Does the activity of chromium in "slimming agents" stem from the formation of cancer-causing substances?
It is undisputed that special complexes of chromium(III) demonstrate an insulin-intensifying effect. They are therefore under consideration as potential drugs for diabetes (apart from their widespread use in dietary supplements), even though the mechanism of their effect is not known. In a project funded by the Australian Research Council, Peter Lay, Irma Mulyani, and Aviva Levina have now developed a novel explanation. First, they throw out the current notion that chromium(III) cannot be converted into chromium(VI) in the body. In immune reactions, for example, the human body releases very strong oxidizing agents, such as hydrogen peroxide, which were demonstrated to oxidize chromium(III), even under physiological conditions. "It is postulated that it is the resulting chromium(VI) and chromium(V) species that then interfere with our metabolism," explains Lay.
When insulin is released by the pancreas, it docks onto a receptor on the surface of cells. Afterwards, a phosphate group attaches onto the receptor, which releases a signal cascade that orders the cell to take up glucose from the blood. When the insulin is gone, an enzyme, tyrosine phosphatase, splits the phosphate groups off the receptor, returning the cell to its original state. This is where, according to the Australian researchers, the chromium(V) or chromium(VI) species step in: they inhibit the tyrosine phosphatase, intensifying the effect of the insulin. Chromium(III) species, in contrast, are not tyrosine phosphatase inhibitors.
The trouble is that chromium(VI) has long been established as a human carcinogen, as highlighted in the film Erin Brokovitch. "In light of our new findings," stresses Lay, "the safety of chromium(III) compounds as nutritional supplements or drugs should be re-examined very carefully, particularly for heavy users of the supplements, such as elite athletes."
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