Binysh S G, Eisen V
Arch Int Pharmacodyn Ther. 1981 Jan;249(1):126-36.
The effects of the gold salt sodium aurothiomalate and of d-penicillamine on complement were studied in vitro. Total haemolytic complement was inhibited by 0.05-1mM gold. The inhibitory potency of gold was inversely correlated to the concentration of complement in the system, but was not diminished by albumin or decomplemented serum protein in concentrations approaching those circulating in blood. Penicillamine which itself slightly inhibited complement, prevented or reversed the action of gold. Conversion of C1s to C1esterase was not inhibited. Gold inhibited the action of C1esterase on component C4, but not the action on small-molecular synthetic ester substrates. Only very high gold concentrations (375-560 microM) inhibited the conversion of C3 to C3b. No inhibition of the alternative pathway was detected.
体外研究了硫代苹果酸金钠和d-青霉胺这两种金盐对补体的影响。总溶血补体被0.05 - 1mM的金抑制。金的抑制效力与体系中补体的浓度呈负相关,但在接近血液中循环浓度的白蛋白或去补体血清蛋白存在时,其抑制作用并未减弱。本身对补体有轻微抑制作用的青霉胺可预防或逆转金的作用。C1s向C1酯酶的转化未受抑制。金抑制C1酯酶对C4成分的作用,但不抑制其对小分子合成酯底物的作用。只有非常高浓度的金(375 - 560 microM)才会抑制C3向C3b的转化。未检测到对替代途径的抑制作用。