Nederbragt H, Lagerwerf A J
Hepatology. 1986 Jul-Aug;6(4):601-7. doi: 10.1002/hep.1840060409.
Biliary copper excretion was studied in male, bile-cannulated rats of the inbred strains Fischer, Brown Norway, WAG/Rij and Lewis. After intravenous injection of 10, 30 and 50 micrograms copper per 100 gm body weight, two patterns of copper excretion were observed; their profiles varied with the copper dose and the strain of the rats used. The lowest amounts of copper were excreted by Fischer rats, the highest by WAG/Rij rats; this was related to the effect of the copper dose on both patterns. The subcellular distribution of copper in the liver was studied in Fischer and Brown Norway rats after doses of 50, 100, and 200 micrograms per 100 gm body weight. Brown Norway rats accumulated more copper in the liver, although the copper concentration was the same in both strains 1 hr after injection of all doses. Fischer rats accumulated proportionally more copper in lysosomal and nuclear mitochondrial fractions whereas Brown Norway rats accumulated proportionally more copper in the cytosol. Gel filtration of liver supernatants revealed that the amount of copper accumulating in the protein presumed to be metallothionein was 2 to 3 times higher in Brown Norway rats, whereas in the Fischer rats more copper eluted in the void volume fraction. We conclude that both biliary copper excretion and copper distribution in the liver are under genetic control. Because of its low copper excretion and reduced binding of copper to metallothionein the Fischer rat, compared to other strains, may be a suitable model for studying the involvement of the liver in copper intoxication.
在雄性、胆管插管的近交系大鼠(Fischer、棕色挪威大鼠、WAG/Rij和Lewis)中研究了胆汁铜排泄情况。静脉注射每100克体重10、30和50微克铜后,观察到两种铜排泄模式;它们的曲线随铜剂量和所用大鼠品系而变化。Fischer大鼠排泄的铜量最低,WAG/Rij大鼠排泄的铜量最高;这与铜剂量对两种模式的影响有关。在Fischer和棕色挪威大鼠中,研究了每100克体重给予50、100和200微克铜剂量后肝脏中铜的亚细胞分布。棕色挪威大鼠在肝脏中积累了更多的铜,尽管在注射所有剂量后1小时,两种品系的铜浓度相同。Fischer大鼠在溶酶体和核线粒体部分按比例积累更多的铜,而棕色挪威大鼠在胞质溶胶中按比例积累更多的铜。肝脏上清液的凝胶过滤显示,棕色挪威大鼠中假定为金属硫蛋白的蛋白质中积累的铜量高2至3倍,而在Fischer大鼠中,更多的铜在空体积部分洗脱。我们得出结论,胆汁铜排泄和肝脏中的铜分布均受遗传控制。由于Fischer大鼠铜排泄量低且铜与金属硫蛋白的结合减少,与其他品系相比,它可能是研究肝脏在铜中毒中作用的合适模型。