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新型免疫抑制剂FTY720对大鼠佐剂性关节炎的影响。

Effect of FTY720, a novel immunosuppressant, on adjuvant-induced arthritis in rats.

作者信息

Matsuura M, Imayoshi T, Chiba K, Okumoto T

机构信息

Drug Development Laboratories, Welfide Corporation, Chikujo-gun, Fukuoka, Japan.

出版信息

Inflamm Res. 2000 Aug;49(8):404-10. doi: 10.1007/s000110050608.

Abstract

OBJECTIVE AND DESIGN

Anti-arthritic effect of FTY720, a novel immunosuppressant, was compared with those of immunosuppressants cyclosporin A and tacrolimus in adjuvant-induced arthritis in rats.

MATERIAL

Male LEW rats.

TREATMENT

FTY720 (0.03-0.3 mg/kg), cyclosporin A (1-10 mg/kg) or tacrolimus (0.3-3 mg/kg) were orally administered to rats for 21 days beginning on the day (day 0) of adjuvant inoculation. In addition, the anti-arthritic effect of FTY720 (0.3 mg/kg) and cyclosporin A (10 mg/kg) were evaluated by administration to animals for 5 consecutive days (days 2-6, 6-10, and 10-14).

METHODS

Adjuvant-induced arthritis was produced by intradermal injection of 0.5 mg heat-killed Mycobacterium tuberculosis. Hindpaw edema was measured plethysmographically. The day of arthritis onset was determined macroscopically. Bone degradation was determined by radiography. Peripheral blood leukocytes were classified microscopically.

RESULTS

All test compounds inhibited the incidence of arthritis, hindpaw edema and bone destruction. In addition, FTY720 but not cyclosporin A or tacrolimus markedly decreased the number of peripheral blood lymphocytes. FTY720 treatment on days 6 to 10 inhibited the bone destruction and hindpaw edema.

CONCLUSION

These results suggest that the anti-arthritic effect of FTY720 in this adjuvant-induced arthritic model was more potent than those of cyclosporin A and tacrolimus. FTY720 administered on days 6 to 10 showed the inhibitory effect on the bone destruction and hindpaw edema. FTY720 may be effective in the treatment of rheumatoid arthritis.

摘要

目的与设计

将新型免疫抑制剂FTY720的抗关节炎作用与免疫抑制剂环孢素A和他克莫司在佐剂诱导的大鼠关节炎中的作用进行比较。

材料

雄性LEW大鼠。

处理

从佐剂接种当天(第0天)开始,给大鼠口服FTY720(0.03 - 0.3毫克/千克)、环孢素A(1 - 10毫克/千克)或他克莫司(0.3 - 3毫克/千克),持续21天。此外,通过连续5天(第2 - 6天、第6 - 10天和第10 - 14天)给动物给药来评估FTY720(0.3毫克/千克)和环孢素A(10毫克/千克)的抗关节炎作用。

方法

通过皮内注射0.5毫克热灭活的结核分枝杆菌诱导佐剂性关节炎。用体积描记法测量后爪水肿。通过肉眼观察确定关节炎发作的日期。通过X射线摄影确定骨质破坏情况。通过显微镜对周边血白细胞进行分类。

结果

所有受试化合物均抑制关节炎的发生率、后爪水肿和骨质破坏。此外,FTY720能显著降低外周血淋巴细胞数量,而环孢素A和他克莫司则不能。在第6至10天给予FTY720治疗可抑制骨质破坏和后爪水肿。

结论

这些结果表明,在该佐剂诱导的关节炎模型中,FTY720的抗关节炎作用比环孢素A和他克莫司更强。在第6至10天给予FTY720对骨质破坏和后爪水肿有抑制作用。FTY720可能对类风湿关节炎的治疗有效。

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