Department of Orthodontics, School of Dental Medicine, University of Belgrade, Belgrade, Serbia.
Department of Pharmacology in Dentistry, School of Dental Medicine, University of Belgrade, Belgrade, Serbia.
Arch Oral Biol. 2020 Feb;110:104599. doi: 10.1016/j.archoralbio.2019.104599. Epub 2019 Nov 9.
We aimed to investigate alteration in cellular signaling mediated by vascular endothelial growth factor (VEGF) and parameters of oxidative stress/nitric oxide generation, superoxide dismutase (SOD) and neuronal nitric oxide synthase (nNOS), underlying altered functional mechanical loading of TMJ (temporomandibular joint) during lateral mandibular deviation.
Thirty-eight 5-week-old male Wistar rats were divided into experimental group, which received acrylic resin appliance that shifted mandible to the left during closure, and control group. Computed tomography and histomorphometry were used for condyle analyses, while samples of condyle, synovial membrane and m. masseter were analyzed with enzyme-linked immunosorbent assay and spectrophotometry to determine VEGF and nNOS protein concentrations, and SOD activity.
Experimental group of rats developed smaller and asymmetrical mandibles. Less of new bone and cartilage formation and larger bone marrow cavities area were found in the experimental group. Higher VEGF expression in condyle and m. masseter as well as higher nNOS expression in m. masseter and synovial membrane were found in the experimental compared to the control group. Alteration of SOD activity was found in m. masseter and synovial membrane in the experimental group.
Lateral mandibular deviation induces mandibular and condylar morphological changes as well as significant cellular signaling alterations in condyle, synovial membrane and masticatory muscle. Cellular VEGF protein overexpression and oxidative stress/nitric oxide disbalance could be the mechanisms underlying unbalanced functional TMJ loading due to mandibular deviation.
我们旨在研究血管内皮生长因子 (VEGF) 介导的细胞信号转导改变,以及氧化应激/一氧化氮生成参数,超氧化物歧化酶 (SOD) 和神经元型一氧化氮合酶 (nNOS),在 TMJ(颞下颌关节)在侧向下颌偏斜期间改变功能机械加载的基础上。
38 只 5 周龄雄性 Wistar 大鼠分为实验组和对照组。实验组在闭合时接受将下颌向左移位的丙烯酸树脂器具,对照组。使用计算机断层扫描和组织形态计量学对髁突进行分析,同时使用酶联免疫吸附测定法和分光光度法分析髁突、滑膜和咀嚼肌样本,以确定 VEGF 和 nNOS 蛋白浓度以及 SOD 活性。
实验组大鼠发育出较小和不对称的下颌骨。实验组发现新骨和软骨形成较少,骨髓腔面积较大。实验组髁突和咀嚼肌中的 VEGF 表达以及咀嚼肌和滑膜中的 nNOS 表达均高于对照组。实验组咀嚼肌和滑膜中的 SOD 活性发生改变。
侧向下颌偏斜会导致下颌骨和髁突形态发生变化,以及髁突、滑膜和咀嚼肌中明显的细胞信号转导改变。细胞 VEGF 蛋白过表达和氧化应激/一氧化氮失衡可能是由于下颌偏斜导致 TMJ 功能加载失衡的机制。