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Furthermore, GSH content in bone marrow may predict this tissue's sensitivity to cytotoxic agents.
Our results indicate that the accumulated aluminium content in bone during life does not substantially influence the extent of osteoporosis.
Furthermore, there were no differences in adjusted mean BMD or BMC values between tertiles of aluminium content in bone.
No associations were found between the aluminium content in bone and femoral-neck width or area (Table 2).
DNA cell cycle distribution and glutathione (GSH) content in bone marrow were measured both at daytime and midnight over single 24 h periods in 15 cancer patients.
No significant association between the aluminium content in bone and femoral neck BMD, BMC or width could be found after multivariate adjustment.
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The most commonly used approach for evaluating bioavailability, and a comprehensive one, is based on monitoring BLLs over the course of the experiment for different dosages, as well as the Pb content in bones, kidneys, and liver at the end of the exposure period for different dosages.
Low Mg content in bones has been repeatedly reported in diabetic rats where it was reversible through the administration of Mg [ 33] and insulin [ 34].
Moreover, Boyar [ 74] showed that an excess of Se increased the amount of carbonate content in bones of rats injected intraperitoneally with 5 μmol Na2SeO3/kg for 4 weeks.
This data may suggest that lowering the calcium content in bones is due to its escape into blood or a remodelling of the hydroxyapatite structure under the influence of the electromagnetic field.
The results of Boyar [ 34] showed that an excess of Se increased the amount of carbonate content in bones of Wistar rats injected intraperitoneally with 5 μmol Na2SeO3/kg for 4 weeks.
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