Bonkowsky H L, Carpenter S J, Healey J F
Arch Pathol Lab Med. 1979 Jan;103(1):21-9.
To understand better the intracellular iron distribution and metabolic consequences of chronic hepatic iron overload, rats were given large doses of iron dextran or ferric citrate intraperitoneally. They accumulated large quantities of iron within Kupffer cells and hepatocytes. The relative subcellular iron distributions were similar in controls and iron-loaded rats, despite a ten- to 20-fold difference in hepatic iron concentration. Electron microscopy of whole liver and subcellular particulate fractions suggested that iron was present in highest concentration in lysosomes, which were rendered more labile by its presence. Nevertheless, quantitative iron determinations on all subcellular fractions, obtained by two preparative methods, showed that most of the iron was present in the "soluble" fraction. The amount of iron in the "microsomal" fraction varied, depending on the techniques used for preparation of this fraction. Cytochrome P-450 and total heme concentrations were decreased 40% to 50% in microsomes isolated from iron-loaded livers.
为了更好地理解慢性肝铁过载的细胞内铁分布及代谢后果,给大鼠腹腔注射大剂量的右旋糖酐铁或柠檬酸铁。它们在库普弗细胞和肝细胞内积累了大量的铁。尽管肝铁浓度相差10至20倍,但对照组和铁负荷大鼠的相对亚细胞铁分布相似。对全肝和亚细胞颗粒组分进行电子显微镜检查表明,溶酶体中铁的浓度最高,铁的存在使其变得更不稳定。然而,通过两种制备方法对所有亚细胞组分进行的定量铁测定表明,大部分铁存在于“可溶性”组分中。“微粒体”组分中的铁含量因制备该组分所用的技术而异。从铁负荷肝脏分离的微粒体中,细胞色素P-450和总血红素浓度降低了40%至50%。