TY - JOUR
T1 - Bioavailability of aluminum from drinking water
AU - Fulton, Barbara
AU - Jaw, Sarah
AU - Jeffery, Elizabeth H.
N1 - Funding Information:
’ This work was supported by USGS, WRC Grant S-112. Presented in part at the Annual Meeting of the Society of Toxicology in Dallas, TX, February 1988.
PY - 1989/1
Y1 - 1989/1
N2 - Bioavailability of Aluminum from Drinking Water. FULTON, B., JAW, S., AND JEFFERY, E. H. (1989). Fundam Appl. Toxicol. 12, 144-150. Aluminum, present in our drinking water as hydroxide or sulfate, is limited by solubility to 2.5 mg/liter at pH 7.0. This study was carried out to determine if aluminum at doses typically found in drinking water would accumulate in rat tissues if a ligand such as citrate at neutral or acid pH is coadministered, or in the absence of citrate at acid pH. Al(OH)3 or AlCl3 was given ad libitum in drinking water to male Sprague-Dawley rats at 0, 0.1, 2.0, or 100 mg/liter, in 4 mM acetate, pH 3.2 (A), 4 mM citrate, pH 2.6 (C), 4 mM citrate, pH 7.0 (7C), or distilled water, pH 7.0(W). After 10 weeks, rats were killed and tissues were wet-ashed in nitric acid for determination of aluminum by flameless atomic absorption. Copper, iron, and zinc were determined by flame atomic absorption. Metal ion concentrations in tibia, brain, liver, blood, and kidney did not differ significantly between treatment groups. Aluminum accumulated in intestinal cells of all 100 mg Al/liter rats, with the C group accumulating more aluminum than the A or W groups. In the C group, intestinal aluminum content increased significantly in a dose-dependent manner. Intestinal iron was decreased significantly in all the 100 mg Al/liter groups. Intestinal copper was decreased in the W group at 100 mg Al/liter, with a trend toward a decrease in A and C groups. We conclude that at these low levels studied, aluminum accumulates in intestinal tissue, and that this accumulation is enhanced by citrate ligand. At 100 mg Al/liter, intestinal iron accumulation is decreased, and copper accumulation is marginally decreased.
AB - Bioavailability of Aluminum from Drinking Water. FULTON, B., JAW, S., AND JEFFERY, E. H. (1989). Fundam Appl. Toxicol. 12, 144-150. Aluminum, present in our drinking water as hydroxide or sulfate, is limited by solubility to 2.5 mg/liter at pH 7.0. This study was carried out to determine if aluminum at doses typically found in drinking water would accumulate in rat tissues if a ligand such as citrate at neutral or acid pH is coadministered, or in the absence of citrate at acid pH. Al(OH)3 or AlCl3 was given ad libitum in drinking water to male Sprague-Dawley rats at 0, 0.1, 2.0, or 100 mg/liter, in 4 mM acetate, pH 3.2 (A), 4 mM citrate, pH 2.6 (C), 4 mM citrate, pH 7.0 (7C), or distilled water, pH 7.0(W). After 10 weeks, rats were killed and tissues were wet-ashed in nitric acid for determination of aluminum by flameless atomic absorption. Copper, iron, and zinc were determined by flame atomic absorption. Metal ion concentrations in tibia, brain, liver, blood, and kidney did not differ significantly between treatment groups. Aluminum accumulated in intestinal cells of all 100 mg Al/liter rats, with the C group accumulating more aluminum than the A or W groups. In the C group, intestinal aluminum content increased significantly in a dose-dependent manner. Intestinal iron was decreased significantly in all the 100 mg Al/liter groups. Intestinal copper was decreased in the W group at 100 mg Al/liter, with a trend toward a decrease in A and C groups. We conclude that at these low levels studied, aluminum accumulates in intestinal tissue, and that this accumulation is enhanced by citrate ligand. At 100 mg Al/liter, intestinal iron accumulation is decreased, and copper accumulation is marginally decreased.
UR - http://www.scopus.com/inward/record.url?scp=0024548690&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0024548690&partnerID=8YFLogxK
U2 - 10.1093/toxsci/12.1.144
DO - 10.1093/toxsci/12.1.144
M3 - Article
C2 - 2925013
AN - SCOPUS:0024548690
SN - 1096-6080
VL - 12
SP - 144
EP - 150
JO - Toxicological Sciences
JF - Toxicological Sciences
IS - 1
ER -