Department of Nursing, Al-Maarif University College, Ramadi, Iraq.
Department of Biology, College of Education for Pure Sciences, Wasit University, Kut, Iraq.
J Membr Biol. 2023 Jun;256(3):223-228. doi: 10.1007/s00232-023-00282-0. Epub 2023 Mar 15.
Osteoarthritis (OA) is the most common type of arthritis. Its high prevalence, especially in the elderly, and its negative impact on physical function make it a leading cause of disability in the elderly. Joint pain as well joint stiffness are the common classic signs of OA. Chondrocyte death together with loss of articular cartilage integrity are the main pathologic changes in OA. Non-steroidal anti-inflammatory drugs (NSAIDs) and glucocorticoids are commonly used for the management of OA; still, their effectiveness is limited, and no therapeutic strategy is able to fully stop OA progression. Ferroptosis is a kind of cell death, distinct from apoptosis and necroptosis, caused by iron-dependent peroxidation of membrane phospholipids that terminates cell life by disintegrating all plasma membranes. It has been suggested that ferroptosis has a critical role in decreased viability of chondrocytes in OA, and here, we review recent findings regarding the pathologic pathways that lead to chondrocyte ferroptosis, and discuss the possible therapeutic utility of ferroptosis inhibition in OA.
骨关节炎(OA)是最常见的关节炎类型。其高发病率,特别是在老年人中,以及对身体功能的负面影响,使其成为老年人残疾的主要原因。关节疼痛以及关节僵硬是 OA 的常见经典症状。软骨细胞死亡以及关节软骨完整性丧失是 OA 的主要病理变化。非甾体抗炎药(NSAIDs)和糖皮质激素常用于 OA 的治疗;然而,它们的疗效有限,没有治疗策略能够完全阻止 OA 的进展。铁死亡是一种细胞死亡形式,与细胞凋亡和坏死性凋亡不同,它是由膜磷脂的铁依赖性过氧化引起的,通过破坏所有质膜来终止细胞生命。有研究表明,铁死亡在 OA 中软骨细胞活力下降中起关键作用,在此,我们综述了导致软骨细胞铁死亡的病理途径的最新发现,并讨论了铁死亡抑制在 OA 中的可能治疗应用。