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1.
Food Chem ; 287: 167-175, 2019 Jul 30.
Artículo en Inglés | MEDLINE | ID: mdl-30857686

RESUMEN

Bakery products with fruit fillings are growing fast. Blueberry-filled pastries are widely consumed in China. This study aimed to investigate the effects of two thermal processing procedures (stir-frying and baking) on flavonoid profile, antioxidant property, and hydroxymethylfurfural (HMF) formation during preparation of blueberry-filled pastries. Stir-frying contributed the most to the variations in these values in blueberry filling. Anthocyanins (48%-53% reduction in total) were more susceptible to thermal processing than flavonols (11%-16%). Among anthocyanins, delphinidin glycosides (61%-67% reduction) were the most unstable, followed by malvidin (52%-58%), petunidin (40%-45%), and cyanidin (38%-41%). A high level of HMF (300 mg/kg) was formed during stir-frying. Except for anthocyanins, baking did not significantly influence HMF formation, flavonol degradation, and antioxidant property in the fillings. Stir-frying processing conditions rather than baking must be further investigated for nutrient retention and HMF inhibition.


Asunto(s)
Antioxidantes/análisis , Arándanos Azules (Planta) , Culinaria/métodos , Flavonoides/análisis , Frutas/química , Furaldehído/análogos & derivados , Antocianinas/análisis , China , Furaldehído/síntesis química , Glicósidos/análisis , Calor
2.
Food Res Int ; 122: 443-449, 2019 08.
Artículo en Inglés | MEDLINE | ID: mdl-31229098

RESUMEN

Various Maillard reaction systems were established to investigate the effect of maize bran feruloylated oligosaccharides (FOs) on the formation of both endogenous and exogenous advanced glycation end-products (AGEs) under different pH values. The formation of AGEs and four kinds of dicarbonyl compounds (glyoxal, methylglyoxal, 3-deoxyglucosulose, 2,3-butanedione) were determined by fluorescence spectrophotometry and HPLC, respectively. Results showed that maize bran FOs effectively inhibited the production of fluorescent AGEs. Moreover, increase in pH, temperature and concentration of FOs in reaction systems elevated the inhibition effects of feruloylated oligosaccharides, fluorescent AGEs and dicarbonyl compounds. Mainly because of the ester bond of FOs at high pH and/or temperature systems are readily to be hydrolyzed, resulting in the release of ferulic acid.


Asunto(s)
Aminoácidos/metabolismo , Fibras de la Dieta/análisis , Glucosa/metabolismo , Productos Finales de Glicación Avanzada/metabolismo , Oligosacáridos/análisis , Albúmina Sérica Bovina/metabolismo , Zea mays/química , Ácidos Cumáricos/metabolismo , Diacetil/metabolismo , Productos Finales de Glicación Avanzada/antagonistas & inhibidores , Glioxal/metabolismo , Concentración de Iones de Hidrógeno , Hidrólisis , Oligosacáridos/farmacología , Piruvaldehído/metabolismo , Temperatura
3.
Biomed Pharmacother ; 100: 15-19, 2018 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-29421577

RESUMEN

Ischemia/reperfusion (I/R) injury is a main cause of acute myocardial infarction, and the pathogenesis of I/R injury is still not definitely confirmed. In the present study, we aimed to explore the roles of miR-204 in hypoxia/reoxygenation (H/R)-induced cardiomyocyte injury in vitro. The H9C2 cells were subjected to hypoxia for 12 h followed by reoxygenation for another 24 h, and we found that miR-204 was significantly down-regulated after H/R treatment. Transfection of miR-204 mimics attenuated the H/R-induced impaired cell viability and increased apoptosis rates. Furthermore, SIRT1 was identified as a direct target of miR-204, and its expression is negatively regulated by miR-204. Forced expression of SIRT1 could partly rescue the effects of miR-204 on H/R-induced apoptosis and autophagy. Taken together, our study first revealed that overexpression of miR-204 has a protective effect against myocardial I/R injury.


