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1.
Animals (Basel) ; 10(10)2020 Oct 15.
Artículo en Inglés | MEDLINE | ID: mdl-33076543

RESUMEN

This study aimed to investigate the optimal addition of terpene-based Pinus densiflora and Mentha canadensis extracts, with antioxidant and methane reduction effects, as feed supplements to ruminants. Two cannulated steers (450 ± 30 kg), consuming Timothy Hay and a commercial concentrate (60:40, w/w) twice daily (at 09:00 and 17:30) at 2% of body weight, with free access to water and a mineral block, were used as rumen fluid donors. In vitro fermentation experiments, with Timothy Hay as the substrate, were conducted with P. densiflora and M. canadensis extracts as supplements to achieve concentrations of 30, 50, and 70 mg/L on a Timothy Hay basis. Fibrobacter succinogenes decreased in proportion upon P. densiflora and M. canadensis extract supplementation at 50 mg/L, while the dry matter degradability of the feed was not significantly different (p < 0.05). Methane emission was significantly lower in the 50 and 70 mg/L treatment groups, for both extracts, at 12 h (p < 0.05). Based on methane production and antioxidant activity, our study suggests that 30 mg/L addition is the most appropriate level of supplementation.

2.
Pharm Biol ; 53(9): 1260-6, 2015.
Artículo en Inglés | MEDLINE | ID: mdl-25853960

RESUMEN

CONTEXT: Alzheimer's disease (AD) is a neurodegenerative disorder characterized by the abnormal accumulation of ß-amyloid (Aß). Multiple Aß-aggregated species have been identified, and neurotoxicity appears to be correlated with the amount of non-fibrillar oligomers. Potent inhibitors of Aß oligomer formation or Aß-induced cell toxicity have emerged as attractive means of therapeutic intervention. Eremochloa ophiuroide Hack. (Poaceae), also known as centipedegrass (CG), originates from China and South America and is reported to contain several C-glycosyl flavones and phenolic constituents. OBJECTIVE: We investigated whether CG could suppress Aß aggregation, BACE1 activity, and toxicity at neuronal cell. MATERIALS AND METHODS: The inhibitory effect of CG extracts toward aggregation of Aß42 was investigated in the absence and presence of 50 µg/mL CG. We investigated the inhibitory effects of CG (0-5 µg/mL) on BACE1 using fluorescence resonance energy transfer (FRET)-based assay. The effects of CG (0-75 µg/mL) on Aß42-induced neurotoxicity were examined in PC12 cells in the presence or absence of maysin and its derivatives of CG. RESULTS: We isolated EA-CG fraction (70% MeOH fraction from EtOAc extracts) from methanol extracts of CG, which contained approximately 60% maysin and its derivatives. In the present studies, we found that several Aß oligomeric forms such as the monomer, dimer, trimer, and highly aggregated oligomeric forms were remarkably inhibited in the presence of 50 µg/mL of EA-CG. EA-CG also inhibited BACE1 enzyme activity in a dose-dependent manner. EA-CG treatment generated approximately 50% or 85% inhibition to the control at the tested concentrations of 1 or 5 µg/mL, respectively. Moreover, the neurotoxicity induced by Aß42 was significantly reduced by treatment of EA-CG, and the 75 µg/mL EA-CG treatment significantly increased cell viability up to 82.5%. DISCUSSION AND CONCLUSION: These results suggested that the anti-Alzheimer's effects of CG occurred through inhibition of neuronal cell death by intervening with oligomeric Aß formation and reducing BACE1 activity. Maysin in CG could be an excellent therapeutic candidate for the prevention of AD.


Asunto(s)
Secretasas de la Proteína Precursora del Amiloide/antagonistas & inhibidores , Péptidos beta-Amiloides/metabolismo , Ácido Aspártico Endopeptidasas/antagonistas & inhibidores , Inhibidores Enzimáticos/farmacología , Neuronas/efectos de los fármacos , Fármacos Neuroprotectores/farmacología , Fragmentos de Péptidos/metabolismo , Extractos Vegetales/farmacología , Poaceae , Secretasas de la Proteína Precursora del Amiloide/metabolismo , Animales , Ácido Aspártico Endopeptidasas/metabolismo , Muerte Celular/efectos de los fármacos , Citoprotección , Relación Dosis-Respuesta a Droga , Inhibidores Enzimáticos/aislamiento & purificación , Flavonoides/farmacología , Transferencia Resonante de Energía de Fluorescencia , Glucósidos/farmacología , Humanos , Neuronas/metabolismo , Neuronas/patología , Fármacos Neuroprotectores/aislamiento & purificación , Células PC12 , Fitoterapia , Extractos Vegetales/aislamiento & purificación , Plantas Medicinales , Poaceae/química , Agregación Patológica de Proteínas , Ratas
3.
Nutrients ; 6(6): 2179-95, 2014 Jun 05.
Artículo en Inglés | MEDLINE | ID: mdl-24905748

