Novotná J, Krabcová M, Deyl Z, Adam M
Cas Lek Cesk. 1989 Jan 6;128(2):41-5.
Gold complexes are used in the treatment of rheumatoid arthritis for some 60 years by now. The authors used therefore a gold complex, sodium aurothiosulphate (ATSS) to influence the experimental model of arthritis induced by immunization with type II collagen in laboratory rats. To the first group of laboratory rats ATSS was administered concurrently with the first immunization dose, to the second group with the second immunization dose and to the third group in the course of arthritis. ATSS was administered to individual groups every week by the i. m. route, 20 mg/kg body weight. In all three groups a reduction of arthritic symptoms was observed, however, in group three to a much lesser extent than in groups one and two. The results of the experiment indicate clearly that ATSS was able to suppress the development of collagen induced arthritis, if administered not later than with the second immunization dose. As the formation of antibodies against type II collagen was not suppressed, it may be assumed that the activation of the complement system was blocked by the bond of the gold complex with the C1q component. It has been proved already previously that the interaction of C1q with gold complexes is very rapid.
到目前为止,金配合物已用于治疗类风湿性关节炎约60年。因此,作者使用了一种金配合物——硫代硫酸金钠(ATSS)来影响实验室大鼠中由II型胶原免疫诱导的关节炎实验模型。将ATSS与首次免疫剂量同时给予第一组实验室大鼠,与第二次免疫剂量同时给予第二组,在关节炎病程中给予第三组。通过肌肉注射途径每周给各个组给予ATSS,剂量为20mg/kg体重。在所有三组中均观察到关节炎症状减轻,然而,第三组的减轻程度远低于第一组和第二组。实验结果清楚地表明,如果不迟于第二次免疫剂量给予ATSS,它能够抑制胶原诱导的关节炎的发展。由于抗II型胶原抗体的形成未被抑制,因此可以推测金配合物与C1q成分的结合阻断了补体系统的激活。先前已经证明C1q与金配合物的相互作用非常迅速。