Asunto(s)
Autofagia/genética , MicroARNs/genética , Miocitos Cardíacos/patología , Oxígeno/metabolismo , Sirtuina 1/metabolismo , Animales , Hipoxia de la Célula/genética , Línea Celular , Regulación de la Expresión Génica , Daño por Reperfusión Miocárdica/genética , Daño por Reperfusión Miocárdica/metabolismo , Daño por Reperfusión Miocárdica/patología , Miocitos Cardíacos/metabolismo , Ratas , Transducción de Señal
4.
Biomed Pharmacother ; 104: 712-717, 2018 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-29807220

RESUMEN

Myocardial ischemic/reperfusion (I/R) injury often leads to irreversible myocardial cell death and even heart failure, with limited therapeutic possibilities. In the present study, we evaluated the protective effects of shikonin (SHK) against hypoxia/reoxygenation (H/R)-induced cardiomyocyte damage and explored the underlying mechanisms. H9C2 cardiomyocytes were pretreated with different doses of SHK prior to H/R exposure. We observed that SHK pretreatment significantly increased cell viability, attenuated LDH release, and suppressed cardiomyocyte apoptosis induced by H/R exposure. SHK pretreatment also restored the loss of mitochondrial membrane potential (MMP) and cytochrome c release. In addition, SHK significantly enhanced the phosphorylation of Akt and GSK-3ß in H/R-treated H9C2 cells. These protective effects of SHK were partially reversed by LY294002, a specific PI3K/Akt inhibitor. Therefore, our findings suggested that SHK might be a promising agent for myocardial I/R injury, and PI3K/Akt signaling plays a crucial role during this process.


Asunto(s)
Hipoxia/metabolismo , Daño por Reperfusión Miocárdica/tratamiento farmacológico , Miocitos Cardíacos/efectos de los fármacos , Naftoquinonas/farmacología , Fosfatidilinositol 3-Quinasas/metabolismo , Sustancias Protectoras/farmacología , Proteínas Proto-Oncogénicas c-akt/metabolismo , Animales , Apoptosis/efectos de los fármacos , Cardiotónicos/farmacología , Línea Celular , Supervivencia Celular/efectos de los fármacos , Cromonas/farmacología , Glucógeno Sintasa Quinasa 3 beta/metabolismo , Potencial de la Membrana Mitocondrial/efectos de los fármacos , Mitocondrias/efectos de los fármacos , Mitocondrias/metabolismo , Morfolinas/farmacología , Daño por Reperfusión Miocárdica/metabolismo , Miocardio/metabolismo , Miocitos Cardíacos/metabolismo , Fosforilación/efectos de los fármacos , Ratas , Transducción de Señal/efectos de los fármacos
5.
J Agric Food Chem ; 66(43): 11451-11458, 2018 Oct 31.
Artículo en Inglés | MEDLINE | ID: mdl-30303013

RESUMEN

The absorption of a 5-hydroxymethylfurfural (HMF)-cysteine adduct, 1-dicysteinethioacetal-5-hydroxymethylfurfural (DCH), and its effect on antioxidant activity and gut microbiota were investigated. Results indicated that DCH is more easily absorbed in rats than HMF. Serum DCH concentrations were 15-38-fold of HMF concentrations from 30 to 180 min after intragastrical administration at the level of 100 mg/kg of body weight, and 2.7-4.5% of absorbed DCH was converted to HMF. The malondialdehyde content in the plasma, heart, liver, and kidneys significantly increased after drug (100 mg/kg of bw) administration for 1 week, suggesting that HMF and DCH were oxidative-stress-inducing agents, instead of antioxidant agents, in rats. HMF and DCH also modulated gut microbiota. HMF promoted the growth of Lactobacillus, Tyzzerella, Enterobacter, and Streptococcus. DCH increased the ratio of Firmicutes/ Bacteroidetes and promoted the growth of Akkermansia, Shigella, and Escherichia while inhibiting the growth of Lactobacillus.


Asunto(s)
Cisteína/farmacocinética , Furaldehído/análogos & derivados , Microbioma Gastrointestinal/efectos de los fármacos , Estrés Oxidativo , Animales , Antioxidantes/metabolismo , Furaldehído/farmacocinética , Masculino , Malondialdehído/metabolismo , Ratas Sprague-Dawley
6.
J Nutr Sci Vitaminol (Tokyo) ; 63(1): 69-80, 2017.
Artículo en Inglés | MEDLINE | ID: mdl-28367928

