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1.
Food Chem ; 373(Pt B): 131496, 2022 Mar 30.
Artículo en Inglés | MEDLINE | ID: mdl-34836668

RESUMEN

The application of blueberry anthocyanins (ANs) was limited due to their low in-process stability and bioavailability. In our study, the stability and antioxidant capacity of ANs before and after adding bovine serum albumin (BSA) were examined by simulating various processing, storage (light, sucrose, and vitamin C (Vc)), and in vitro simulated digestion parameters. For this purpose, pH-differential method, high performance liquid chromatography-tandem mass spectrometry (HPLC-MS/MS), peroxyl scavenging capacity assay, and cellular antioxidant assay were conducted. BSA at different concentrations, specifically at 0.15 mg/mL, inhibited the degradation of ANs and the loss of antioxidant capacity. The results suggest that BSA has a positive effect on ANs.


Asunto(s)
Arándanos Azules (Planta) , Antocianinas/análisis , Antioxidantes , Cromatografía Líquida de Alta Presión , Digestión , Extractos Vegetales , Albúmina Sérica Bovina , Espectrometría de Masas en Tándem
2.
Food Chem ; 334: 127526, 2021 Jan 01.
Artículo en Inglés | MEDLINE | ID: mdl-32702589

RESUMEN

Blueberry anthocyanins are well-known for their diverse biological functions. However, the instability during digestion results in their weak bioavailability. The current study aimed to investigate the alteration in the stability, antioxidant capacity and bioaccessibility of blueberry anthocyanins with the addition of α-casein and ß-casein in a simulated digestion system using pH differential method, HPLC-MS analysis, peroxyl scavenging capacity (PSC) assay, cellular antioxidant activity (CAA) and penetration test. The results showed that both α-casein and ß-casein could increase the stability of blueberry anthocyanins during intestinal digestion and protect their antioxidant capacity. Moreover, the addition of α-casein or ß-casein would enhance the bioaccessibility of blueberry anthocyanins. In conclusion, our study highlights that the interaction between α-casein or ß-casein with blueberry anthocyanins can protect the compounds against influences associated with the simulated digestion.


Asunto(s)
Antocianinas/química , Antioxidantes/química , Arándanos Azules (Planta)/química , Caseínas/química , Antocianinas/metabolismo , Antocianinas/farmacología , Arándanos Azules (Planta)/metabolismo , Caseínas/metabolismo , Supervivencia Celular/efectos de los fármacos , Cromatografía Líquida de Alta Presión , Digestión , Frutas/química , Frutas/metabolismo , Células Hep G2 , Humanos , Concentración de Iones de Hidrógeno , Espectrometría de Masas , Extractos Vegetales/química , Estabilidad Proteica
3.
J Nutr Biochem ; 64: 88-100, 2019 02.
Artículo en Inglés | MEDLINE | ID: mdl-30471564

RESUMEN

Polyphenols are known for their various health benefits. Blueberries are dietary sources of polyphenols with reported health benefits. However, the role of blueberry polyphenols in alleviating obesity is not completely understood. This study investigated the potential positive effect of blueberry polyphenol extract (PPE) on high-fat diet (HFD)-induced obesity in C57BL/6 J mice by modulation of the gut microbiota. Four-week-old C57BL/6 J mice were fed a normal-fat diet or HFD with or without PPE or Orlistat for 12 weeks. Mice fed HFD exhibited increased body weight and adipose tissue weight and disordered lipid metabolism. In contrast, PPE inhibited body weight gain and returned lipid metabolism to normal. Furthermore, 16S rRNA gene sequencing of the fecal microbiota suggested that PPE changed the composition of the gut microbiota in C57BL/6 J mice and modulated specific bacteria such as Proteobacteria, Deferribacteres, Actinobacteria, Bifidobacterium, Desulfovibrio, Adlercreutzia, Helicobacter, Flexispira, and Prevotella. Orlistat also improved obesity and metabolic alterations of HFD mice and modulated the composition of the gut microbiota. Our findings suggest that PPE, as a potential prebiotic agent, influences the gut microbiota to positively affect HFD-induced obesity in C57BL/6 J mice.


Asunto(s)
Fármacos Antiobesidad/farmacología , Arándanos Azules (Planta)/química , Microbioma Gastrointestinal/efectos de los fármacos , Obesidad/dietoterapia , Polifenoles/farmacología , Prebióticos , Tejido Adiposo Blanco/efectos de los fármacos , Tejido Adiposo Blanco/metabolismo , Animales , Dieta Alta en Grasa/efectos adversos , Microbioma Gastrointestinal/genética , Metabolismo de los Lípidos/efectos de los fármacos , Hígado/efectos de los fármacos , Hígado/metabolismo , Masculino , Ratones Endogámicos C57BL , Obesidad/etiología , Obesidad/microbiología , Extractos Vegetales/química , Extractos Vegetales/farmacología
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