期刊
FOOD AND CHEMICAL TOXICOLOGY
卷 46, 期 12, 页码 3659-3663出版社
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.fct.2008.09.041
关键词
Accelerator mass spectrometry; Aluminum; Atomic absorption spectrometry; Oral bioavailability; Rat; Tea beverage
资金
- NIH [R01 E511305]
- NATIONAL INSTITUTE OF ENVIRONMENTAL HEALTH SCIENCES [R01ES011305] Funding Source: NIH RePORTER
The objective was to estimate Oral Al bioavailability from tea infusion in the rat, using the tracer (26)Al. (26)Al citrate was injected into tea leaves. An infusion was prepared from the dried leaves and given intra-gastrically to rats which received concurrent intravenous (27)Al infusion. Oral Al bioavailability (F) was calculated from the area under the (26)Al, compared to (27)Al serum concentration x time curves. Bioavailability from tea averaged 0.37%; not significantly different from water (F = 0.3%), or basic sodium aluminum phosphate (SALP) in cheese (F = 0.1-0.3%), but greater than acidic SALP in a biscuit (F = 0.1%). Time to maximum serum (26)Al concentration was 1.25, 1.5, 8 and 4.8 h, respectively. These results of oral Al bio-availability x daily consumption by the human suggest tea can provide a significant amount of the Al that reaches systemic circulation. This can allow distribution to its target organs of toxicity, the central nervous, skeletal and hematopoietic systems. Further testing of the hypothesis that Al contributes to Alzheimer's disease may be more warranted with studies focusing on total average daily food intake, including tea and other foods containing appreciable Al, than drinking water. (C) 2008 Elsevier Ltd. All rights reserved.
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