Rye is among the cereals with highest content of dietary fibre. A high rye food intake has been associated with improved metabolic risk factors in some but not all observational...
This study aimed to elucidate the impacts of carrier
oil types
(long chain triglycerides (LCT), medium chain triglycerides (MCT),
and orange oil (indigestible oil)) on the micellization and cellular
uptake of β-carotene (BC) formulated in O/W emulsions, with
an emphasis on the role of intestinal transporters. The micellization
and cellular uptake of BC in the gastrointestinal tract were evaluated
via an in vitro digestion model and a Caco-2 cell
monolayer. And the interactions between lipids and intestinal transporters
were monitored by nontargeted lipidomics, RT-PCR, and Western blot.
The BC micellization rates followed a decreasing trend in emulsions:
corn oil (69.47 ± 4.19%) > MCT (22.22 ± 0.89%) > orange
oil (11.01 ± 2.86%), whereas the cellular uptake rate of BC was
significantly higher in MCT emulsion (56.30 ± 20.13%) than in
corn oil emulsion (14.01 ± 1.04%, p < 0.05).
The knockdown of SR-B1 led to a 31.63% loss of BC
cellular uptake from MCT micelles but had no effect on corn oil micelles.
Lipidomics and transporter analysis revealed that TG (10:0/10:0/12:0)
and TG (10:0/12:0/12:0) might be the fingerprint lipids that promoted
the cellular absorption of BC-MCT micelles via stimulating the mRNA
expression of SR-B1.
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