P. Jouhanneau et al., GASTROINTESTINAL ABSORPTION, TISSUE RETENTION, AND URINARY-EXCRETION OF DIETARY ALUMINUM IN RATS DETERMINED BY USING AL-26, Clinical chemistry, 43(6), 1997, pp. 1023-1028
We used accelerator mass spectrometry (AMS) and Al-26 to study the pla
sma concentration, urinary excretion, and retention in bone, brain, an
d liver of a single dose of a dietary concentration of aluminum ingest
ed either with or without citrate by 2-month-old Wistar rats. In the a
bsence of citrate, cumulative urinary excretion and skeleton retention
were each similar to 0.05% of the total Al-26 dose ingested. Al-26 re
tention in brain and liver were similar to 4 x 10(-8) and 2 x 10(-6),
respectively. Concomitant citrate intake increased these median values
by about two- to fivefold, although this factor was highly variable i
n individual rats. Independent of citrate administration, 90% of the A
l-26 excreted in urine (measured cumulatively over 30 days) was excret
ed within the first 48 h. Uptake by bone was rapid (similar to 1 h) an
d permanent over the 30-day duration of the experiment.