Baggott J E, Morgan S L, Freeberg L E, Hudson B B, Vaughn W H, Gopal Nair M, Krumdieck C L, Koopman W J, Gay R E, Gay S
Department of Nutrition Sciences, University of Alabama, Birmingham 35294.
Agents Actions. 1992 Jan;35(1-2):104-11. doi: 10.1007/BF01990959.
Female MRL/lpr mice were treated with I.P. doses of methotrexate (MTX) and 10-deazaaminopterin (DAAM) in the range of 1 to 100 mg/kg body weight/week, in two equally divided doses. Treatment began at 7 weeks of age and continued to 30 weeks of age. Joint histopathology scores were tightly correlated with skin lesion-proteinuria scores at 30 weeks of age. MTX at levels of 5, 25, and 100 mg/kg body weight/week and DAAM at a level of 25 mg/kg body weight/week significantly reduced skin lesion-proteinuria scores below controls in a dose dependent manner. Animals receiving MTX at 25 mg/kg body weight/week had a significantly longer median life span and animals receiving MTX at 100 mg/kg body weight/week had a greater than 15% suppression of growth when compared with controls. Longevity and skin lesion-proteinuria scores appeared to be good indicators of drug efficacy while growth suppression appeared to be a good indicator of drug toxicity.
雌性MRL/lpr小鼠腹腔注射甲氨蝶呤(MTX)和10-脱氮氨基蝶呤(DAAM),剂量范围为每周1至100毫克/千克体重,分两次等量注射。治疗从7周龄开始,持续到30周龄。30周龄时,关节组织病理学评分与皮肤病变-蛋白尿评分密切相关。每周体重5、25和100毫克/千克的MTX以及每周体重25毫克/千克的DAAM以剂量依赖方式显著降低皮肤病变-蛋白尿评分,低于对照组。与对照组相比,每周接受25毫克/千克体重MTX的动物中位寿命显著延长,每周接受100毫克/千克体重MTX的动物生长抑制超过15%。寿命和皮肤病变-蛋白尿评分似乎是药物疗效的良好指标,而生长抑制似乎是药物毒性的良好指标。