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背角内的楔束内脏传入投射神经元形成不同的细胞群。

Spinoparabrachial projection neurons form distinct classes in the mouse dorsal horn.

机构信息

School of Biomedical Sciences and Pharmacy, Faculty of Health, University of Newcastle, Callaghan, New South Wales, Australia.

Hunter Medical Research Institute (HMRI), New Lambton Heights, New South Wales, Australia.

出版信息

Pain. 2021 Jul 1;162(7):1977-1994. doi: 10.1097/j.pain.0000000000002194.

Abstract

Projection neurons in the spinal dorsal horn relay sensory information to higher brain centres. The activation of these populations is shaped by afferent input from the periphery, descending input from the brain, and input from local interneuron circuits. Much of our recent understanding of dorsal horn circuitry comes from studies in transgenic mice; however, information on projection neurons is still based largely on studies in monkey, cat, and rat. We used viral labelling to identify and record from mouse parabrachial nucleus (PBN) projecting neurons located in the dorsal horn of spinal cord slices. Overall, mouse lamina I spinoparabrachial projection neurons (SPBNs) exhibit many electrophysiological and morphological features that overlap with rat. Unbiased cluster analysis distinguished 4 distinct subpopulations of lamina I SPBNs, based on their electrophysiological properties that may underlie different sensory signalling features in each group. We also provide novel information on SPBNs in the deeper lamina (III-V), which have not been previously studied by patch clamp analysis. These neurons exhibited higher action potential discharge frequencies and received weaker excitatory synaptic input than lamina I SPBNs, suggesting this deeper population produces different sensory codes destined for the PBN. Mouse SPBNs from both regions (laminae I and III-V) were often seen to give off local axon collaterals, and we provide neuroanatomical evidence they contribute to excitatory input to dorsal horn circuits. These data provide novel information to implicate excitatory input from parabrachial projection neuron in dorsal horn circuit activity during processing of nociceptive information, as well as defining deep dorsal horn projection neurons that provide an alternative route by which sensory information can reach the PBN.

摘要

脊髓背角中的投射神经元将感觉信息传递到大脑高级中枢。这些神经元群体的激活受到来自外周的传入输入、来自大脑的下行输入以及来自局部中间神经元回路的输入的影响。我们对背角回路的最新理解大部分来自于转基因小鼠的研究;然而,关于投射神经元的信息仍然主要基于猴、猫和大鼠的研究。我们使用病毒标记来识别和记录位于脊髓切片背角中的小鼠臂旁核(PBN)投射神经元。总的来说,小鼠 I 层脊髓-臂旁核投射神经元(SPBNs)表现出许多与大鼠重叠的电生理和形态特征。基于其电生理特性的无偏聚类分析将 I 层 SPBNs 分为 4 个不同的亚群,这可能是每个亚群中不同感觉信号特征的基础。我们还提供了关于深层(III-V 层)SPBNs 的新信息,这些信息以前没有通过膜片钳分析进行研究。这些神经元表现出更高的动作电位放电频率,并且接收到的兴奋性突触输入比 I 层 SPBNs 弱,这表明这个更深层的神经元群体产生了不同的感觉编码,这些感觉编码将被传递到臂旁核。来自这两个区域(I 层和 III-V 层)的小鼠 SPBNs 经常被观察到发出局部轴突侧支,我们提供了神经解剖学证据表明它们对背角回路的兴奋性输入有贡献。这些数据提供了新的信息,表明来自臂旁核投射神经元的兴奋性输入参与了伤害感受信息处理过程中的背角回路活动,并定义了深部背角投射神经元,它们提供了一种替代途径,使感觉信息能够到达臂旁核。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6354/8208100/9c2883d586a1/jop-162-1977-g001.jpg

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