Orhan Cemal, Juturu Vijaya, Sahin Emre, Tuzcu Mehmet, Ozercan Ibrahim Hanifi, Durmus Ali Said, Sahin Nurhan, Sahin Kazim
Department of Animal Nutrition, Faculty of Veterinary Medicine, Firat University, Elazig, Turkey.
Research and Development, Lonza, Morristown, NJ, United States.
Front Vet Sci. 2021 Mar 4;8:617789. doi: 10.3389/fvets.2021.617789. eCollection 2021.
Osteoarthritis (OA) is an age-related joint disease that includes gradual disruption of the articular cartilage and the resulting pain. The present study was designed to test the effects of undenatured type II collagen (UC-II®) on joint inflammation in the monoiodoacetate (MIA) OA model. We also investigated possible mechanisms underlying these effects. Female Wistar rats were divided into three groups: (i) Control; (ii) MIA-induced rats treated with vehicle; (iii) MIA-induced rats treated with UC-II (4 mg/kg BW). OA was induced in rats by intra-articular injection of MIA (1 mg) after seven days of UC-II treatment. UC-II reduced MIA-induced Kellgren-Lawrence scoring (53.3%, < 0.05). The serum levels of inflammatory cytokines [IL-1β (7.8%), IL-6 (18.0%), TNF-α (25.9%), COMP (16.4%), CRP (32.4%)] were reduced in UC-II supplemented group ( < 0.0001). In the articular cartilage, UC-II inhibited the production of PGE2 (19.6%) and the expression of IL-1β, IL-6, TNF-a, COX-2, MCP-1, NF-κB, MMP-3, RANKL ( < 0.001). The COL-1 and OPG levels were increased, and MDA decreased in UC-II supplemented rats ( < 0.001). UC-II could be useful to alleviate joint inflammation and pain in OA joints by reducing the expression of inflammatory mediators.
骨关节炎(OA)是一种与年龄相关的关节疾病,包括关节软骨的逐渐破坏以及由此产生的疼痛。本研究旨在测试未变性II型胶原蛋白(UC-II®)对单碘乙酸盐(MIA)诱导的骨关节炎模型中关节炎症的影响。我们还研究了这些影响背后可能的机制。将雌性Wistar大鼠分为三组:(i)对照组;(ii)用赋形剂处理的MIA诱导大鼠;(iii)用UC-II(4mg/kg体重)处理的MIA诱导大鼠。在UC-II处理7天后,通过关节内注射MIA(1mg)诱导大鼠患骨关节炎。UC-II降低了MIA诱导的凯尔格伦-劳伦斯评分(53.3%,<0.05)。补充UC-II的组中炎症细胞因子[IL-1β(7.8%)、IL-6(18.0%)、TNF-α(25.9%)、COMP(16.4%)、CRP(32.4%)]的血清水平降低(<0.0001)。在关节软骨中,UC-II抑制了PGE2的产生(19.6%)以及IL-1β、IL-6、TNF-α、COX-2、MCP-1、NF-κB、MMP-3、RANKL的表达(<0.001)。补充UC-II的大鼠中COL-1和OPG水平升高,MDA降低(<0.001)。UC-II可能通过降低炎症介质的表达来减轻OA关节的炎症和疼痛。