State Key Laboratory of Medical Neurobiology and Institutes of Brain Science, Fudan University, 138 Yi Xue Yuan Road, Shanghai 200032, China.
Pain. 2010 Mar;148(3):414-425. doi: 10.1016/j.pain.2009.11.025. Epub 2009 Dec 24.
High density Nociceptin/Orphanin FQ (N/OFQ) and its receptor (NOPr) have been found in the ventrolateral periaqueductal gray (vlPAG), a main output pathway involved in the descending pain-control system. Our previous study demonstrated that the microinjection of N/OFQ into the vlPAG markedly facilitated nociceptive responses of spinal dorsal horn neurons. The aim of the present work was to further provide evidence for the supraspinal mechanisms of action for N/OFQ-mediated nociceptive facilitation by examining the effect of N/OFQ in the vlPAG on neurotransmitter release in the descending pain-control system, including the nucleus raphe magnus (NRM), nucleus reticularis gigantocellularis (NGC) and dorsal horn of the spinal cord. The results showed that the microinjection of N/OFQ into the vlPAG produced robust decreases in 5-hydroxytryptamine (5-HT, serotonin), norepinephrine (NE), and gamma-aminobutyric acid (GABA), and increase in glutamate (Glu) release in the spinal dorsal horn. Spinal application of 5-HT, 2-Me-5-HT (5-HT(3) receptor agonist), muscimol (GABA(A) receptor agonist), and baclofen (GABA(B) receptor agonist) significantly blocked intra-vlPAG-induced facilitation on nociceptive responses. However, the extracellular concentrations of these neurotransmitters in the NRM and NGC exhibited diversity following intra-vlPAG of N/OFQ. In the NRM, intra-vlPAG injection of N/OFQ significantly decreased 5-HT, NE, and Glu, but increased GABA release. Differently, in the NGC, both NE and GABA releases were attenuated by intra-vlPAG of N/OFQ, whereas the concentration of 5-HT and Glu exhibited a trend to increase. These findings provide direct support for the hypothesis that intra-PAG of N/OFQ-induced facilitation of nociceptive responses is associated with the release of 5-HT, NE, and amino acids.
高密度孤啡肽/孤啡肽受体(N/OFQ/NOPr)存在于腹外侧导水管周围灰质(vlPAG)中,这是参与下行疼痛控制系统的主要输出途径。我们之前的研究表明,将 N/OFQ 注射到 vlPAG 中会明显促进脊髓背角神经元的伤害性反应。本研究的目的是通过检查 N/OFQ 在 vlPAG 中对下行疼痛控制系统中神经递质释放的影响,进一步为 N/OFQ 介导的伤害性易化的中枢机制提供证据,包括中缝大核(NRM)、巨细胞网状核(NGC)和脊髓背角。结果表明,将 N/OFQ 注射到 vlPAG 中会导致脊髓背角 5-羟色胺(5-HT,血清素)、去甲肾上腺素(NE)和γ-氨基丁酸(GABA)的释放显著减少,谷氨酸(Glu)的释放增加。脊髓应用 5-HT、2-Me-5-HT(5-HT3 受体激动剂)、muscimol(GABA(A)受体激动剂)和 baclofen(GABA(B)受体激动剂)显著阻断了 intra-vlPAG 诱导的伤害性反应的易化作用。然而,N/OFQ 注入 vlPAG 后,NRM 和 NGC 中这些神经递质的细胞外浓度表现出多样性。在 NRM 中,vlPAG 内注射 N/OFQ 显著降低 5-HT、NE 和 Glu,但增加 GABA 释放。相反,在 NGC 中,N/OFQ 注入后 NE 和 GABA 的释放均减弱,而 5-HT 和 Glu 的浓度呈增加趋势。这些发现为 N/OFQ 诱导的 PAG 内伤害性反应的易化与 5-HT、NE 和氨基酸的释放有关的假说提供了直接支持。