Bramm E, Binderup L, Arrigoni-Martelli E
Acta Pharmacol Toxicol (Copenh). 1979 Jan;44(1):75-80. doi: 10.1111/j.1600-0773.1979.tb02297.x.
The effects of different antirheumatic drugs administered according to various dosing regimes on tuberculin hypersensitivity in rats have been assessed quantitating the changes of exudate volume and mononuclear cells immigration at the site of challenge. Dosing at the time of sensitization with aurothiomalate and D-penicillamine enhanced the cell immigration which was decreased by similar treatment with levamisole. Cyclophosphamide increased the exudate formation. Indomethacin had no effect. Dosing at the time of challenge caused a marked reduction of both the parameters by aurothiomalate and cyclophosphamide and enhancement by levamisole. D-penicillamine increased only the cellular immigration and indomethacin the exudate formation. Long treatment with aurothiomalate and cyclophosphamide suppressed the responses. Similar treatment with D-penicillamine and levamisole produced a significant enhancement. Indomethacin had no effect. The relevance of these findings to the testing and mode of action of antirheumatic drugs is discussed.
通过对攻击部位渗出液体积和单核细胞迁移变化进行定量,评估了按照不同给药方案给予不同抗风湿药物对大鼠结核菌素超敏反应的影响。在用金硫代苹果酸和D-青霉胺致敏时给药会增强细胞迁移,而左旋咪唑进行类似处理则会降低细胞迁移。环磷酰胺会增加渗出液形成。吲哚美辛无作用。在攻击时给药会使金硫代苹果酸和环磷酰胺导致的这两个参数显著降低,而左旋咪唑则会使其增强。D-青霉胺仅增加细胞迁移,吲哚美辛则增加渗出液形成。长期用金硫代苹果酸和环磷酰胺处理会抑制反应。用D-青霉胺和左旋咪唑进行类似处理会产生显著增强作用。吲哚美辛无作用。讨论了这些发现与抗风湿药物的测试及作用方式的相关性。