Mann J R, Camakaris J, Danks D M, Walliczek E G
Biochem J. 1979 Jun 15;180(3):605-12. doi: 10.1042/bj1800605.
Copper therapy was applied to brindled mouse mutants, which suffer from lethal hypocupraemia, by using cuprous and cupric solutions. The method of treatment was a single subcutaneous injection of 50 microgram of copper at 7 days of age. Early effects of the dose were: prevention of the tremors and spasms seen in untreated mutants, raising to normal and near-normal of caeruloplasmin oxidase and lysyl oxidase activities and pigmentation of skin and fur. Growth of mutants was retarded up to 23 days of age, but thereafter they rapidly gained weight to be nearly normal by 60 days of age. At 3 days after injection, copper concentrations in previously deficient mutant organs apart from liver were at least as much as those of treated normals, which had remained unchanged. Copper in mutant livers had increased only slightly in comparison with the normal control. A state of copper deficiency recurred in mutant tissues by 25 days after injection. A solution of Cu+, retained as such by an alkyl polyether, and sebacic acid resulted in greater growth rates after 23 days than did three other copper treatments. Cu+ may have resulted in an improved growth response owing to it being more readily metabolized than C12+. Delayed release of copper from the site of injection may have played an important role.
通过使用亚铜溶液和铜溶液,对患有致死性低铜血症的花斑小鼠突变体进行了铜疗法。治疗方法是在7日龄时皮下注射50微克铜。该剂量的早期效果包括:预防未治疗突变体中出现的震颤和痉挛,使血浆铜蓝蛋白氧化酶和赖氨酰氧化酶活性恢复到正常和接近正常水平,以及皮肤和毛发色素沉着。突变体的生长在23日龄前受到抑制,但此后它们迅速增重,到60日龄时体重接近正常。注射后3天,除肝脏外,先前缺乏铜的突变体器官中的铜浓度至少与经治疗的正常小鼠相同,而正常小鼠的铜浓度保持不变。与正常对照相比,突变体肝脏中的铜仅略有增加。注射后25天,突变体组织中再次出现铜缺乏状态。一种由烷基聚醚原样保留的Cu⁺溶液和癸二酸,在23天后导致的生长速率比其他三种铜处理方法更高。Cu⁺可能由于比Cu²⁺更易于代谢而导致生长反应改善。铜从注射部位的延迟释放可能起到了重要作用。