TISSUE TURNOVER OF ALUMINUM AND GA-67 - EFFECT OF IRON STATUS

Citation
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
Citations number
34
Categorie Soggetti
Medicine, Research & Experimental
ISSN journal
00379727
Volume
207
Issue
1
Year of publication
1994
Pages
89 - 96
Database
ISI
SICI code
0037-9727(1994)207:1<89:TTOAAG>2.0.ZU;2-K
Abstract
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.