Kim Jeonghyun, Lee Chang-Gun, Hwang Seokjin, Yun Seung-Hee, Uprety Laxmi Prasad, Oh Kang-Il, Singh Shivani, Yoo Jisu, Jeong Hyesoo, Yong Yoonjoong, Yeo Subin, Park Eunkuk, Jeong Seon-Yong
Department of Medical Genetics, Ajou University School of Medicine, Suwon 16499, Republic of Korea.
Department of Biomedical Sciences, Ajou University Graduate School of Medicine, Suwon 16499, Republic of Korea.
Antioxidants (Basel). 2022 Dec 26;12(1):47. doi: 10.3390/antiox12010047.
Osteoarthritis (OA) is the progressive destruction of articular cartilage with severe symptoms, including pain and stiffness. We investigated the anti-osteoarthritic effects of (PV) and Gentiana lutea (GL) extract in primary cultured chondrocytes RAW 264.7 cells in vitro and destabilization of the medial meniscus (DMM)-induced OA mice in vivo. Primary chondrocytes were induced with IL-1β, and RAW 264.7 cells were treated with LPS and co-incubated with either individual extracts of PV and GL or different ratios of PV and GL mixture. For the OA animal model, the medial meniscus (DMM) was destabilized in 9-week-old male C57BL/6 mice. Treatment of individual PV and GL and combination of PV and GL extracts inhibited the mRNA expression level of in chondrocytes and RAW 264.7 cells. The optimized inhibitory effect was attained with a PV and GL combination at an 8:2 ratio (PG) without cytotoxic effects. PG extracts prevented the expression of catabolic factors ( and ) and inflammatory mediator levels (PGE2 and collagenase). In addition, PG decreased subchondral sclerosis and increased BMD in the subchondral region of DMM-induced OA mice with protection of articular cartilage destruction by inhibiting inflammatory processes. This study suggests that PG may be an alternative medicinal herb for treatment of OA.
骨关节炎(OA)是关节软骨的进行性破坏,伴有疼痛和僵硬等严重症状。我们在体外研究了[植物名称未给出,用PV代替](PV)和黄龙胆(GL)提取物对原代培养软骨细胞RAW 264.7细胞的抗骨关节炎作用,以及在体内对内侧半月板不稳定(DMM)诱导的OA小鼠的作用。原代软骨细胞用IL-1β诱导,RAW 264.7细胞用脂多糖处理,并与PV和GL的单独提取物或不同比例的PV和GL混合物共同孵育。对于OA动物模型,在9周龄雄性C57BL/6小鼠中使内侧半月板(DMM)不稳定。PV和GL单独处理以及PV和GL提取物组合抑制了软骨细胞和RAW 264.7细胞中[相关基因未给出,用“ ”代替]的mRNA表达水平。PV和GL以8:2比例组合(PG)达到了最佳抑制效果,且无细胞毒性作用。PG提取物可阻止分解代谢因子([相关因子未给出,用“ ”和“ ”代替])的表达和炎症介质水平(前列腺素E2和胶原酶)。此外,PG可减轻DMM诱导的OA小鼠软骨下硬化,并增加软骨下区域的骨密度,通过抑制炎症过程保护关节软骨破坏。本研究表明,PG可能是治疗OA的一种替代草药。