Copper [Cu]

Authors
Affiliations

Doctor of Physical Therapy

B.S. in Kinesiology

Doctor of Physical Therapy

B.A. in Neuroscience

Overview

  • Copper(Cu) is the 26th element in abundance in the crust of the earth.
  • 29th periodic element
  • 2 stable and 9 radioactive isotopes

Macro clinical perspective

  • Cu is only needed in only trace amounts in humans. Total Cu in the body is >100 mg. The skeleton and muscles account for 1/2 of the Cu in the body.

  • Most Cu in the body exists copper almost always exists in biological systems bound to proteins. Free copper in cells and in the body is extremely low

  • High [Cu] is related to metabolic activity of organs. Kidney and liver have the highest [Cu], followed by the brain (~5 µg/g), then the heart.

Copper metabolism

Copper absorption

  • Copper absorption is considerably higher than for that of other trace elements (~55-75%)

  • Relative amount of copper in the diet seems to be inversely correlated with percent intestinal absorption. Percent absorption increases during states of deficiency.

  • Copper absorption occurs mainly in the upper small intestine

Copper Bioavailability

  • Dietary factors (i.e. iron, vitamin C, and Zinc) have been reported to exert adverse effects on the bioavailability of copper

  • Other factors impact Copper’s bioavailability, such as lead poisoning, hemochromatosis, and excessive ingestion of soft drinks

Function

Through copper’s enzymes (Multi-copper oxidases) copper has the unique ability to convert O2 into H2O without producing oxidative “exhaust”. This allows our bodies to manage O2 without being negatively affected by its toxic and highly reactive nature

Metabolic Functions

Copper plays a crucial role in energy transformation in the body. Copper impacts this process by acting as a cofactor for cytochrome c oxidase (Terminal enzyme in the electron transport chain)

Iron utilization

Copper is important in the normal utilization of iron in the body. From Intestinal iron absorption, iron release from stores (e.g. in macrophages of liver and spleen), iron incorporation into hemoglobin, and even preventing anemia.

Vascular function

  • Blood coagulation is assisted by copper.
  • Blood pressure control
  • Cross-linking of connective tissues in arteries

Cardiac function

  • Cross-linking of CT in heart

Skeleton

  • Cross-linking of CT in bones

Oxidative damage defense

  • Defense against oxidative damage

Myelination

  • Myelination of brain and spinal cord

Reproduction

  • Copper has a function in reproduction

Hormone synthesis

  • Copper plays a role in hormone synthesis

Multi-Copper Oxidases (MCOs)

3 Multi-Copper oxidases have been detected in humans:

  1. Ceruloplasmin
  2. Hephaestin
  3. Zyklopen

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.)

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 bloodstream

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 form

Hephaestin

Iron oxidation in enterocytes is mediated mainly by hephaestin thus allowing dietary iron to enter the bloodstream

Zyklopen

Zyklopen is involved in iron efflux from placental trophoblasts during iron transfer from mother to fetus

Deficiency

Copper deficiency can result in peripheral neuropathies

References

1.
Collins JF, Klevay LM. Copper. Advances in Nutrition (Bethesda, Md). 2011;2(6):520-522. doi:10.3945/an.111.001222
2.
Vashchenko G, MacGillivray RTA. Multi-copper oxidases and human iron metabolism. Nutrients. 2013;5(7):2289-2313. doi:10.3390/nu5072289
3.
Amato AA, Russell JA. Neuromuscular Disorders. 2nd ed. McGraw-Hill Education; 2016.

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