In adult humans, the net absorption of dietary copper is approximate t
o 1 mg/d. Dietary copper joins some 4-5 mg of endogenous copper flowin
g into the gastrointestinal tract through various digestive juices. Mo
st of this copper returns to the circulation and to the tissues (inclu
ding liver) that formed them. Much lower amounts of copper flow into a
nd out of other major parts of the body (including heart, skeletal mus
cle, and brain). Newly absorbed copper is transported to body tissues
in two phases, borne primarily by plasma protein carriers (albumin, tr
anscuprein, and ceruloplasmin). In the first phase, copper goes from t
he intestine to the liver and kidney; in the second phase, copper usua
lly goes from the liver land perhaps also the kidney) to other organs.
Ceruloplasmin plays a role in this second phase. Alternatively, liver
copper can also exit via the bile, and in a form that is less easily
reabsorbed. Copper is also present in and transported by other body fl
uids, including those bathing the brain and central nervous system and
surrounding the fetus in the amniotic sac. Ceruloplasmin is present i
n these fluids and may also be involved in copper transport there. The
concentrations of copper and ceruloplasmin in milk vary with lactatio
nal stage. Parallel changes occur in ceruloplasmin messenger RNA expre
ssion in the mammary gland las determined in pigs). Copper in milk cer
uloplasmin appears to be particularly available for absorption, at lea
st in rats.