Li Pengbin, Tang Wenjuan, Wen Haiyan, Zhou Siqi, Cao Hui
Department of Orthopedics, General Hospital of The Yangtze River Shipping, Wuhan Brain Hospital, Wuhan, China.
Department of Radiology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430022, Hubei, China.
Naunyn Schmiedebergs Arch Pharmacol. 2025 Jan 9. doi: 10.1007/s00210-024-03776-3.
Osteoarthritis (OA) is a degenerative musculoskeletal disease, featured by the destruction of articular cartilage. Oxidative stress, one of the drivers of the extracellular matrix degradation in cartilage, plays a vital role in OA pathogenesis. Senkyunolide I (SEI) is a natural compound with a prominent anti-oxidative stress property against multiple diseases. However, the protective effect of SEI on OA has not been explored. Here, we aimed to elucidate the effect of SEI on OA in vitro. Our results showed that SEI suppressed the expression of senescence-related markers such as P16 and P21 in IL-1β-induced chondrocytes. Besides, SEI alleviated IL-1β-induced the degradation of extracellular matrix (ECM) by suppressing the matrix proteinase like MMP13 and ATAMDS5 while promoting matrix synthesis regulated biomarkers like COL2A1 and ACAN in chondrocytes. Mechanically, the mitochondrial dysfunction and overproduction of intracellular reactive oxygen species (ROS) in chondrocytes induced by IL-1β were reversed by SEI. Additionally, the ROS inhibitor N-acetylcysteine (NAC) synergistically enhanced the biological effect of SEI in IL-1β-induced chondrocytes. Moreover, it was also found that the expression of Nrf2 and HO-1 was increased by the treatment of SEI in IL-1β-stimulated chondrocytes, while the Nrf2 inhibitor ML385 reversed the protective effect of SEI on OA chondrocytes. In conclusion, SEI could inhibit senescence, the degradation of ECM, and the production of ROS through activating Nrf2/ HO-1 signaling pathway, which provide a novel candidate for OA treatment.
骨关节炎(OA)是一种退行性肌肉骨骼疾病,其特征是关节软骨遭到破坏。氧化应激作为软骨细胞外基质降解的驱动因素之一,在骨关节炎的发病机制中起着至关重要的作用。党参炔苷I(SEI)是一种天然化合物,对多种疾病具有显著的抗氧化应激特性。然而,SEI对骨关节炎的保护作用尚未得到研究。在此,我们旨在阐明SEI在体外对骨关节炎的影响。我们的结果表明,SEI抑制了白细胞介素-1β诱导的软骨细胞中衰老相关标志物如P16和P21的表达。此外,SEI通过抑制基质蛋白酶如MMP13和ADAMTS5,同时促进软骨细胞中基质合成调节生物标志物如COL2A1和ACAN,减轻了白细胞介素-1β诱导的细胞外基质(ECM)降解。从机制上讲,SEI逆转了白细胞介素-1β诱导的软骨细胞中的线粒体功能障碍和细胞内活性氧(ROS)的过量产生。此外,ROS抑制剂N-乙酰半胱氨酸(NAC)协同增强了SEI在白细胞介素-1β诱导的软骨细胞中的生物学效应。此外,还发现SEI处理可增加白细胞介素-1β刺激的软骨细胞中Nrf2和HO-1的表达,而Nrf2抑制剂ML385则逆转了SEI对骨关节炎软骨细胞的保护作用。总之,SEI可通过激活Nrf2/HO-1信号通路抑制衰老、ECM降解和ROS产生,这为骨关节炎治疗提供了一种新的候选药物。