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Characteristics of sensory DRG neurons innervating the wrist joint in rats.

机译:触觉大鼠腕关节的感觉性DRG神经元的特征。

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BACKGROUND: Wrist pain can be the result of trauma, or inflammatory processes such as arthritis or synovitis. There is evidence that sensory nerve fibers are present in the wrist joints of animals and humans; however, the sensory innervation pattern of the wrist, as well as the types of nerves innervating it, have not been clarified. The purpose of this study was to characterize the types of sensory dorsal root ganglion (DRG) neurons innervating the wrist joint in the rat. METHODS: In this study, retrograde neurotransport was combined with lectin affinity histochemistry and immunohistochemistry to characterize DRG neurons innervating the wrist joint in rats. We used 3 markers: calcitonin gene-related peptide (CGRP) as a marker of small, peptide-containing neurons associated with inflammatory pain; the glycoprotein binding the isolectin from Griffonia simplicifolia (IB4) for small, non-peptide-containing neurons related to transmission of pain following nerve injury; and neurofilament 200 (NF200) for small and large myelinated fibers. IB4-binding and CGRP-containing neurons are typically involved in pain sensation, whereas NF200 is associated with pain and proprioception. RESULTS: Neurons innervating the wrist joints, retrogradely labeled with fluoro-gold (FG), were distributed throughout DRGs from C6 to T1. Of all of the FG labeled neurons, the percentage of NF200 immunoreactive (IR) neurons and CGRP-IR neurons were 26% and 45%, respectively. The percentage of IB4-binding neurons was 3%, significantly less than the ratio of CGRP-IR neurons to the total FG labeled neurons. CONCLUSION: Under physiological conditions in rats, DRG neurons transmit several types of sensation from the wrist joint including proprioception and pain. Most of the labeled neurons were CGRP-IR peptide containing neurons. It is likely that these neurons are the predominant afferents for inflammatory pain signals from the wrist. Because peptide-containing neurons are associated with inflammatory pain, it is likely that the inflammation in the wrist joint causes wrist joint pain.
机译:背景:腕关节疼痛可能是外伤或诸如关节炎或滑膜炎之类的炎症过程的结果。有证据表明,动物和人类的腕关节中存在感觉神经纤维。然而,手腕的感觉神经支配方式以及支配神经的神经类型尚未阐明。这项研究的目的是表征支配大鼠腕关节的感觉背根神经节(DRG)神经元的类型。方法:在这项研究中,逆行神经转运与凝集素亲和组织化学和免疫组织化学相结合,以表征神经支配腕关节的DRG神经元。我们使用了3种标记物:降钙素基因相关肽(CGRP)作为与炎症性疼痛相关的含有肽的小神经元的标记物;糖蛋白结合了辛普林(IBR)的异凝集素,用于与神经损伤后疼痛传递有关的小的,不含肽的神经元;和神经丝200(NF200),分别用于大,小的髓鞘纤维。 IB4结合和含CGRP的神经元通常与疼痛感有关,而NF200与疼痛和本体感受有关。结果:神经节支配腕关节,以氟金(FG)逆行标记,分布在从C6到T1的整个DRG中。在所有FG标记的神经元中,NF200免疫反应(IR)神经元和CGRP-IR神经元的百分比分别为26%和45%。结合IB4的神经元的百分比为3%,大大低于CGRP-IR神经元与FG标记的神经元总数的比率。结论:在大鼠的生理条件下,DRG神经元从腕关节传递包括本体感受和疼痛在内的几种感觉。大部分标记的神经元是含有CGRP-1R肽的神经元。这些神经元很可能是腕部发炎性疼痛信号的主要传入者。由于含肽的神经元与炎症性疼痛相关,因此腕关节中的炎症可能会导致腕关节疼痛。

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