首页> 外文OA文献 >Projection neurons in lamina III of the rat spinal cord are\ud selectively innervated by local dynorphin-containing\ud excitatory neurons
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Projection neurons in lamina III of the rat spinal cord are\ud selectively innervated by local dynorphin-containing\ud excitatory neurons

机译:大鼠脊髓的III层中的投射神经元是\ n 由含有本地强啡肽的选择性神经支配 兴奋性神经元

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摘要

Large projection neurons in lamina III of the rat spinal cord that express the neurokinin 1 receptor are densely innervated by peptidergic primary afferent nociceptors and more sparsely by low-threshold myelinated afferents. However, we know little about their input from other glutamatergic neurons. Here we show that these cells receive numerous contacts from nonprimary boutons that express the vesicular glutamate transporter 2 (VGLUT2), and form asymmetrical synapses on their dendrites and cell bodies. These synapses are significantly smaller than those formed by peptidergic afferents, but provide a substantial proportion of the glutamatergic synapses that the cells receive (over a third of those in laminae I–II and half of those in deeper laminae). Surprisingly, although the dynorphin precursor preprodynorphin (PPD) was only present in 4–7% of VGLUT2 boutons in laminae I–IV, it was found in 58% of the VGLUT2 boutons that contacted these cells. This indicates a highly selective targeting of the lamina III projection cells by glutamatergic neurons that express PPD, and these are likely to correspond to local neurons (interneurons and possibly projection cells). Since many PPD-expressing dorsal horn neurons respond to noxious stimulation, this suggests that the lamina III projection cells receive powerful monosynaptic and polysynaptic nociceptive input. Excitatory interneurons in the dorsal horn have been shown to possess IA currents, which limit their excitability and can underlie a form of activity-dependent intrinsic plasticity. It is therefore likely that polysynaptic inputs to the lamina III projection neurons are recruited during the development of chronic pain states.
机译:表达神经激肽1受体的大鼠脊髓III层中的大型投射神经元被肽能的初级传入伤害感受器密集地支配,而低阈值的髓鞘传入感受器则稀疏地支配。但是,我们对其他谷氨酸能神经元的输入知之甚少。在这里,我们显示了这些细胞从表达水泡谷氨酸转运蛋白2(VGLUT2)的非主要弹子中接收大量接触,并在其树突和细胞体上形成不对称突触。这些突触明显小于肽能传入形成的突触,但提供了细胞所接收的谷氨酸能突触的相当一部分(超过层I–II中的三分之一,而更深层中的一半)。出人意料的是,尽管强啡肽前体强啡肽原(PPD)仅存在于I-IV层的VGLUT2钮扣的4–7%,但在与这些细胞接触的VGLUT2钮扣的58%中被发现。这表明表达PPD的谷氨酸能神经元高度选择性地靶向了层状III投射细胞,这些可能对应于局部神经元(中间神经元,可能还有投射细胞)。由于许多表达PPD的背角神经元对伤害性刺激作出反应,因此表明层板III投射细胞接受强大的单突触和多突触伤害性输入。背角中的兴奋性中间神经元已显示出具有IA电流,这限制了它们的兴奋性,并可能构成一种依赖于活动的固有可塑性。因此,有可能在慢性疼痛状态的发展期间募集了对层板III投射神经元的多突触输入。

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