Effects of fasudil on glial cell activation induced by tooth movement.

IF 4.8 2区 医学 Q1 Dentistry Progress in Orthodontics Pub Date : 2024-07-22 DOI:10.1186/s40510-024-00518-2
Wenyuanfeng Chen, Yuan Qu, Yining Liu, Guorui Zhang, Hasan M Sharhan, Xinzhu Zhang, Kunwu Zhang, Baocheng Cao
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Abstract

Background: Orthodontic pain affects the physical and mental health of patients. The spinal trigeminal subnucleus caudalis (SPVC) contributes to the transmission of pain information and serves as a relay station for integrating orofacial damage information. Recently, glial cells have been found to be crucial for both acute and maintenance phases of pain. It has also been demonstrated that rho kinase (ROCK) inhibitors can manage different pain models by inhibiting glial cell activation. Here, we hypothesized that orthodontic pain is related to glial cells in the SPVC, and Fasudil, a representative rho/rock kinase inhibitor, can relieve orthodontic pain by regulating the function of glial cells and the related inflammatory factors. In this study, we constructed a rat model of tooth movement pain and used immunofluorescence staining to evaluate the activation of microglia and astrocytes. Quantitative real-time PCR was used to detect the release of related cytokines and the expression of pain-related genes in the SPVC. Simultaneously, we investigated the effect of Fasudil on the aforementioned indicators.

Results: In the SPVC, the expression of c-Fos peaked on day 1 along with the expression of OX42 (related to microglial activation), CD16 (a pro-inflammatory factor), and CD206 (an anti-inflammatory factor) on day 3 after tooth movement, followed by a gradual decrease. GFAP-staining showed that the number of activated astrocytes was the highest on day 5 and that cell morphology became complex. After Fasudil treatment, the expression of these proteins showed a downward trend. The mRNA levels of pro-inflammatory factors (IL-1β and TNF-α) peaked on day 3, and the mRNA expression of the anti-inflammatory factor TGF-β was the lowest 3 days after tooth movement. Fasudil inhibited the mRNA expression of pain-related genes encoding CSF-1, t-PA, CTSS, and BDNF.

Conclusion: This study shows that tooth movement can cause the activation of glial cells in SPVC, and ROCK inhibitor Fasudil can inhibit the activation of glial cells and reduce the expression of the related inflammatory factors. This study presents for the first time the potential application of Fasudil in othodontic pain.

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法舒地尔对牙齿移动引起的神经胶质细胞活化的影响
背景:正畸疼痛影响患者的身心健康。脊髓三叉神经尾下核(SPVC)有助于疼痛信息的传递,是整合口面部损伤信息的中继站。最近,人们发现神经胶质细胞对疼痛的急性期和维持期都至关重要。研究还表明,Rho 激酶(ROCK)抑制剂可以通过抑制神经胶质细胞的活化来控制不同的疼痛模型。在此,我们假设正畸疼痛与 SPVC 中的神经胶质细胞有关,而具有代表性的 rho/rock 激酶抑制剂 Fasudil 可以通过调节神经胶质细胞的功能和相关炎症因子来缓解正畸疼痛。在本研究中,我们构建了大鼠牙齿移动疼痛模型,并使用免疫荧光染色法评估了小胶质细胞和星形胶质细胞的活化情况。利用定量实时 PCR 检测相关细胞因子的释放以及 SPVC 中疼痛相关基因的表达。同时,我们还研究了法舒地尔对上述指标的影响:结果:在 SPVC 中,c-Fos 的表达在移牙后第 1 天达到峰值,OX42(与小胶质细胞活化有关)、CD16(促炎因子)和 CD206(抗炎因子)的表达在移牙后第 3 天达到峰值,随后逐渐下降。GFAP 染色显示,活化星形胶质细胞的数量在第 5 天最多,细胞形态变得复杂。法舒地尔治疗后,这些蛋白的表达呈下降趋势。促炎因子(IL-1β和TNF-α)的mRNA水平在移牙后第3天达到峰值,而抗炎因子TGF-β的mRNA表达在移牙后3天最低。法舒地尔抑制了编码CSF-1、t-PA、CTSS和BDNF的疼痛相关基因的mRNA表达:本研究表明,牙齿移动可引起 SPVC 中神经胶质细胞的活化,而 ROCK 抑制剂 Fasudil 可抑制神经胶质细胞的活化并减少相关炎症因子的表达。本研究首次提出了法舒地尔在牙科疼痛中的潜在应用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Progress in Orthodontics
Progress in Orthodontics Dentistry-Orthodontics
CiteScore
7.30
自引率
4.20%
发文量
45
审稿时长
13 weeks
期刊介绍: Progress in Orthodontics is a fully open access, international journal owned by the Italian Society of Orthodontics and published under the brand SpringerOpen. The Society is currently covering all publication costs so there are no article processing charges for authors. It is a premier journal of international scope that fosters orthodontic research, including both basic research and development of innovative clinical techniques, with an emphasis on the following areas: • Mechanisms to improve orthodontics • Clinical studies and control animal studies • Orthodontics and genetics, genomics • Temporomandibular joint (TMJ) control clinical trials • Efficacy of orthodontic appliances and animal models • Systematic reviews and meta analyses • Mechanisms to speed orthodontic treatment Progress in Orthodontics will consider for publication only meritorious and original contributions. These may be: • Original articles reporting the findings of clinical trials, clinically relevant basic scientific investigations, or novel therapeutic or diagnostic systems • Review articles on current topics • Articles on novel techniques and clinical tools • Articles of contemporary interest
期刊最新文献
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