Department of Pathology, Faculty of Veterinary Medicine, Alexandria University, Edfina 22758, Egypt.
Department of Pathology, Faculty of Veterinary Medicine, Alexandria University, Edfina 22758, Egypt.
Life Sci. 2019 Oct 1;234:116786. doi: 10.1016/j.lfs.2019.116786. Epub 2019 Aug 22.
Extensive degeneration of articular cartilage (AC) is a primary event in the pathogenesis of osteoarthritis (OA) and other types of joint and bone inflammation. OA results in the loss of joint function, usually accompanied by severe pain, and are the most common type of arthritis, affecting more than 10% of adults. The characteristic signs of OA are progressive cartilage destruction and, eventually, complete loss of chondrocytes. A key enzyme responsible for these degenerative changes in cartilage is matrix metalloproteinase-13 (MMP-13), which is thought to be a major contributor to the degenerative process occurring during OA pathogenesis. The aim of the present review is to shed light on the general role of MMPs, with special emphasis on MMP-13, in the induction of OA and the general basis of OA treatment. The pathogenic mechanism of this highly prevalent disease is not clear, and no effective disease-modifying treatment is currently available. Any updated information about OA treatment in human patients will also benefit companion animals such as horses and dogs, which also suffer from OA. Selective inhibition of MMP-13 seems to be an attractive therapeutic strategy.
关节软骨(AC)的广泛退化是骨关节炎(OA)和其他类型关节和骨骼炎症发病机制中的主要事件。OA 会导致关节功能丧失,通常伴有严重疼痛,是最常见的关节炎类型,影响超过 10%的成年人。OA 的特征性标志是进行性软骨破坏,最终导致软骨细胞完全丧失。负责软骨这些退行性变化的关键酶是基质金属蛋白酶-13(MMP-13),它被认为是 OA 发病过程中退行性过程的主要贡献者。本综述的目的是阐明 MMPs 的一般作用,特别强调 MMP-13 在诱导 OA 中的作用,以及 OA 治疗的一般基础。这种高度流行疾病的发病机制尚不清楚,目前尚无有效的疾病修正治疗方法。有关人类患者 OA 治疗的任何最新信息也将使马和狗等伴侣动物受益,这些动物也患有 OA。选择性抑制 MMP-13 似乎是一种有吸引力的治疗策略。
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