College of Chemical and Biological Engineering, Yichun University, Yichun 336000, China.
Department of Immunology and Pathobiology, Hebei University of Chinese Medicine, Shijiazhuang 050200, China.
Biomed Pharmacother. 2018 Oct;106:255-259. doi: 10.1016/j.biopha.2018.06.130. Epub 2018 Jun 28.
Paeoniflorin (PF) has many effects, such as anti-inflammation, immune-regulation, abirritation, and so on. However, the protective mechanisms of PF on rheumatoid arthritis (RA) was not completely known. Thus, we explored deeply the protective mechanisms in a collagen-induced RA (CIA) rat model. CIA was induced in rats by intradermal injection of bovine type II collagen in complete Freund's adjuvant. Later, the CIA rats received oral administration of PF (50 and 100 mg/kg) once a day from the day 21, with the treatment lasting for 14 days. A variety of indicators were measured for evaluation of anti-rheumatism effect, including paw swelling, arthritis scores, and histopathological changes. And the contents of pro-inflammatory cytokines, including tumor necrosis factor alpha (TNF-α), interleukin-1 beta (IL-1β), and interleukin-6 (IL-6) in the serum, as well as p-NF-κB p65 and p-MYPT1 in the joint synovial tissues were detected to explore the possible mechanisms. The results demonstrated that PF treatment significantly ameliorated the symptoms in CIA rats, reduced the levels of pro-inflammatory cytokines and paw swelling, down-regulated the expressions of p-NF-κB p65 and p-MYPT1. The present results revealed that PF could effectively improve collagen-induced RA in rats by inhibiting Rho kinase activation in the joint synovial tissues, in turn down-regulating expression of p-NF-κB p65 and reducing contents of pro-inflammatory cytokines. Moreover, PF may be an effective agent for RA.
芍药苷(PF)具有抗炎、免疫调节、镇痛等多种作用。然而,PF 对类风湿关节炎(RA)的保护机制尚不完全清楚。因此,我们在胶原诱导的 RA(CIA)大鼠模型中深入探讨了其保护机制。通过在完全弗氏佐剂中皮内注射牛 II 型胶原诱导 CIA 大鼠。随后,CIA 大鼠从第 21 天开始每天口服 PF(50 和 100mg/kg),治疗持续 14 天。通过测量多种指标来评估抗风湿作用,包括爪肿胀、关节炎评分和组织病理学变化。并检测血清中促炎细胞因子(包括肿瘤坏死因子-α(TNF-α)、白细胞介素-1β(IL-1β)和白细胞介素-6(IL-6))以及关节滑膜组织中 p-NF-κB p65 和 p-MYPT1 的含量,以探讨可能的机制。结果表明,PF 治疗可显著改善 CIA 大鼠的症状,减轻促炎细胞因子水平和爪肿胀,下调 p-NF-κB p65 和 p-MYPT1 的表达。本研究结果表明,PF 可通过抑制关节滑膜组织中 Rho 激酶的激活,从而下调 p-NF-κB p65 的表达和降低促炎细胞因子的含量,有效改善胶原诱导的 RA。此外,PF 可能是一种有效的 RA 治疗药物。