Animal models and experimental medicine · 2025
Time- and dose-related pathological changes in knee osteoarthritis rat model induced by monosodium iodoacetate.
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Pu Wei, Liu Qi, Xue Shuyan, Li Siyuan, Nan Nan, Liu Yang, Hao Huiqin
Аннотация
UNLABELLED: Knee osteoarthritis (KOA) is a chronic degenerative disease. Monosodium iodoacetate (MIA) induction is the most commonly used therapeutic effect evaluation and mechanism of action research model; we observed a lack of standardization and uniformity in current model building methods, which led us to conduct this study.
BACKGROUND: The aim was to investigate the time- and dose-related changes in the behavioral and pathological characteristics in the MIA-induced KOA model rat.
METHODS: MIA (40, 50, and 60 mg/mL) was injected into the left joint of male Sprague-Dawley rats. After 2 weeks, the changes in the KOA rat model were observed by behavioral evaluation, imaging-level evaluation, and histological-level evaluation. The changes were also compared after 40-mg/mL MIA injection for 2 and 6 weeks.
RESULTS: MIA-induced bone surface defects, osteophyte hyperplasia around the articular rim, increased subchondral bone density, thinning of the sparse trabecular bone, structural disorder, and local clustering were observed. The degree of injury gradually increased with the increase in MIA concentration. After 6 weeks, subchondral bone density and sparse trabecular bone increased in the KOA model.
CONCLUSIONS: The severity of the model also increased significantly with the changes in dose and time. In dose-dependent experiments, this study revealed that 40 mg/mL was the optimal dose to induce significant pathological changes without causing undue discomfort or death in animals. This dose may induce pathological changes stably and is suitable for long-term observation.
BACKGROUND: The aim was to investigate the time- and dose-related changes in the behavioral and pathological characteristics in the MIA-induced KOA model rat.
METHODS: MIA (40, 50, and 60 mg/mL) was injected into the left joint of male Sprague-Dawley rats. After 2 weeks, the changes in the KOA rat model were observed by behavioral evaluation, imaging-level evaluation, and histological-level evaluation. The changes were also compared after 40-mg/mL MIA injection for 2 and 6 weeks.
RESULTS: MIA-induced bone surface defects, osteophyte hyperplasia around the articular rim, increased subchondral bone density, thinning of the sparse trabecular bone, structural disorder, and local clustering were observed. The degree of injury gradually increased with the increase in MIA concentration. After 6 weeks, subchondral bone density and sparse trabecular bone increased in the KOA model.
CONCLUSIONS: The severity of the model also increased significantly with the changes in dose and time. In dose-dependent experiments, this study revealed that 40 mg/mL was the optimal dose to induce significant pathological changes without causing undue discomfort or death in animals. This dose may induce pathological changes stably and is suitable for long-term observation.