Chung Man-Kyo, Wang Sheng, Alshanqiti Ishraq, Hu Jiaxin, Ro Jin Y
Department of Neural and Pain Sciences, School of Dentistry, Program in Neuroscience, Center to Advance Chronic Pain Research, University of Maryland Baltimore, Baltimore, MD, United States.
Front Pain Res (Lausanne). 2023 Feb 9;4:1038808. doi: 10.3389/fpain.2023.1038808. eCollection 2023.
Temporomandibular disorders (TMD) represent a group of musculoskeletal conditions involving the temporomandibular joints (TMJ), the masticatory muscles and associated structures. Painful TMD are highly prevalent and conditions afflict 4% of US adults annually. TMD include heterogenous musculoskeletal pain conditions, such as myalgia, arthralgia, and myofascial pain. A subpopulations of TMD patients show structural changes in TMJ, including disc displacement or degenerative joint diseases (DJD). DJD is a slowly progressing, degenerative disease of the TMJ characterized by cartilage degradation and subchondral bone remodeling. Patients with DJD often develop pain (TMJ osteoarthritis; TMJ OA), but do not always have pain (TMJ osteoarthrosis). Therefore, pain symptoms are not always associated with altered TMJ structures, which suggests that a causal relationship between TMJ degeneration and pain is unclear. Multiple animal models have been developed for determining altered joint structure and pain phenotypes in response to various TMJ injuries. Rodent models of TMJOA and pain include injections to induce inflammation or cartilage destruction, sustained opening of the oral cavity, surgical resection of the articular disc, transgenic approaches to knockout or overexpress key genes, and an integrative approach with superimposed emotional stress or comorbidities. In rodents, TMJ pain and degeneration occur during partially overlapping time periods in these models, which suggests that common biological factors may mediate TMJ pain and degeneration over different time courses. While substances such as intra-articular pro-inflammatory cytokines commonly cause pain and joint degeneration, it remains unclear whether pain or nociceptive activities are causally associated with structural degeneration of TMJ and whether structural degeneration of TMJ is necessary for producing persistent pain. A thorough understanding of the determining factors of pain-structure relationships of TMJ during the onset, progression, and chronification by adopting novel approaches and models should improve the ability to simultaneously treat TMJ pain and TMJ degeneration.
颞下颌关节紊乱病(TMD)是一组涉及颞下颌关节(TMJ)、咀嚼肌及相关结构的肌肉骨骼疾病。疼痛性TMD非常普遍,每年影响4%的美国成年人。TMD包括多种肌肉骨骼疼痛疾病,如肌痛、关节痛和肌筋膜疼痛。一部分TMD患者的TMJ会出现结构变化,包括盘状移位或退行性关节疾病(DJD)。DJD是一种TMJ的缓慢进展性退行性疾病,其特征是软骨降解和软骨下骨重塑。DJD患者常出现疼痛(TMJ骨关节炎;TMJ OA),但并非总是疼痛(TMJ骨关节病)。因此,疼痛症状并不总是与TMJ结构改变相关,这表明TMJ退变与疼痛之间的因果关系尚不清楚。已经开发了多种动物模型来确定各种TMJ损伤后关节结构改变和疼痛表型。TMJOA和疼痛的啮齿动物模型包括注射诱导炎症或软骨破坏、持续张口、关节盘手术切除、基因敲除或过表达关键基因的转基因方法,以及叠加情绪应激或合并症的综合方法。在啮齿动物中,这些模型中TMJ疼痛和退变在部分重叠的时间段内发生,这表明常见的生物学因素可能在不同的时间进程中介导TMJ疼痛和退变。虽然关节内促炎细胞因子等物质通常会导致疼痛和关节退变,但疼痛或伤害性活动是否与TMJ结构退变存在因果关系,以及TMJ结构退变是否是产生持续性疼痛所必需的,仍不清楚。通过采用新方法和模型,深入了解TMJ在发病、进展和慢性化过程中疼痛-结构关系的决定因素,应能提高同时治疗TMJ疼痛和TMJ退变的能力。