In an attempt to define a tolerable daily intake (TDI) for molybdenum based
on a toxicological risk analysis approach, a large literature survey was c
onducted. In man, absorption of molybdenum after oral intake is in the rang
e of 28-77% and urinary excretion is 17-80% of the total dose. A low order
of toxicity of molybdenum compounds has been observed in humans. However, w
ith the available data, it is not possible to calculate any dose-response o
l dose-effect relationships. Because molybdenum toxicity is associated with
copper intake or depleted copper stores in the body, humans who have an in
adequate intake of dietary copper or some dysfunction in their copper metab
olism that makes them copper-deficient could be at greater risk of molybden
um toxicity, In the absence of relevant human studies, animal studies were
evaluated for the derivation of the TDI. Effects of Mo on reproduction and
foetal development were found to be critical effects observed in rats and m
ice. A dose-response relationship was observed in a study by Fungwe et al,,
with a 'no observed adverse effect' level (NOAEL) and a 'lowest observed a
dverse effect' level (LOAEL) of 0.9 and 1.6 mg Mo kg(-1) day(-1), respectiv
ely. Applying uncertainty factors of 10 for intraspecies and 10 for intersp
ecies differences to the NOAEL, a TDI of 0.009 mg Mo kg(-1) day(-1) was cal
culated, The TDI is given a medium confidence rating. This TDI is more than
double the upper limit of adequate intake for adolescents and adults that
was derived from the Mo content of the average diet in the USA. Copyright (
C) 1999 John Wiley & Sons, Ltd.