Jl. Greger et al., TISSUE TURNOVER OF ALUMINUM AND GA-67 - EFFECT OF IRON STATUS, Proceedings of the Society for Experimental Biology and Medicine, 207(1), 1994, pp. 89-96
The purposes of this study were to evaluate the effect of nutritional
status in regard to iron an aluminum distribution and turnover and to
evaluate Ga-67 as a marker for aluminum. Anemic (n = 27) and normal (n
= 30) rats were dosed by gavage with 0.8 mmoles of aluminum and 20 mu
Ci Ga-67 in a 0.75 mol/l citrate solution and sacrificed 1, 3, 6, 9,
15, and 21 days later. Anemic rats generally retained more aluminum in
their livers but less in tibias and spleens than normal rats. The hal
f-lives of aluminum in liver (56 vs 17 days), muscle (33 vs 16 days),
and serum (12 vs 8 days) were significantly greater in anemic than nor
mal rats, respectively. Total body retention of Ga-67 could be describ
ed on the basis of a two-compartment model. The turnover of Ga-67 from
the first compartment was rapid (half-life = 0.8 and 0.6 days) in ane
mic and normal rats, respectively, and was similar to the turnover of
Ga-67 from the GI tract (half-life = 0.7 and 0.6 days in anemic and no
rmal rats, respectively). The turnover of Ga-67 from the second compar
tment was also rapid (2.8 vs 4.0 days in anemic and normal rats, respe
ctively). Anemia affected the retention of Ga-67 more than the retenti
on of aluminum; anemic rats retained more Ga-67 in their livers, splee
ns, kidneys, hearts, and muscles but less in their tibias than normal
rats. In general, Ga-67 was not a satisfactory marker for aluminum dis
tribution and turnover in normal and anemic rats.