Centro de Investigaciones Odontologicas, Pontificia Universidad Javeriana, Bogotá, Colombia.
Endodontics Department, Universidad Cooperativa de Colombia, Pasto, Colombia.
BMC Oral Health. 2021 Mar 23;21(1):152. doi: 10.1186/s12903-021-01519-x.
The aim of this study was to measure the dental pulp inflammatory response through neuropeptides (SP and CGRP) as a response to occlusal trauma, orthodontic movements and a combination of both, as well as the angiogenic defense mechanism through VEGF expression, which could be the initial step to mineralized tissue formation.
Forty human dental pulp samples were collected from healthy first premolars with extraction indicated due to orthodontic reasons from a sample of 20 patients. Patients were divided into four groups with 10 premolars each (1 mandibular and 1 maxillary premolar from each patient): healthy pulp control group, occlusal trauma group, moderate orthodontic forces group; and occlusal trauma plus moderate orthodontic forces group. Stimuli were applied for 24 h before tooth extraction in all experimental groups. All samples were processed, and SP, CGRP, and VEGF were measured by radioimmunoassay. The Kruskal-Wallis test was performed to assess significant differences among groups and Mann-Whitney's U post hoc pairwise comparisons were also performed.
The highest increase in SP, CGRP, and VEGF expressions was found in the occlusal trauma plus orthodontic forces group, followed by the moderate orthodontic forces, the occlusal trauma and the control groups, with statistically significant differences between all groups for each of the 3 peptides analyzed (Kruskal-Wallis p < 0.001). All possible pairwise post-hoc comparisons were also significant for each peptide analyzed (Mann-Whitney's U p < 0.001).
SP, CGRP, and VEGF expressions significantly increase in human dental pulps when stimulated by occlusal trauma combined with moderate orthodontic forces, as compared with these two stimuli applied independently. Name of the registry: Importance of Neurogenic Inflammation in the Angiogenic Response of the Dental Pulp as a Defensive Response.
NCT03804034. Date of registration: 01/15/2019 Retrospectively registered. URL of trial registry record: https://clinicaltrials.gov/ct2/show/NCT03804034?term=NCT03804034&draw=2&rank=1 .
本研究旨在通过神经肽(SP 和 CGRP)测量牙髓的炎症反应,作为对咬合创伤、正畸运动以及两者结合的反应,以及通过 VEGF 表达的血管生成防御机制,这可能是矿化组织形成的初始步骤。
从 20 名患者的样本中,从因正畸原因而拔除的健康第一前磨牙中收集了 40 个人类牙髓样本。患者分为 4 组,每组 10 颗前磨牙(每组 1 颗下颌前磨牙和 1 颗上颌前磨牙):健康牙髓对照组、咬合创伤组、中度正畸力组;以及咬合创伤加中度正畸力组。所有实验组均在拔牙前 24 小时给予刺激。所有样本均经过处理,通过放射免疫法测量 SP、CGRP 和 VEGF。采用 Kruskal-Wallis 检验评估组间差异,采用 Mann-Whitney U 检验进行事后两两比较。
SP、CGRP 和 VEGF 表达的最高增加发生在咬合创伤加正畸力组,其次是中度正畸力组、咬合创伤组和对照组,对于分析的 3 种肽中的每一种,组间均有统计学差异(Kruskal-Wallis p<0.001)。对于分析的每种肽,所有可能的事后两两比较均有统计学意义(Mann-Whitney U p<0.001)。
与这两种刺激单独作用相比,当牙髓受到咬合创伤和中度正畸力联合刺激时,SP、CGRP 和 VEGF 的表达明显增加。
神经源性炎症对牙髓血管生成反应的重要性作为防御反应。
NCT03804034。注册日期:2019 年 1 月 15 日,回顾性注册。试验注册表网址:https://clinicaltrials.gov/ct2/show/NCT03804034?term=NCT03804034&draw=2&rank=1。