Cameron Darren, Polgár Erika, Gutierrez-Mecinas Maria, Gomez-Lima Maria, Watanabe Masahiko, Todd Andrew J
Institute of Neuroscience and Psychology, College of Medical, Veterinary and Life Sciences, University of Glasgow, Glasgow, United Kingdom Department of Anatomy, Hokkaido University School of Medicine, Sapporo, Japan.
Pain. 2015 Oct;156(10):2061-2071. doi: 10.1097/j.pain.0000000000000270.
The anterolateral tract (ALT), which originates from neurons in lamina I and the deep dorsal horn, represents a major ascending output through which nociceptive information is transmitted to brain areas involved in pain perception. Although there is detailed quantitative information concerning the ALT in the rat, much less is known about this system in the mouse, which is increasingly being used for studies of spinal pain mechanisms because of the availability of genetically modified lines. The aim of this study was therefore to determine the extent to which information about the ALT in the rat can be extrapolated to the mouse. Our results suggest that as in the rat, most lamina I ALT projection neurons in the lumbar enlargement can be retrogradely labelled from the lateral parabrachial area, that the majority of these cells (∼ 90%) express the neurokinin 1 receptor (NK1r), and that these are larger than other NK1r-expressing neurons in this lamina. This means that many lamina I spinoparabrachial cells can be identified in NK1r-immunostained sections from animals that have not received retrograde tracer injections. However, we also observed certain species differences, in particular we found that many spinoparabrachial cells in laminae III and IV lack the NK1r, meaning that they cannot be identified based solely on the expression of this receptor. We also provide evidence that the majority of spinoparabrachial cells are glutamatergic and that some express substance P. These findings will be important for studies designed to unravel the complex neuronal circuitry that underlies spinal pain processing.
前外侧束(ALT)起源于I层和背角深层的神经元,是一条主要的上行传出通路,伤害性信息通过该通路传递至参与疼痛感知的脑区。尽管有关于大鼠ALT的详细定量信息,但对于小鼠的这个系统却知之甚少,由于转基因品系的可用性,小鼠越来越多地被用于脊髓疼痛机制的研究。因此,本研究的目的是确定大鼠ALT的信息能在多大程度上外推至小鼠。我们的结果表明,与大鼠一样,腰膨大处的大多数I层ALT投射神经元可被来自外侧臂旁核区域的逆行标记,这些细胞中的大多数(约90%)表达神经激肽1受体(NK1r),且这些细胞比该层中其他表达NK1r的神经元更大。这意味着在未接受逆行示踪剂注射的动物的NK1r免疫染色切片中可以识别出许多I层脊髓臂旁细胞。然而,我们也观察到了某些种属差异,特别是我们发现III层和IV层中的许多脊髓臂旁细胞缺乏NK1r,这意味着不能仅基于该受体的表达来识别它们。我们还提供了证据表明大多数脊髓臂旁细胞是谷氨酸能的,并且一些表达P物质。这些发现对于旨在揭示脊髓疼痛处理基础的复杂神经元回路的研究将具有重要意义。