Abstract

Lycopene has been shown to have various biologic effects, and rats and mice are often used for elucidating its in vivo effects and mechanisms. Here, we compared plasma and tissue lycopene levels in F344 rats, BALB/c mice, nude mice, and gerbils by oral supplementation with lycopene (20 mg/kg BW x 2d) every other morning for 10 days. We found that livers accumulated substantially more lycopene than kidneys and that the hepatic lycopene contents varied greatly in these animals, with gerbils being most efficient (1432 +/- 235 nmol/g), followed by nude mice (524 +/- 133 nmol/g), F344 rats (28 +/- 11 nmol/g), and BALB/c mice (5 +/- 2 nmol/g). Plasma lycopene concentrations also varied greatly, of which the highest was found in gerbils (667 +/- 160 nmol/L), followed by nude mice (224 +/- 51 nmol/L), then by BALB/c mice and F344 rats (198 +/- 52 and 139 +/- 41 nmol/L, respectively). Interestingly, plasma and tissue beta-carotene concentrations in these animals were markedly decreased by lycopene supplementation. To determine the steady-state levels of plasma lycopene, we fed 10 gerbils with lycopene (20 mg/kg BW x 2d) for 20 days, and we found a steady-state level of plasma lycopene between 597 to 722 nmol/L. Our results demonstrate that gerbils and nude mice are better accumulators than F344 rats and BALB/c mice, and that the former species may be more useful for studying the in vivo effects of lycopene.

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.