Uptake of bixin by blood lipoproteins and leukocytes in cats

Bixin was used originally as remedies for asthma, pleurisy, sunstroke and burns. The uptake of bixin in companion animals is unknown. We fed domestic shorthair cats bixin extracted from the annatto seed (1.6% bixin, <0.3% norbixin). In experiment 1, domestic cats (3 yr old; n = 8/dose) were orall...

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Bibliographic Details
Published in:The FASEB journal Vol. 21; no. 5; p. A353
Main Authors: Park, Jean Soon, Hayek, Michael G., Ceddia, Michael A., Reinhart, Gregory G., Chew, Boon P.
Format: Journal Article
Language:English
Published: Federation of American Societies for Experimental Biology 01-04-2007
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Summary:Bixin was used originally as remedies for asthma, pleurisy, sunstroke and burns. The uptake of bixin in companion animals is unknown. We fed domestic shorthair cats bixin extracted from the annatto seed (1.6% bixin, <0.3% norbixin). In experiment 1, domestic cats (3 yr old; n = 8/dose) were orally dosed with 0, 1, 5 or 10 mg bixin and blood was taken at 0, 1, 2, 4 and 8 h after feeding. Plasma bixin concentrations in cats fed 0, 1, 5 or 10 mg bixin increased dose‐dependently and reached maximum concentrations of 0, 9, 45 and 119 nmol/L, respectively. Peak bixin concentration was observed at 1 h after dosing, with an elimination half‐life of 2 h. The uptake profile for norbixin was similar to bixin except that norbixin concentration averaged 10–30 times lower than bixin. In experiment 2, cats were orally administered 0, 1, 5 or 10 mg bixin daily for 14 d. Blood was taken 1 h after dosing on d 0, 1, 3, 6, 9, and 14 to measure bixin uptake in plasma, lipoproteins (d 6 and 14) and leukocyte subcellular fractions (d 14). Plasma bixin concentration in cats fed bixin peaked on d 1. Bixin uptake by HDL, LDL and VLDL was two times higher on d 14 compared to d 6. Uptake by the HDL and LDL fractions was similar and was approximately 2 times higher than in the VLDL fraction. The steady‐state plasma concentration was 0, 10, 48 and 106 nmol/L, respectively. There was a significant dose‐dependent uptake of bixin by leukocyte nuclei, microsomes and mitochondria. At the 5 and 10 mg doses, the mitochondria accounted for 58–60% of total bixin uptake by blood leukocytes; distribution between the nuclei and microsomes was similar.
ISSN:0892-6638
1530-6860
DOI:10.1096/fasebj.21.5.A353