Copper [Cu]
Overview
Macro clinical perspective
Cu is only needed in only trace amounts in humans. Total Cu in the body is >100 mg1. The skeleton and muscles account for 1/2 of the Cu in the body1.
Most Cu in the body exists copper almost always exists in biological systems bound to proteins1. Free copper in cells and in the body is extremely low1
High [Cu] is related to metabolic activity of organs1. Kidney and liver have the highest [Cu], followed by the brain (~5 µg/g), then the heart1.
Copper metabolism
Copper absorption
Copper absorption is considerably higher than for that of other trace elements (~55-75%)1
Relative amount of copper in the diet seems to be inversely correlated with percent intestinal absorption1. Percent absorption increases during states of deficiency1.
Copper absorption occurs mainly in the upper small intestine1
Copper Bioavailability
Function
Through copper’s enzymes (Multi-copper oxidases) copper has the unique ability to convert O2 into H2O without producing oxidative “exhaust”2. This allows our bodies to manage O2 without being negatively affected by its toxic and highly reactive nature2
Metabolic Functions
Copper plays a crucial role in energy transformation in the body1. Copper impacts this process by acting as a cofactor for cytochrome c oxidase (Terminal enzyme in the electron transport chain)1
Iron utilization
Copper is important in the normal utilization of iron in the body1. From Intestinal iron absorption, iron release from stores (e.g. in macrophages of liver and spleen), iron incorporation into hemoglobin, and even preventing anemia1.
Vascular function
Cardiac function
- Cross-linking of CT in heart1
Skeleton
- Cross-linking of CT in bones1
Oxidative damage defense
- Defense against oxidative damage1
Myelination
- Myelination of brain and spinal cord1
Reproduction
- Copper has a function in reproduction1
Hormone synthesis
- Copper plays a role in hormone synthesis1
Multi-Copper Oxidases (MCOs)
3 Multi-Copper oxidases have been detected in humans:2
All 3 of these enzymes have a high specificity towards iron with the resulting ferroxidase activity being associated with ferroportin (the only known iron exporter protein in humans.)2
Ferroportin exports iron as Fe2+, but transferrin, the major iron transporter protein of blood, can bind only Fe3+ effectively. Iron oxidation in enterocytes is mediated mainly by hephaestin thus allowing dietary iron to enter the bloodstream2
Ceruloplasmin
Function: Release of iron from the liver relies on ferroportin and the ferroxidase activity of ceruloplasmin which is found in blood in a soluble form2
Hephaestin
Iron oxidation in enterocytes is mediated mainly by hephaestin thus allowing dietary iron to enter the bloodstream2
Zyklopen
Zyklopen is involved in iron efflux from placental trophoblasts during iron transfer from mother to fetus2
Deficiency
Copper deficiency can result in peripheral neuropathies3