香草素受体vr1阳性的初级传入是谷氨酸能和接触性脊髓神经元,它们共同表达神经激肽受体NK1和谷氨酸受体。

Se Jin Hwang, Alain Burette, Aldo Rustioni, Juli G Valtschanoff
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引用次数: 0

摘要

香草素受体VR1 (TRPV1)是一种对温度和辣椒素敏感的阳离子通道,由一类参与伤害感觉的初级传入事件表达。为了证实VR1阳性的初级传入是表达主要类型的嗜离子性谷氨酸受体的谷氨酸能和接触性脊髓神经元的假设,我们对VR1和谷氨酸转运体VGLUT2(谷氨酸能传递的特异性标记)或AMPA和NMDA受体亚基进行了多次免疫荧光染色。vr1阳性的背根神经节细胞及其背角中枢传入纤维钮扣表达VGLUT2,后者接触AMPA-或NMDA受体阳性的核周。基于我们之前对vr1阳性初级传入信号优先靶向表达神经激肽受体NK1的脊髓神经元的观察(Hwang et al., 2003),我们进一步量化了vr1阳性传入信号终止到共表达谷氨酸受体的NK1阳性神经元的频率。vr1阳性钮扣接触NK1/NMDA受体阳性位点的比例大于NK1/AMPA受体阳性位点。我们得出结论,vr1阳性的大鼠初级传入使用谷氨酸作为神经递质,并接触共同表达NK1和嗜离子性谷氨酸受体的突触后位点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Vanilloid receptor VR1-positive primary afferents are glutamatergic and contact spinal neurons that co-express neurokinin receptor NK1 and glutamate receptors.

The vanilloid receptor VR1 (TRPV1) is a temperature- and capsaicin-sensitive cation channel expressed by a class of primary afferents involved in nociception. To confirm the hypothesis that VR1-positive primary afferents are glutamatergic and contact spinal neurons that express the main classes of ionotropic glutamate receptors, we performed multiple immunofluorescent staining for VR1 and the glutamate transporter VGLUT2 (a specific marker for glutamatergic transmission) or AMPA and NMDA receptor subunits. VR1-positive cells in the dorsal root ganglion and boutons of their central afferent fibers in the dorsal horn expressed VGLUT2, and the latter contacted AMPA- or NMDA receptor-positive perikarya. Based on our previous observations of preferential targeting of VR1-positive primary afferents to spinal neurons that express the neurokinin receptor NK1 (Hwang et al., 2003), we further quantified the frequency of termination of VR1-positive afferents onto NK1-positive neurons co-expressing glutamate receptors. A larger fraction of NK1/NMDA receptors-positive than NK1/AMPA receptors-positive sites were contacted by VR1-positive boutons. We conclude that VR1-positive primary afferents in the rat use glutamate as neurotransmitter and contact postsynaptic sites that co-express NK1 and ionotropic glutamate receptors.

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