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牙髓炎症后异位持续性牙髓痛的发生机制。

Mechanisms underlying ectopic persistent tooth-pulp pain following pulpal inflammation.

机构信息

Department of Endodontics, Nihon University School of Dentistry, Tokyo, Japan.

出版信息

PLoS One. 2013;8(1):e52840. doi: 10.1371/journal.pone.0052840. Epub 2013 Jan 16.

Abstract

In order to clarify the peripheral mechanisms of ectopic persistent pain in a tooth pulp following pulpal inflammation of an adjacent tooth, masseter muscle activity, phosphorylated extracellular signal-regulated protein kinase (pERK) and TRPV1 immunohistochemistries and satellite cell activation using glial fibrillary acidic protein (GFAP) immunohistochemistry in the trigeminal ganglion (TG) were studied in the rats with molar tooth-pulp inflammation. And, Fluorogold (FG) and DiI were also used in a neuronal tracing study to analyze if some TG neurons innervate more than one tooth pulp. Complete Freund's adjuvant (CFA) or saline was applied into the upper first molar tooth pulp (M1) in pentobarbital-anesthetized rats, and capsaicin was applied into the upper second molar tooth pulp (M2) on day 3 after the CFA or saline application. Mean EMG activity elicited in the masseter muscle by capsaicin application to M2 was significantly larger in M1 CFA-applied rats compared with M1 vehicle-applied rats. The mean number of pERK-immunoreactive (IR) TG cells was significantly larger in M1 CFA-applied rats compared with M1 vehicle-applied rats. Application of the satellite cell inhibitor fluorocitrate (FC) into TG caused a significant depression of capsaicin-induced masseter muscle activity and a significant reduction of satellite cell activation. The number of TRPV1-IR TG cells innervating M2 was significantly larger in M1 CFA-applied rats compared with M1 vehicle-applied rats, and that was decreased following FC injection into TG. Furthermore, 6% of TG neurons innervating M1 and/or M2 innervated both M1 and M2. These findings suggest that satellite cell activation following tooth pulp inflammation and innervation of multiple tooth pulps by single TG neurons may be involved in the enhancement of the activity of TG neurons innervating adjacent non-inflamed teeth that also show enhancement of TRPV1 expression in TG neurons, resulting in the ectopic persistent tooth-pulp pain following pulpal inflammation of adjacent teeth.

摘要

为了阐明邻牙牙髓炎症后牙内髓组织异位持续痛的周围机制,研究了牙髓炎症大鼠三叉神经节(TG)中咀嚼肌活动、磷酸化细胞外信号调节激酶(pERK)和 TRPV1 免疫组织化学以及胶质纤维酸性蛋白(GFAP)免疫组织化学标记的卫星细胞激活情况。此外,还使用荧光金(FG)和 DiI 进行神经元示踪研究,以分析是否有一些 TG 神经元支配不止一个牙髓。在戊巴比妥麻醉大鼠中,将完全弗氏佐剂(CFA)或生理盐水应用于上颌第一磨牙牙髓(M1),并在 CFA 或生理盐水应用后第 3 天将辣椒素应用于上颌第二磨牙牙髓(M2)。与 M1 载体应用大鼠相比,M1 CFA 应用大鼠中咀嚼肌因辣椒素应用而引起的平均 EMG 活动明显更大。与 M1 载体应用大鼠相比,M1 CFA 应用大鼠中 pERK 免疫反应性(IR)TG 细胞的平均数量明显更大。将卫星细胞抑制剂氟柠檬酸(FC)应用于 TG 会导致咀嚼肌活动的显著抑制,以及卫星细胞激活的显著减少。与 M1 载体应用大鼠相比,M1 CFA 应用大鼠中支配 M2 的 TRPV1-IR TG 细胞数量明显更大,并且在将 FC 注射到 TG 后减少。此外,6%的支配 M1 和/或 M2 的 TG 神经元支配 M1 和 M2 两者。这些发现表明,牙髓炎症后的卫星细胞激活以及单个 TG 神经元支配多个牙髓可能参与增强支配相邻未发炎牙齿的 TG 神经元的活动,这些神经元在 TG 神经元中也表现出 TRPV1 表达增强,导致邻牙牙髓炎症后出现异位持续牙髓痛。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b1d/3547043/c6e373af48a9/pone.0052840.g001.jpg

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