Veterinary world · 2025
Radiological-behavioral disparities in experimental osteoarthritis: Sex-specific progression and therapeutic response in a rat model.
СтатьяНазвание и аннотация: Перевод в очереди
Обработка статьи · этапы, ошибки и управление
Загрузка состояния…
Ошибки и ограничения
История · было → стало
Состояние обновляется каждые 5 секунд, пока блок открыт. Процент показывается только там, где известен объём работы. Пауза останавливает продолжение этапа; текущий запрос к источнику может завершиться.
Silva Armando Reinaldo Marques, Silva Eduardo Rodrigues, Garcês José Renzo Castro, Pereira Gabriel Moreira, Caldas Raysa Lins, de Figueiredo Isaias Moreira, Ferreira Lilah Karen Ribeiro, Pinheiro Davi de Sousa, Martins Nathalya Dos Santos, Dourado Adriana Araújo, de Sousa Eduardo Martins, Cartágenes Maria do Socorro de Sousa, Carvalho Rafael Cardoso
Аннотация
BACKGROUND AND AIM: Osteoarthritis (OA) is a progressive degenerative joint disorder characterized by cartilage loss, subchondral bone remodeling, and chronic pain, and remains a leading cause of disability worldwide. Although radiographic imaging and behavioral testing are widely used in preclinical research, few studies have systematically examined their interdependence. This study aimed to radiologically characterize OA progression in rats induced by monosodium iodoacetate (MIA) and to correlate structural alterations with functional and nociceptive outcomes, while exploring potential sex-specific differences and therapeutic responses to non-steroidal anti-inflammatory drugs (NSAIDs).
MATERIALS AND METHODS: Thirty-six Wistar rats (male and female) were divided into six experimental groups: Healthy controls, OA-induced untreated, and OA-induced meloxicam-treated. Over 28 days, animals underwent serial radiological assessments and validated behavioral tests, including weight-bearing, rotarod, and Von Frey assays. Statistical analyses employed analysis of variance with post hoc testing, ensuring methodological rigor with blinded evaluators and sex-stratified comparisons.
RESULTS: Radiographs revealed classical OA features, joint space narrowing, subchondral bone sclerosis, and osteophyte formation, with progressive severity across timepoints. NSAID-treated males demonstrated significant improvement in motor coordination and nociceptive thresholds on days 7 and 14 (p < 0.001), whereas females exhibited only modest or delayed responses despite more severe radiological deterioration. Importantly, structural joint damage did not consistently align with behavioral impairments, underscoring a dissociation between radiographic severity and clinical-like manifestations.
CONCLUSION: This study provides an integrated evaluation of structural and functional outcomes in experimental OA, highlighting a complex relationship between radiological changes and behavioral impairments. The findings emphasize the necessity of multimodal assessment strategies in preclinical OA models and reveal sex-specific differences in disease progression and therapeutic response. These insights are crucial for refining translational strategies, advocating for sex-conscious approaches and combined structural-functional endpoints in OA research and drug development.
MATERIALS AND METHODS: Thirty-six Wistar rats (male and female) were divided into six experimental groups: Healthy controls, OA-induced untreated, and OA-induced meloxicam-treated. Over 28 days, animals underwent serial radiological assessments and validated behavioral tests, including weight-bearing, rotarod, and Von Frey assays. Statistical analyses employed analysis of variance with post hoc testing, ensuring methodological rigor with blinded evaluators and sex-stratified comparisons.
RESULTS: Radiographs revealed classical OA features, joint space narrowing, subchondral bone sclerosis, and osteophyte formation, with progressive severity across timepoints. NSAID-treated males demonstrated significant improvement in motor coordination and nociceptive thresholds on days 7 and 14 (p < 0.001), whereas females exhibited only modest or delayed responses despite more severe radiological deterioration. Importantly, structural joint damage did not consistently align with behavioral impairments, underscoring a dissociation between radiographic severity and clinical-like manifestations.
CONCLUSION: This study provides an integrated evaluation of structural and functional outcomes in experimental OA, highlighting a complex relationship between radiological changes and behavioral impairments. The findings emphasize the necessity of multimodal assessment strategies in preclinical OA models and reveal sex-specific differences in disease progression and therapeutic response. These insights are crucial for refining translational strategies, advocating for sex-conscious approaches and combined structural-functional endpoints in OA research and drug development.