Phytate, inositol hexaphosphate (InsP(6)), may be hydrolyzed to inositol ph
osphates with lower degree of phosphorylation, i.e., inositol penta- to mon
ophosphates (InsP(5)-InsP(1)), during food processing. Each of these lower
inositol phosphates exists in different isomeric forms. The objective of th
is study was to determine if different isomers of InsP(3)-InsP(5), (Ins(1,2
,4)P-3, ms(1,2,3)P-3, Ins(1,2,6)P-3, Ins(1,3,4)P-3, Ins(1,2,3,4)P-4, Ins(1,
2,5,6)P-4, Ins(1,2,4,5,6)P-5, and Ins(1,3,4,5,6)P-5) and InsP(6) affect the
uptake of iron. We studied the iron absorption in vitro using the human in
testinal epithelial cell line, Caco-2. Addition of a 2-fold molar excess of
InsP(6) or InsP(5) in proportion to Fe (1 h incubation at 37 degrees C) re
duced iron uptake by 46-52% (p < 0.001). Neither InsP(4) isomers nor InsP(3
) isomers affected iron uptake significantly at 1 h incubation with a molar
InsP:Fe level of 2:1. Iron uptake was shown to not be a function of the is
omeric form of inositol phosphates. The inositol phosphate isomers did not
seem likely to interact with each other through iron to form more stable ir
on complexes. At a molar InsP:Fe level of 20:1 an inhibitory effect of InsP
(4) was found, while InsP(3) did not affect the iron absorption even at a 2
0-fold molar excess.