Spencer Nick J, Greenheigh Sarah, Kyloh Melinda, Hibberd Tim J, Sharma Harman, Grundy Luke, Brierley Stuart M, Harrington Andrea M, Beckett Elizabeth A, Brookes Simon J, Zagorodnyuk Vladimir P
College of Medicine and Public Health, Centre for Neuroscience, School of Medicine, Flinders University of South Australia, Adelaide, South Australia, Australia.
Centre for Nutrition and Gastrointestinal Diseases, Discipline of Medicine, University of Adelaide, South Australian Health and Medical Research Institute (SAHMRI), North Terrace, Adelaide, South Australia, Australia.
J Comp Neurol. 2018 Mar 1;526(4):707-720. doi: 10.1002/cne.24362. Epub 2017 Dec 15.
Spinal afferent neurons are responsible for the transduction and transmission of noxious (painful) stimuli and innocuous stimuli that do not reach conscious sensations from visceral organs to the central nervous system. Although the location of the nerve cell bodies of spinal afferents is well known to reside in dorsal root ganglia (DRG), the morphology and location of peripheral nerve endings of spinal afferents that transduce sensory stimuli into action potentials is poorly understood. The individual nerve endings of spinal afferents that innervate the urinary bladder have never been unequivocally identified in any species. We used an anterograde tracing technique developed in our laboratory to selectively label only spinal afferents. Mice were anesthetized and unilateral injections of dextran-amine made into lumbosacral DRGs (L5-S2). Seven to nine days postsurgery, mice were euthanized, the urinary bladder removed, then fresh-fixed and stained for immunoreactivity to calcitonin-gene-related-peptide (CGRP). Four distinct morphological types of spinal afferent ending in the bladder were identified. Three types existed in the detrusor muscle and one major type in the sub-urothelium and urothelium. Most nerve endings were located in detrusor muscle where the three types could be identified as having: "branching", "simple", or "complex" morphology. The majority of spinal afferent nerve endings were CGRP-immunoreactive. Single spinal afferent axons bifurcated many times upon entering the bladder and developed varicosities along their axon terminal endings. We present the first morphological identification of spinal afferent nerve endings in the mammalian urinary bladder.
脊髓传入神经元负责将有害(疼痛)刺激以及来自内脏器官但未达到有意识感觉的无害刺激转导并传递至中枢神经系统。尽管脊髓传入神经的神经细胞体位于背根神经节(DRG)这一位置已为人熟知,但对于将感觉刺激转化为动作电位的脊髓传入神经外周神经末梢的形态和位置却知之甚少。在任何物种中,支配膀胱的脊髓传入神经的单个神经末梢都从未被明确识别出来。我们使用了在我们实验室开发的顺行追踪技术来仅选择性地标记脊髓传入神经。将小鼠麻醉后,向腰骶部背根神经节(L5 - S2)单侧注射葡聚糖胺。术后7至9天,对小鼠实施安乐死,取出膀胱,然后新鲜固定并进行降钙素基因相关肽(CGRP)免疫反应性染色。在膀胱中识别出了四种不同形态类型的脊髓传入神经末梢。三种类型存在于逼尿肌中,一种主要类型存在于膀胱上皮下和膀胱上皮中。大多数神经末梢位于逼尿肌中,在那里这三种类型可被识别为具有“分支状”、“简单型”或“复杂型”形态。大多数脊髓传入神经末梢具有CGRP免疫反应性。单个脊髓传入神经轴突进入膀胱后多次分叉,并在其轴突末端形成膨体。我们首次对哺乳动物膀胱中的脊髓传入神经末梢进行了形态学鉴定。