INSERM, CHU Lille, U1008 - Controlled Drug Delivery Systems and Biomaterials, University of Lille, Lille, France.
INSERM, CHU Lille, Department of Oral and Maxillofacial Surgery, University of Lille, Lille, France.
PLoS One. 2023 Jan 31;18(1):e0281135. doi: 10.1371/journal.pone.0281135. eCollection 2023.
To compare two agents that can induce a rat model of temporomandibular joint osteoarthritis (TMJOA) by chemical induction: monosodium iodoacetate (MIA) and collagenase type 2 (Col-2). We wished to ascertain the best agent for assessing drug-delivery systems (DDSs).
Male Wistar rats underwent intra-articular injection with MIA or Col-2. They were manipulated for 30 days. The head withdrawal threshold (HWT), immunohistological assessment, and positron emission tomography (PET) were used to evaluate the relevance of our models.
For both the MIA and Col-2 groups, pain persisted for 30 days after injection. Change in the HWT showed that Col-2 elicited a strong action initially that decreased progressively. MIA had a constant action upon pain behavior. Histology of TMJ tissue from both groups showed progressive degradation of TMJ components.
MIA and Col-2 induced orofacial pain by their local chemical action on TMJs. However, based on a prolonged and greater sustained effect on the pain threshold, persistent histological changes, and imaging results, MIA appeared to be more suitable for creation of a rat model of TMJOA for the study of DDSs.
通过化学诱导比较两种可诱导颞下颌关节骨关节炎(TMJOA)大鼠模型的试剂:单碘乙酸盐(MIA)和胶原酶 2(Col-2)。我们希望确定评估药物输送系统(DDS)的最佳试剂。
雄性 Wistar 大鼠接受关节内注射 MIA 或 Col-2。对其进行 30 天的操作。使用头部撤回阈值(HWT)、免疫组织化学评估和正电子发射断层扫描(PET)来评估我们模型的相关性。
对于 MIA 和 Col-2 组,注射后疼痛持续 30 天。HWT 的变化表明,Col-2 最初引起强烈作用,然后逐渐减弱。MIA 对疼痛行为有持续作用。两组 TMJ 组织的组织学均显示 TMJ 成分进行性降解。
MIA 和 Col-2 通过对 TMJ 的局部化学作用引起口面疼痛。然而,基于对疼痛阈值的延长和更大持续影响、持续的组织学变化和影像学结果,MIA 似乎更适合用于 TMJOA 大鼠模型的创建,以研究 DDS。