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炎症关节和相邻皮肤中的交感神经纤维发芽会导致关节炎相关的疼痛行为。

Sympathetic fiber sprouting in inflamed joints and adjacent skin contributes to pain-related behavior in arthritis.

机构信息

Department of Pharmacology and Therapeutics, McGill University, Montreal, Quebec H3G 1Y6, Canada.

出版信息

J Neurosci. 2013 Jun 12;33(24):10066-74. doi: 10.1523/JNEUROSCI.5784-12.2013.

Abstract

Although chronic pain is the most common symptom of arthritis, relatively little is known about the mechanisms driving it. Recently, a sprouting of autonomic sympathetic fibers into the upper dermis of the skin, an area that is normally devoid of them, was found in the skin following chronic inflammation of the rat hindpaw. While this sprouting only occurred when signs of joint and bone damage were present, it remained to be clarified whether it was a consequence of the chronic inflammation of the skin or of the arthritis and whether it also occurred in the joint. In the present study, we used a model of arthritis in which complete Freund's adjuvant (CFA) was injected into the rat ankle joint. At 4 weeks following CFA treatment, there was an increase in sympathetic and peptidergic fiber density in the ankle joint synovium. We also observed a sympathetic, but not peptidergic, fiber sprouting in the skin over the joint, which may be a consequence of the increased levels of mature nerve growth factor levels in skin, as revealed by Western blot analysis. The pharmacological suppression of sympathetic fiber function with systemic guanethidine significantly decreased the pain-related behavior associated with arthritis. Guanethidine completely suppressed the heat hyperalgesia and attenuated mechanical and cold hypersensitivity. These results suggest that transmitters released from the sprouted sympathetic fibers in the synovial membrane and upper dermis contribute to the pain-related behavior associated with arthritis. Blocking the sympathetic fiber sprouting may provide a novel therapeutic approach to alleviate pain in arthritis.

摘要

虽然慢性疼痛是关节炎最常见的症状,但人们对导致这种疼痛的机制知之甚少。最近,人们在大鼠后爪慢性炎症后的皮肤上层真皮中发现了自主交感神经纤维的萌芽,而这个区域通常是没有这些纤维的。虽然这种萌芽仅在出现关节和骨骼损伤迹象时才会发生,但仍需澄清它是皮肤慢性炎症的结果还是关节炎的结果,以及它是否也发生在关节中。在本研究中,我们使用了一种关节炎模型,其中将完全弗氏佐剂 (CFA) 注射到大鼠踝关节中。在 CFA 治疗后 4 周,踝关节滑膜中的交感和肽能纤维密度增加。我们还观察到关节皮肤中出现了交感神经纤维的萌芽,但没有肽能纤维的萌芽,这可能是由于皮肤中成熟神经生长因子水平升高的结果,如 Western blot 分析所示。用全身性胍乙啶抑制交感纤维功能可显著降低与关节炎相关的疼痛相关行为。胍乙啶完全抑制了热痛觉过敏,并减轻了机械和冷感觉过敏。这些结果表明,源自滑膜和上层真皮中萌芽的交感纤维释放的递质可能与关节炎相关的疼痛相关行为有关。阻断交感纤维的萌芽可能为缓解关节炎疼痛提供一种新的治疗方法。

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