RESUMEN

Winged beans are an important natural source of some micronutrients. This paper presents the first complete characterization of folate derivatives including polyglutamyl 5-methyltetrahydrofolate (5-CH3-H4PteGlun), folate species and total folate accumulating in pods and immature seeds of winged beans from 9 cultivars and 7 growth stages. 5-CH3-H4PteGlun and folate species were determined with a UHPLC-MS/MS method. Accurate determination of 5-CH3-H4PteGlun and folate species was optimized and validated according to EMA guidelines including method selectivity, sensitivity, linearity, accuracy, precision, matrix effect and carry-over. The level of total folate is in the range of 73-200 µg/100 g in the pods and 33-61 µg/100 g in the immature seeds. The predominant folate species in winged beans is 5-CH3-H4PteGlu1. 5-CH3-H4PteGlu5 is the major polyglutamyl folate derivative. The level of total folate is increased about 4 fold with advancing maturity. For pods, the chain length is increased with growth which shifts from 5-CH3-H4PteGlu1 in the early stage to 5-CH3-H4PteGlu5 and 5-CH3-H4PteGlu6 in the 7th stage. Our findings demonstrate that winged beans are good source of folate. The validated UHPLC-MS/MS method allows for the determination of 5-CH3-H4PteGlun and folate species from other vegetable matrices.


Asunto(s)
Cromatografía Líquida de Alta Presión , Ácido Fólico/análisis , Phaseolus/química , Semillas/química , Espectrometría de Masas en Tándem , Tetrahidrofolatos/análisis , Semillas/crecimiento & desarrollo , Especificidad de la Especie , Verduras/química
7.
J Agric Food Chem ; 63(47): 10257-62, 2015 Dec 02.
Artículo en Inglés | MEDLINE | ID: mdl-26554667

RESUMEN

Seven new phloroglucinol derivatives (1-7) were isolated from the fruit tree Syzygium jambos together with four known triterpenoids (8-11) and two known flavones (12 and 13). According to the spectroscopic analyses (infrared, electrospray ionization mass spectrometry (ESIMS), high-resolution ESIMS, 1D and 2D nuclear magnetic resonance), the structures of compounds 1-7 were elucidated as jambone A (1), jambone B (2), jambone C (3), jambone D (4), jambone E (5), jambone F (6), and jambone G (7). All the isolates were determined for their cytotoxic activities on melanoma cells by 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide assay, and compounds 10 and 11 showed potent activities. Moreover, compounds 1, 2, 4-7, 12, and 13 exhibited weak antioxidant activities under ferric-reducing antioxidant power and 2,2-diphenyl-1-picryhydrazyl radical-scavenging assays.


Asunto(s)
Floroglucinol/química , Extractos Vegetales/química , Syzygium/química , Frutas/química , Estructura Molecular , Floroglucinol/toxicidad , Extractos Vegetales/toxicidad
8.
Nat Prod Commun ; 9(1): 13-4, 2014 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-24660450

RESUMEN

One new and seven known diterpenoids were isolated from the aerial parts of Andrographis paniculata, and their structures elucidated on the basis of spectroscopic and spectrometric analysis, as well as chemical methods. The in vitro antiviral activities of these compounds against respiratory syncytial virus (RSV) were assayed.


Asunto(s)
Andrographis/química , Diterpenos/aislamiento & purificación , Antivirales/análisis , Diterpenos/química , Estructura Molecular , Componentes Aéreos de las Plantas/química , Plantas Medicinales/química
9.
J Hazard Mater ; 268: 1-5, 2014 Mar 15.
Artículo en Inglés | MEDLINE | ID: mdl-24462985

RESUMEN

This research was aimed to investigate why chlorogenic acid, presents at high concentrations in some food raw material, influences acrylamide formation. In the asparagine/glucose Maillard reaction system (pH=6.8), addition of chlorogenic acid significantly increased acrylamide formation and inhibited its elimination. In contrast, the quinone derivative of chlorogenic acid decreased acrylamide formation. Three mechanisms may be involved for increasing acrylamide formation by chlorogenic acid. Firstly, it increased the formation of HMF, which acts as a more efficient precursor than glucose to form acrylamide. Secondly, it decreased activation energy for conversion of 3-aminopropionamide (3-APA) to acrylamide (from 173.2 to 136.6kJ/mol), and enhances deamination from 3-APA. And thirdly, it prevented attack of the produced acrylamide from free radicals by keeping high redox potential during the Maillard reaction.


Asunto(s)
Acrilamida/química , Ácido Clorogénico/química , Flavonas/química , Contaminación de Alimentos , Modelos Químicos , beta-Alanina/análogos & derivados , Acrilamida/análisis , Desaminación , Reacción de Maillard , Oxidación-Reducción , Quinonas/química , beta-Alanina/química
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