Human red blood cells were incubated in the presence of Na2MoO4 and th
e initial rate of molybdenum uptake was measured by using inductively
coupled plasma emission spectroscopy. About 99% of molybdenum uptake w
as inhibited by DIDS or by SITS. DIDS-sensitive molybdenum uptake was
inhibited by external chloride, bicarbonate, sulphate and phosphate in
the range of concentrations previously described for anion carrier fl
uxes. Trace elements, previously described to be translocated by the a
nion carrier, i. e. copper, zinc and cadmium, slightly inhibited molyb
denum uptake. Molybdenum uptake was strongly stimulated by acidificati
on, suggesting that the monovalent HMoO4- anion species, which is form
ed in acidic media (pK almost-equal-to 4.1), can be more rapidly trans
located than the divalent anion complex MoO42-, which is the predomina
nt form at physiological pH. In conclusion, the anion carrier can cata
lyse rapid molybdenum movements across red cells membranes. This suppo
rts previous reports of an enterohepatic circulation of molybdenum, wi
th red blood cells acting as molybdenum carrier between the intestine
and the liver.