National JALMA Institute for Leprosy & Other Mycobacterial Diseases (ICMR), Agra, India.
Indian Institute of Technology, Kharagpur, India.
Clin Rheumatol. 2018 Aug;37(8):2195-2201. doi: 10.1007/s10067-018-4087-1. Epub 2018 Apr 10.
The duration and dose-dependent side effects of conventional intra-articular corticosteroid treatment in osteoarthritis (OA) like cartilage damage and chondrocyte toxicity warrant the search for alternative therapeutics. Oxaceprol, a recognized oral therapeutic agent for osteoarthritis, is yet to be explored for its intra-articular route of administration confirming better safety profile. In this study, a comparative evaluation of intra-articular oxaceprol and corticosteroid is carried out in osteoarthritis rabbit model. Osteoarthritis was induced by monosodium iodoacetate in rabbits. After randomization into three groups of five animals each: OA with intra-articular injection of saline, OA with intra-articular injection of oxaceprol, and OA with intra-articular injection of corticosteroids, treatment efficacy was analyzed by evaluation of inflammation through knee swelling, pain assessment by wire walking, and hot plate method. Further biopsies were collected for histological characterization. Intra-articular oxaceprol and corticosteroids reduced 20.5 and 24.5% knee swelling respectively within 4 weeks compared to those in control osteoarthritic rabbits. Oxaceprol exhibited analgesic action in visual analogue scoring of wire walking method. Hot plate test further confirmed drastic minimization of pain in oxaceprol intervention. Histological investigation suggested that application of oxaceprol has the abilities to protect articular cartilages from degenerative changes that occur in osteoarthritis. Marked improvement both in bone and cellular matrixes was observed in oxaceprol-treated group while gross lesions were visible and consisted of a well-demarcated area of cartilage erosion in control group. Intra-articular injection of oxaceprol showed remarkable improvement of articular cartilage in chemically induced osteoarthritic rabbits.
在骨关节炎(OA)中,常规关节内皮质类固醇治疗的持续时间和剂量依赖性副作用,如软骨损伤和软骨细胞毒性,这使得人们需要寻找替代疗法。Oxaceprol 是一种公认的治疗 OA 的口服药物,但其关节内给药途径尚未得到探索,以确认其更好的安全性。在这项研究中,我们在 OA 兔模型中对关节内 Oxaceprol 和皮质类固醇进行了比较评估。通过向兔膝关节内注射单碘乙酸钠诱导 OA。将动物随机分为三组,每组 5 只:OA 关节内注射生理盐水、OA 关节内注射 Oxaceprol 和 OA 关节内注射皮质类固醇。通过膝关节肿胀评估炎症、线行走评估疼痛和热板法评估疼痛,分析治疗效果。进一步收集活检组织进行组织学特征分析。与对照组 OA 兔相比,关节内注射 Oxaceprol 和皮质类固醇分别在 4 周内使膝关节肿胀减少了 20.5%和 24.5%。Oxaceprol 在线行走法的视觉模拟评分中表现出镇痛作用。热板试验进一步证实了 Oxaceprol 干预极大地减轻了疼痛。组织学研究表明,Oxaceprol 的应用具有保护关节软骨免受 OA 发生的退行性变化的能力。在 Oxaceprol 治疗组中观察到骨和细胞基质有明显改善,而在对照组中可见明显的病变,包括软骨侵蚀的界限分明的区域。关节内注射 Oxaceprol 可显著改善化学诱导性 OA 兔的关节软骨。