Pathobiology of copper toxicity
Open Access
- 1 September 1984
- journal article
- review article
- Published by Taylor & Francis in Veterinary Quarterly
- Vol. 6 (4) , 179-235
- https://doi.org/10.1080/01652176.1984.9693935
Abstract
A review is presented of various aspects of copper (Cu) metabolism. The Cu absorption from the gastrointestinal tract in monogastric animals differs from that in ruminants. This is influenced by Cu binding compounds, sulphide production in the rumen, and molybdenum and zinc concentrations of the diet. Moreover, the valence of the Cu ions may influence the availability of Cu in the intestine. Metallothionein and lysosomes are involved in the accumulation of copper in the liver. The different findings in various Cu storage diseases may reflect different mechanisms of disease. Cu‐induced liver cell damage and haemolysis may be the result of lipid peroxidation.Keywords
This publication has 26 references indexed in Scilit:
- 3 years of continuous oral zinc therapy in 4 patients with Wilson's diseaseActa Neurologica Scandinavica, 2009
- Hepatic lysosomal copper protein in dogs with an inherited copper toxicosisHepatology, 1981
- LIPID PEROXIDATION AND THE CYTOTOXICITY OF COPPER*Annals of the New York Academy of Sciences, 1980
- THE ROLE OF THIOMOLYBDATES IN THE NUTRITIONAL INTERACTIONS OF COPPER, MOLYBDENUM, AND SULFUR: FACT OR FANTASY?Annals of the New York Academy of Sciences, 1980
- A kinetic model of copper metabolism in sheepAustralian Journal of Agricultural Research, 1980
- Excretion of Intravenously Injected Copper‐64 in SheepActa Pharmacologica et Toxicologica, 1978
- Protective effect of zinc supplementation against copper toxicosis in sheepBritish Journal of Nutrition, 1976
- A technique for measuring the biological availability of copper of sheep, sing hypocupraemic ewesBritish Journal of Nutrition, 1974
- Defective biliary excretion of copper in Wilson's diseaseGut, 1974
- The nature of the copper complexes in bile and their relationship to the absorption and excretion of copper in normal subjects and in Wilson's diseaseGut, 1973