Applied Pharmacology Research Laboratories, Drug Discovery Research, Astellas Pharma Inc., Tsukuba, Ibaraki, Japan.
Biol Pharm Bull. 2011;34(12):1823-7. doi: 10.1248/bpb.34.1823.
We investigated the effect of tacrolimus, a calcineurin inhibitor, on dextran sulfate sodium (DSS)-induced colitis. After inducing colitis in C57BL/6 mice by administering DSS solution as drinking water for 7 d, the animals were treated with tacrolimus. Severity of colonic inflammation was evaluated based on colon weight per unit length. Levels of cytokines (interferon (IFN)-γ, interleukin (IL)-1β, IL-2, IL-4, IL-5, IL-6, IL-12, and tumor necrosis factor (TNF)-α) released from isolated inflamed colons of mice treated with tacrolimus or vehicle were also measured. Treatment with tacrolimus for 14 d reduced the colon weight per unit length and suppressed the release of IFN-γ and IL-1β, but not other cytokines, in inflamed colons of colitic mice compared with vehicle-treated mice. A positive correlation was noted between colon weight per unit length and released level of IFN-γ or IL-1β. The release of IFN-γ and IL-1β was also suppressed after single dosing with tacrolimus to colitic mice. Taken together, these results suggested that tacrolimus ameliorated DSS-induced colitis by suppressing release of IFN-γ and IL-1β from inflamed colon.
我们研究了钙调神经磷酸酶抑制剂他克莫司对葡聚糖硫酸钠(DSS)诱导的结肠炎的影响。通过给 C57BL/6 小鼠饮用 DSS 溶液诱导结肠炎 7 天后,用他克莫司处理这些动物。根据结肠单位长度的重量评估结肠炎症的严重程度。还测量了用他克莫司或载体处理的结肠炎小鼠分离的发炎结肠中释放的细胞因子(干扰素(IFN)-γ、白细胞介素(IL)-1β、IL-2、IL-4、IL-5、IL-6、IL-12 和肿瘤坏死因子(TNF)-α)的水平。与用载体处理的小鼠相比,用他克莫司治疗 14 天可降低单位长度结肠的重量,并抑制结肠炎小鼠发炎结肠中 IFN-γ 和 IL-1β的释放,但不抑制其他细胞因子。单位长度结肠的重量与 IFN-γ 或 IL-1β 的释放水平呈正相关。在单次给予他克莫司后,结肠炎小鼠的 IFN-γ 和 IL-1β 的释放也受到抑制。综上所述,这些结果表明他克莫司通过抑制发炎结肠中 IFN-γ 和 IL-1β 的释放来改善 DSS 诱导的结肠炎。