Arita C, Kaibara N, Hotokebuchi T, Takagishi K, Arai K
Clin Immunol Immunopathol. 1987 Jun;43(3):354-61. doi: 10.1016/0090-1229(87)90145-0.
The effects of cyclophosphamide (CY) and its structurally related analogs, ifosfamide (Ifo), sufosfamide (Sufo), and mafosfamide (Mafo), on collagen arthritis in Sprague-Dawley rats were examined. Prophylactic treatment with 7.5-10 mg/kg/day of CY. 15 mg/kg/day of Ifo, and 10-15 mg/kg/day of Sufo for the first 10 days starting on the same day as the type II collagen immunization suppressed arthritis induction as well as humoral immune response to type II collagen. Prophylactic treatment with Mafo at doses ranging from 10 to 40 mg/kg/day for 10 days was ineffective in suppressing the disease development. When drug treatment was started only during the immediate preclinical phase of arthritis, the development of arthritis was suppressed in the animals treated with 10 mg/kg/day of CY and 15 mg/kg/day of Ifo from Day 5 to Day 14. Additional studies demonstrated that treatment with 10 mg/kg/day of CY and 15 mg/kg/day of Ifo started at the time of disease onset significantly suppressed the severity of arthritis compared with the control group. These results show the effectiveness of Ifo and CY on this animal model of polyarthritis and suggest the possibility of clinical use of Ifo for the treatment of human arthritides similar to CY.
研究了环磷酰胺(CY)及其结构相关类似物异环磷酰胺(Ifo)、硫磷酰胺(Sufo)和马磷酰胺(Mafo)对斯普拉格-道利大鼠胶原性关节炎的影响。从Ⅱ型胶原免疫接种当天开始的前10天,以7.5 - 10mg/kg/天的CY、15mg/kg/天的Ifo和10 - 15mg/kg/天的Sufo进行预防性治疗,可抑制关节炎的诱导以及对Ⅱ型胶原的体液免疫反应。以10至40mg/kg/天的剂量给予Mafo进行10天的预防性治疗,在抑制疾病发展方面无效。当仅在关节炎的临床前期开始药物治疗时,从第5天至第14天,用10mg/kg/天的CY和15mg/kg/天的Ifo治疗的动物中关节炎的发展受到抑制。进一步的研究表明,与对照组相比,在疾病发作时开始用10mg/kg/天的CY和15mg/kg/天的Ifo治疗可显著抑制关节炎的严重程度。这些结果显示了Ifo和CY对这种多关节炎动物模型的有效性,并提示Ifo在临床上用于治疗与CY类似的人类关节炎的可能性。