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Differential innervation of superficial versus deep laminae of the dorsal horn by bulbo-spinal serotonergic pathways in the rat

机译:大鼠球根-脊髓血清素能通路对背角浅层与深层的差异神经支配

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摘要

Convergent data showed that bulbo-spinal serotonergic projections exert complex modulatory influences on nociceptive signaling within the dorsal horn. These neurons are located in the B3 area which comprises the median raphe magnus (RMg) and the lateral paragigantocellular reticular (LPGi) nuclei. Because LPGi 5-HT neurons differ from RMg 5-HT neurons regarding both their respective electrophysiological properties and responses to noxious stimuli, we used anatomical approaches for further characterization of the respective spinal projections of LPGi versus RMg 5-HT neuron subgroups.Adult Sprague-Dawley rats were stereotaxically injected into the RMg or the LPGi with the anterograde tracer Phaseolus vulgaris leucoagglutinin (PHA-L). The precise location of injection sites and RMg vs LPGi spinal projections into the different dorsal horn laminae were visualized by PHA-L immunolabeling. Double immunofluorescent labeling of PHA-L and the serotonin transporter (5-HTT) allowed detection of serotonergic fibers among bulbo-spinal projections.Anterograde tracing showed that RMg neurons project preferentially into the deep laminae V-VI whereas LPGi neuron projections are confined to the superficial laminae I-II of the ipsilateral dorsal horn. All along the spinal cord, double-labeled PHA-L/5-HTT immunoreactive fibers, which represent only 5–15% of all PHA-L-immunoreactive projections, exhibit the same differential locations depending on their origin in the RMg versus the LPGi.The clear-cut distinction between dorsal horn laminae receiving bulbo-spinal serotonergic projections from the RMg versus the LPGi provides further anatomical support to the idea that the descending serotonergic pathways issued from these two bulbar nuclei might exert different modulatory influences on the spinal relay of pain signaling neuronal pathways.
机译:汇聚的数据表明,球鼻脊髓血清素能投射对背角内的伤害性信号传导产生复杂的调节作用。这些神经元位于B3区域,该区域包括正中缝大核(RMg)和旁巨细胞网状(LPGi)核。由于LPGi 5-HT神经元在其各自的电生理特性和对有害刺激的反应方面均不同于RMg 5-HT神经元,因此我们使用解剖学方法进一步表征了LPGi与RMg 5-HT神经元亚组的各自脊柱投射。将Dawley大鼠与顺行示踪剂菜豆白斑凝集素(PHA-L)立体定向注射到RMg或LPGi中。通过PHA-L免疫标记可以观察到注射部位的精确位置以及RMg vs LPGi脊柱突入不同背角薄片的位置。 PHA-L和5-羟色胺转运蛋白(5-HTT)的双重免疫荧光标记可检测出球茎突突中的血清素能纤维。顺行示踪显示,RMg神经元优先突入深层V-VI,而LPGi神经元突入限定于肺突突。同侧背角的浅层I-II。在整个脊髓中,双重标记的PHA-L / 5-HTT免疫反应性纤维(仅占所有PHA-L免疫反应性投射的5–15%)根据它们在RMg和LPGi中的起源表现出相同的不同位置。从RMg与LPGi接收球根-脊髓血清素能投射的背角椎板之间的明显区别为以下观点提供了进一步的解剖学支持:由这两个球根核发出的下降的血清素能途径可能对大鼠的脊髓中继产生不同的调节影响。疼痛信号传导神经元通路。

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