β-carotene genetically-enriched lyophilized orange juice increases antioxidant capacity and reduces β-amyloid proteotoxicity and fat accumulation in Caenorhabditis elegans

• β-carotene content of genetically modified orange was 33-fold higher. • β-carotene-enriched LOJ provided greater antioxidant capacity and stress resistance. • β-carotene-enriched LOJ reduced β-amyloid proteotoxicity. • β-carotene-enriched LOJ showed higher hypolipidemic activity in glucose rich di...

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Veröffentlicht in:Food chemistry. Molecular sciences 2022-12, Vol.5, p.100141-100141, Article 100141
Hauptverfasser: Raquel Ferreira Paulo, Iolanda, Basílio de Oliveira Caland, Ricardo, Orlando Muñoz Cadavid, Cesar, Martins Melo, Giovanna, Soares De Castro Bezerra, Liliane, Pons, Elsa, Peña, Leandro, de Paula Oliveira, Riva
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Sprache:eng
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Zusammenfassung:• β-carotene content of genetically modified orange was 33-fold higher. • β-carotene-enriched LOJ provided greater antioxidant capacity and stress resistance. • β-carotene-enriched LOJ reduced β-amyloid proteotoxicity. • β-carotene-enriched LOJ showed higher hypolipidemic activity in glucose rich diet. Citrus sinensis orange juice is an excellent dietary source of β-carotene, a well-known antioxidant. However, β-carotene concentrations are relatively low in most cultivars. We developed a new orange through metabolic engineering strategy (GS) with 33.72-fold increase in β-carotene content compared to its conventional counterpart (CV). Using Caenorhabditis elegans , we found that animals treated with GS showed a greater reduction in intracellular reactive oxygen species (ROS) which is associated with a greater resistance to oxidative stress and induction of the expression of antioxidant genes. Moreover, animals treated with GS orange showed a more effective protection against β-amyloid proteotoxicity and greater hypolipidemic effect under high glucose diet compared to animals treated with CV. These data demonstrate that the increased amount of β-carotene in orange actually provides a greater beneficial effect in C. elegans and a valuable proof of principle to support further studies in mammals and humans.
ISSN:2666-5662
2666-5662
DOI:10.1016/j.fochms.2022.100141