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首页> 外文期刊>Journal of pharmacological sciences. >Presynaptic inhibitory effects of fluvoxamine, a selective serotonin reuptake inhibitor, on nociceptive excitatory synaptic transmission in spinal superficial dorsal horn neurons of adult mice
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Presynaptic inhibitory effects of fluvoxamine, a selective serotonin reuptake inhibitor, on nociceptive excitatory synaptic transmission in spinal superficial dorsal horn neurons of adult mice

机译:氟异种胺,一种选择性血清素再摄取抑制剂的突触抑制作用,对成年小鼠脊髓性肾脏骨质背角神经元的伤害兴奋性突触透析

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Fluvoxamine, a selective serotonin (5-HT) reuptake inhibitor, has been shown to exert analgesic effects in humans and laboratory animals. However, its effects on spinal nociceptive synaptic transmission have not been fully characterized. Here, whole-cell recordings were made from dorsal horn neurons in spinal slices with attached dorsal roots from adult mice, and the effects of fluvoxamine on monosynaptic A-fiber- and C-fiber-mediated excitatory postsynaptic currents (EPSCs) evoked in response to electrical stimulation of a dorsal root were studied. Fluvoxamine (10 - 100 μM) concentration-dependently suppressed both monosynaptic A-fiber-and C-fiber-mediated EPSCs, which were attenuated by the selective 5-HT1A receptor antagonist WAY100635. In the presence of the selective 5-HT3 receptor antagonist tropisetron, fluvoxamine hardly suppressed A-fiber-mediated EPSCs, whereas its inhibitory effect on C-fiber-mediated EPSCs was not affected. Although fluvoxamine increased the paired-pulse ratio of A-fiber-mediated EPSCs, it increased the frequency of spontaneous and miniature EPSCs (sEPSCs and mEPSCs). Since sEPSCs and mEPSCs appeared to arise largely from spinal interneurons, we then recorded strontium-evoked asynchronous events occurring after A-fiber stimulation, whose frequency was reduced by fluvoxamine. These results suggest that fluvoxamine reduces excitatory synaptic transmission from primary afferent fibers via presynaptic mechanisms involving 5-HT1A and/or 5-HT3 receptors, which may contribute to its analgesic effects.
机译:氟异种胺是一种选择性血清素(5-HT)再摄取抑制剂,已显示在人类和实验室动物中施加镇痛作用。然而,它对脊柱伤害突触传递的影响尚未完全表征。在这里,全部细胞记录由脊椎切片中的背角神经元制成,其中来自成人小鼠的附着背根,以及氟戊胺对响应的单次突触性A-纤维和C-纤维介导的兴奋性突触激发(EPSCs)的影响。研究了背根的电刺激。氟诺胺(10-100μm)浓度依赖性抑制了单腹部A-纤维和C-纤维介导的EPSC,其被选择性5-HT1A受体拮抗剂Way100635衰减。在选择性5-HT3受体拮抗剂对象棘轮的存在下,氟戊胺几乎没有抑制A-纤维介导的EPSC,而其对C-纤维介导的EPSCs的抑制作用不受影响。诸如氟酚胺增加了A-纤维介导的EPSC的配对脉冲比,但它增加了自发性和微型EPSCs(SEPSCS和MEPSCs)的频率。由于SEPSCS和MEPSCS似乎主要来自脊柱间核,因此我们在纤维刺激后记录了锶诱发的异步事件,其频率通过FluVoxamine降低。这些结果表明,氟异种胺通过涉及5-HT1A和/或5-HT3受体的突触前机制从初级传入纤维中减少了初级传入纤维的兴奋性突触传递,这可能有助于其镇痛作用。

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