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甲氨蝶呤可抑制大鼠佐剂性关节炎中巨噬细胞的活化以及血管和细胞炎症反应。

Methotrexate inhibits macrophage activation as well as vascular and cellular inflammatory events in rat adjuvant induced arthritis.

作者信息

Johnson W J, DiMartino M J, Meunier P C, Muirhead K A, Hanna N

机构信息

Department of Immunology, Smith Kline and French Laboratories, King of Prussia, PA 19406.

出版信息

J Rheumatol. 1988;15(5):745-9.

PMID:3262750
Abstract

We demonstrated previously that variables of macrophage activation are associated with the development and progression of the arthritic lesion in the model of adjuvant induced arthritis. This association was investigated further by assessing the ability of antiarthritic agents to modulate variables of macrophage activation in direct comparison to effects on the arthritic lesion. Whereas indomethacin effectively reduced hindpaw edema, it had no significant effect on Ia expression or on any measurement of activation. Prednisolone inhibited hindpaw edema and the production of interleukin-1 (IL-1) by splenic macrophages. Only methotrexate inhibited hindpaw edema and all variables of macrophage activation (PGE2 and IL-1 production, cyanine dye accumulation) as well as the influx of Ia positive macrophages into synovial tissue.

摘要

我们之前证明,在佐剂诱导的关节炎模型中,巨噬细胞激活的变量与关节炎病变的发展和进展相关。通过评估抗关节炎药物调节巨噬细胞激活变量的能力,并与对关节炎病变的影响进行直接比较,对这种关联进行了进一步研究。吲哚美辛虽能有效减轻后爪水肿,但对Ia表达或任何激活指标均无显著影响。泼尼松龙抑制后爪水肿以及脾巨噬细胞产生白细胞介素-1(IL-1)。只有甲氨蝶呤抑制后爪水肿、巨噬细胞激活的所有变量(前列腺素E2和IL-1产生、花青染料蓄积)以及Ia阳性巨噬细胞向滑膜组织的流入。

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