Rungby J, Hultman P, Ellermann-Erikson S
Arch Toxicol. 1987 Apr;59(6):408-12. doi: 10.1007/BF00316206.
The effects of silver on cultured mouse peritoneal macrophages were examined by estimation of cell survival and by light and electron microscopy. Addition of silver lactate to the culture medium at final concentrations of 40 and 80 microM resulted in coagulation necrosis and rapid cell death. At lower concentrations cell structure appeared normal. However, the rate of cell death at 20 microM silver lactate was increased as compared to controls. Silver, visualized by physical development/autometallography, was invariably located in lysosomes. The production of malondialdehyde in mouse liver of silver-treated mice as compared to controls was also examined. This lipid peroxidation product had increased to the same amount in animals treated with silver for either 3 days or with only one silver injection 4 h before examination. This study has demonstrated that silver affects viability and structure of cultured macrophages, possibly due to induction of lipid peroxidation, as demonstrated to occur in the liver of silver-exposed mice.
通过评估细胞存活率以及光学和电子显微镜观察,研究了银对培养的小鼠腹腔巨噬细胞的影响。在培养基中添加终浓度为40和80微摩尔的乳酸银会导致凝固性坏死和细胞快速死亡。在较低浓度下,细胞结构看起来正常。然而,与对照组相比,20微摩尔乳酸银处理组的细胞死亡率有所增加。通过物理显影/自动金属显影观察到的银始终位于溶酶体中。还检测了与对照组相比,经银处理的小鼠肝脏中丙二醛的产生情况。在接受银处理3天的动物或在检查前4小时仅注射一次银的动物中,这种脂质过氧化产物的含量增加到相同水平。本研究表明,银会影响培养的巨噬细胞的活力和结构,这可能是由于诱导脂质过氧化所致,正如在接触银的小鼠肝脏中所观察到的那样。