 5-HT(2A)R antagonist M100907 [(R)-(+)-α-(2,3-dimethoxyphenyl)-1-[2-(4-fluorophenyl)ethyl]-4-pipidinemethanol], confirming 5-HT(2A)R-mediated control of mGluR1 upregulation triggered by SNL. Changes in thermal and mechanical pain thresholds following SNL were increasingly reversed over the days after injury by chronic 5-HT(2A)R blockade. These results emphasize a role for 5-HT(2A)R in hyperexcitation and pain after nerve injury and support mGluR1 upregulation as a novel feedforward activation mechanism contributing to 5-HT(2A)R-mediated facilitation.
越来越多的证据表明,脑干到脊髓的 5-羟色胺能下行易化通路在病理性疼痛的维持中起作用。背角神经元中 5-羟色胺受体 2A(5-HT(2A)R)的上调促进了神经病理性疼痛期间脊髓的过度兴奋,并损害了脊髓 μ-阿片机制。我们研究了脊髓谷氨酸受体,包括代谢型谷氨酸受体(mGluRs)和 NMDA,在大鼠脊髓神经结扎(SNL)后 5-HT(2A)R 诱导的过度兴奋中的作用。高亲和力 5-HT(2A)R 激动剂(4-溴-3,6-二甲氧基苯并环丁烯-1-基)甲胺氢溴酸盐(TCB-2)增强了 SNL 后的 C 纤维诱发的背角电位,该作用被 mGluR1 拮抗剂 AIDA [(RS)-1-氨基茚-1,5-二羧酸]而不是 II 组 mGluR 拮抗剂 LY 341495 [(2S)-2-氨基-2-[(1S,2S)-2-羧基环丙-1-基]-3-(黄嘌呤-9-基)丙氨酸]或 NMDA 拮抗剂 d-AP5 [D-(-)-2-氨基-5-膦戊酸]阻断。在背角神经元的突触后密度中发现 5-HT(2A)R 和 mGluR1 共表达。在没有 SNL 的情况下,用 TCB-2 对 5-HT(2A)R 的药理学刺激既诱导脊髓匀浆细胞质和突触部分中 mGluR1 表达的快速双侧上调,该上调被蛋白激酶 C 抑制剂 Chelerythrine 减弱,并且在 3,5-DHPG [(RS)-3,5-二羟基苯甘氨酸]与 mGluR1 共刺激期间增强了诱发的电位。SNL 后,5-HT(2A)R 包含的突触后密度中的 mGluR1 上调。选择性 5-HT(2A)R 拮抗剂 M100907 [(R)-(+)-α-(2,3-二甲氧基苯基)-1-[2-(4-氟苯基)乙基]-4-哌啶甲醇]的慢性给药部分阻止了突触间 mGluR1 的上调,证实了 5-HT(2A)R 介导的 SNL 触发的 mGluR1 上调的控制。SNL 后热痛和机械痛阈值的变化在损伤后几天内逐渐通过慢性 5-HT(2A)R 阻断得到逆转。这些结果强调了 5-HT(2A)R 在神经损伤后过度兴奋和疼痛中的作用,并支持 mGluR1 上调作为一种新的前馈激活机制,有助于 5-HT(2A)R 介导的易化。