Takeshita M, Sugita T, Takata I
Marugo Research Service, Tanabe Seiyaku Co., Ltd., Osaka, Japan.
Exp Anim. 1997 Apr;46(2):165-9. doi: 10.1538/expanim.46.165.
The effects of anti-rheumatic drugs (dexamethasone 0.1 mg/kg and naproxen 5 mg/kg) were evaluated immunologically and histopathologically on type II collagen-induced arthritis in Lewis rats. Increased paw volume in the hind limbs was significantly suppressed in the groups treated with dexamethasone or naproxen, but noticeable retardation of body weight gain was observed in the group treated with dexamethasone. Serum anti-type II collagen IgG was significantly suppressed in the group treated with dexamethasone but not naproxen. Histopathological evaluation by our grading system, classification of the stages in arthritic lesion development, revealed suppression of the inflammatory changes in the tarsal joints of the animals treated with dexamethasone or naproxen. From our results, histopathological evaluation is considered to be more suitable for assessment of the efficacy of anti-rheumatic drugs on type II collagen-induced arthritis, an animal model for human rheumatoid arthritis.
在Lewis大鼠中,通过免疫和组织病理学方法评估了抗风湿药物(地塞米松0.1mg/kg和萘普生5mg/kg)对II型胶原诱导性关节炎的作用。地塞米松或萘普生治疗组后肢爪体积增加明显受到抑制,但地塞米松治疗组出现明显的体重增加迟缓。地塞米松治疗组血清抗II型胶原IgG明显受到抑制,而萘普生治疗组则未受抑制。通过我们的分级系统进行组织病理学评估,即对关节炎病变发展阶段进行分类,结果显示地塞米松或萘普生治疗的动物跗关节炎症变化受到抑制。根据我们的结果,组织病理学评估被认为更适合评估抗风湿药物对II型胶原诱导性关节炎(一种人类类风湿性关节炎动物模型)的疗效。