Magari K, Miyata S, Ohkubo Y, Mutoh S
Medicinal Biology Research Laboratories, Fujisawa Pharmaceutical Co., Ltd., 2-1-6, Kashima, 532-8514 Yodogawa-ku, Osaka, Japan.
Inflamm Res. 2004 Sep;53(9):469-74. doi: 10.1007/s00011-004-1284-y.
To characterize rat collagen-induced arthritis (CIA) on the basis of levels of inflammatory cytokines, tumor necrosis factor (TNF)-alpha, interleukin (IL)-1beta and IL-6 in paw tissues, and further investigate the effect of FK506 (tacrolimus), a potent inhibitor of T cell activation, on cytokine levels.
CIA was induced in female Lewis rats. The volume of hindpaws was measured before and after collagen immunization. TNF-alpha, IL-1beta and IL-6 levels in paw tissue extracts were determined by ELISA. Proteoglycan contents of cartilage in femoral heads was measured as an indication of cartilage destruction. To assess the effect of FK506 on inflammatory cytokine levels, rats were orally treated with 5 mg/kg of FK506 from days 14-21.
TNF-alpha a level in paw tissues did not significantly change compared to levels found before collagen immunization, throughout development of CIA. In contrast, IL-1beta and IL-6 levels in paw tissues significantly increased between day 14 and day 28 after collagen imuninization, when the arthritis was at a developed stage. Therapeutic treatment with FK506 reduced the elevated level of IL-6, but not IL-1beta, in paw tissue. FK506 treatment was effective in suppressing paw swelling and also recovering the loss of proteoglycan contents in the cartilage.
Levels of IL-1beta and IL-6, but not TNF-alpha , in paw tissue were upregulated in association with the development of arthritis in rat CIA. These results suggest that IL-1beta and IL-6, rather than TNF-alpha , may play important roles at local inflammatory sites in producing joint destruction in rat CIA. FK506 may improve arthritis in established stages of CIA, by reducing the elevated level of IL-6.
基于爪组织中炎性细胞因子、肿瘤坏死因子(TNF)-α、白细胞介素(IL)-1β和IL-6的水平来表征大鼠胶原诱导性关节炎(CIA),并进一步研究T细胞活化的强效抑制剂FK506(他克莫司)对细胞因子水平的影响。
在雌性Lewis大鼠中诱导CIA。在胶原免疫前后测量后爪体积。通过ELISA测定爪组织提取物中TNF-α、IL-1β和IL-6的水平。测量股骨头软骨中蛋白聚糖含量以指示软骨破坏情况。为评估FK506对炎性细胞因子水平的影响,从第14天至第21天对大鼠口服5mg/kg的FK506进行治疗。
在CIA的整个发展过程中,与胶原免疫前的水平相比,爪组织中TNF-α水平没有显著变化。相反,在胶原免疫后第14天至第28天,当关节炎处于发展阶段时,爪组织中IL-1β和IL-6水平显著升高。用FK506进行治疗可降低爪组织中升高的IL-6水平,但不能降低IL-1β水平。FK506治疗可有效抑制爪肿胀,并恢复软骨中蛋白聚糖含量的损失。
在大鼠CIA中,爪组织中IL-1β和IL-6水平而非TNF-α水平随着关节炎的发展而上调。这些结果表明,在大鼠CIA中,IL-1β和IL-6而非TNF-α可能在局部炎症部位导致关节破坏中起重要作用。FK506可能通过降低升高的IL-6水平来改善CIA已确立阶段的关节炎。