bioRxivPharmacology & Toxicology
Safety and uptake of fully oxidized β-carotene
G. W. Burton, T. J. Mogg, J. Stupak, F. C. Stark, S. M. Twine, J. Li
Abstract
Spontaneous oxidation of {beta}-carotene yields a polymer-rich product (OxBC) also containing small amounts of many apocarotenoids. OxBC extends {beta}-carotenes benefits beyond vitamin A, finding utility in supporting health in livestock, pets, and humans. Although naturally occurring OxBC is consumed in foods and feeds, a direct demonstration here of safety of synthetic OxBC supports its increasing usage. A toxicological study in rats showed a maximum tolerated single oral dose, an LD50, and a NOAEL of 5,000, 30,079 and 1875 mg/kg body weight, respectively. The repeat-dose 90-day oral toxicity study showed no adverse physiological or pathological effects. A first study of OxBC uptake by mice over 2-5 days into a select set of tissues showed OxBC already was naturally present. The highest levels were in liver, lung, and hamstring. Despite dosing, no net increases occurred in liver, kidney, lung, and muscle. Net increases occurred in urine, intestinal content, plasma, feces, spleen, and cecum, consistent with processing of OxBC and preferential elimination of polymer. Compared to the 4:1 polymer: apocarotenoid ratio of OxBC, polymer was enriched in liver and spleen and depleted in lung, kidney, hamstring, and abdominal muscle. The apparent control of OxBC in major tissues further supports its safety.
- organism: rat
- organism: mouse
- research focus: drug response / drug discovery
- research focus: synaptic & neural circuits
- approach: experimental assay
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