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Articles |
1
Centre de Spectrométrie Nucléaire et de Spectrométrie de Masse (CSNSM), CNRS-IN2P3, Bat 108, 91405 Orsay, France.
2
INSERM U 90, Hôpital Necker, Paris, France.
3
Département de Physiologie, Faculté de
Pharmacie, Châtenay-Malabry, France.
a Author for correspondence. Fax 33 1 69 15 52 68; e-mail raisbeck{at}csnsm.in2p3.fr
We used accelerator mass spectrometry (AMS) and 26Al to study the plasma concentration, urinary excretion, and retention in bone, brain, and liver of a single dose of a dietary concentration of aluminum ingested either with or without citrate by 2-month-old Wistar rats. In the absence of citrate, cumulative urinary excretion and skeleton retention were each ~0.05% of the total 26Al dose ingested. 26Al retention in brain and liver were ~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 in individual rats. Independent of citrate administration, 90% of the26Al excreted in urine (measured cumulatively over 30 days) was excreted within the first 48 h. Uptake by bone was rapid (~1 h) and permanent over the 30-day duration of the experiment.
Key Words: indexing terms: mass spectrometry rats citrate variation, source of nutritional status bone brain liver toxicology
The following articles in journals at HighWire Press have cited this article:
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R. A. Yokel, S. S. Rhineheimer, P. Sharma, D. Elmore, and P. J. McNamara Entry, Half-Life, and Desferrioxamine-Accelerated Clearance of Brain Aluminum after a Single 26Al Exposure Toxicol. Sci., November 1, 2001; 64(1): 77 - 82. [Abstract] [Full Text] [PDF] |
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