Xie Xinru, Chao Rui, Mao Yi, Wan Tianhao, Wang Yexin, Zhu Yan, Xu Weifeng, Chen Xuzhuo, Wang Yong, Ma Zhigui, Zhang Shanyong
Department of Oral Surgery, Shanghai Ninth People's Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, 200011, China.
College of Stomatology, Shanghai Jiao Tong University, Shanghai, 200011, China.
Sci Rep. 2025 Jan 10;15(1):1646. doi: 10.1038/s41598-024-81306-0.
Temporomandibular joint osteoarthritis (TMJOA) is a common degenerative disease that causes chronic pain and joint dysfunction. However, the current understanding of TMJOA pathogenesis is limited and necessitates further research. Animal models are crucial for investigating TMJOA due to the scarcity of clinical samples. Class II malocclusion is an occlusal type highly associated with TMJOA, but it currently lacks appropriate animal models for simulating this malocclusion in research. Therefore, this study develops a new malocclusion model using a unilateral anterior large overjet (UALO) dental device to cause Class II malocclusion characteristics and TMJOA-like pathological alterations in rats. By inducing a posteriorly positioned condyle, the UALO device effectively results in cartilage degradation, subchondral bone loss, condylar volume reduction, and mandibular retrusion. Furthermore, RNA sequencing of condylar cartilages revealed that the oxidative stress of chondrocytes was elevated under the UALO-triggered abnormal mechanical stress. Disruption of antioxidant systems and mitochondrial dysfunction are involved in cartilage degeneration. The current study provides a novel and reliable rat model suitable for TMJOA research and offers insights into the disease's potential mechanistic pathways and molecular targets, contributing to a deeper understanding of TMJOA.
颞下颌关节骨关节炎(TMJOA)是一种常见的退行性疾病,可导致慢性疼痛和关节功能障碍。然而,目前对TMJOA发病机制的了解有限,需要进一步研究。由于临床样本稀缺,动物模型对于研究TMJOA至关重要。II类错牙合是一种与TMJOA高度相关的咬合类型,但目前在研究中缺乏用于模拟这种错牙合的合适动物模型。因此,本研究使用单侧前牙大覆盖(UALO)牙科装置开发了一种新的错牙合模型,以在大鼠中引起II类错牙合特征和TMJOA样病理改变。通过诱导髁突后移,UALO装置有效地导致软骨降解、软骨下骨丢失、髁突体积减小和下颌后缩。此外,髁突软骨的RNA测序显示,在UALO引发的异常机械应力下,软骨细胞的氧化应激升高。抗氧化系统的破坏和线粒体功能障碍与软骨退变有关。本研究提供了一种适用于TMJOA研究的新型可靠大鼠模型,并为该疾病的潜在机制途径和分子靶点提供了见解,有助于更深入地了解TMJOA。