RESUMEN

The aim of the current study is to examine the improving effect of Sasa borealis stem (SBS) extract extracts on high-fat diet (HFD)-induced hepatic steatosis in rats. To determine the hepatoprotective effect of SBS, we fed rats a normal regular diet (ND), HFD, and HFD supplemented with 150 mg/kg body weight (BW) SBS extracts for five weeks. We found that the body weight and liver weight of rats in the HFD + SBS group were significantly lower than those in the HFD group. Significantly lower serum total cholesterol (TC) and triglyceride (TG) concentrations were observed in the SBS-supplemented group compared with the HFD group. We also found that the HFD supplemented with SBS group showed dramatically reduced hepatic lipid accumulation compared to the HFD alone group, and administration of SBS resulted in dramatic suppression of TG, TC in the HFD-induced fatty liver. In liver gene expression within the SBS treated group, PPARα was significantly increased and SREBP-1c was significantly suppressed. SBS induced a significant decrease in the hepatic mRNA levels of PPARγ, FAS, ACC1, and DGAT2. In conclusion, SBS improved cholesterol metabolism, decreased lipogenesis, and increased lipid oxidation in HFD-induced hepatic steatosis in rats, implying a potential application in treatment of non-alcoholic fatty liver disease.


Asunto(s)
Grasas de la Dieta/efectos adversos , Hígado Graso/prevención & control , Obesidad/inducido químicamente , Extractos Vegetales/farmacología , Tallos de la Planta/química , Sasa/química , Animales , Antioxidantes/química , Antioxidantes/farmacología , Colesterol/sangre , Grasas de la Dieta/administración & dosificación , Hígado Graso/inducido químicamente , Flavonoides/química , Hígado/efectos de los fármacos , Masculino , Tamaño de los Órganos/efectos de los fármacos , Fenoles/química , Extractos Vegetales/química , Ratas , Ratas Sprague-Dawley , Triglicéridos/sangre
4.
Nutrients ; 6(4): 1737-51, 2014 Apr 24.
Artículo en Inglés | MEDLINE | ID: mdl-24763116

RESUMEN

Drynariae rhizoma has been used to prevent bone loss that occurs with increasing age. However, the chemical compounds in extracts that act on bone metabolism in herbal medicine are poorly understood. This study aimed to investigate and compare the extraction efficacy of polyphenolic compounds, antioxidant activity, and in vitro anti-osteoporosis properties of water extract (DR-DW) and ethanol extract (DR-EtOH) from D. rhizoma. Total phenolics and flavonoids were better extracted with 70% EtOH, and this extraction method also resulted in higher antioxidant activity and in vitro anti-osteoporosis properties in these extracts. In particular, the contents of phloroglucinol, protocatechuic acid ethyl ester, 2-amino-3,4-dimethyl-benzoic acid, 3-(3,5-dimethyl-pyrazol-1-yl)-benzoic acid, chlorogenic acid, syringic acid, trans-ferulic acid, (-)-epigallocatechin, epigallocatechin gallate, quercetin dehydrate, luteolin and emodin in DR-EtOH were higher than those in DR-DW. These results indicated that DR-EtOH could be a good source of natural herbs with anti-osteoporosis properties.


Asunto(s)
Osteoporosis/tratamiento farmacológico , Extractos Vegetales/farmacología , Polypodiaceae/química , Animales , Antioxidantes/análisis , Antioxidantes/farmacología , Catequina/análogos & derivados , Catequina/análisis , Catequina/farmacología , Proliferación Celular/efectos de los fármacos , Células Cultivadas , Ácido Clorogénico/análisis , Ácido Clorogénico/farmacología , Cromatografía Líquida de Alta Presión , Ácidos Cumáricos/análisis , Ácidos Cumáricos/farmacología , Emodina/análisis , Emodina/farmacología , Hidroxibenzoatos/análisis , Hidroxibenzoatos/farmacología , Luteolina/análisis , Luteolina/farmacología , Ratones , Floroglucinol/análisis , Floroglucinol/farmacología , Plantas Medicinales/química , Quercetina/análisis , Quercetina/farmacología , República de Corea
5.
J Med Food ; 17(1): 103-10, 2014 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-24456360

RESUMEN

Schisandra chinensis (SC), a traditional herbal medicine, has been prescribed for patients suffering from various liver diseases, including hepatic cancer, hypercholesterolemia, and CCl4-induced liver injury. We investigated whether SC extract has a protective effect on alcohol-induced fatty liver and studied its underlying mechanisms. Rats were fed with ethanol by intragastric administration every day for 5 weeks to induce alcoholic fatty liver. Ethanol treatment resulted in a significant increase in alanine aminotransferase, aspartate aminotransferase, and hepatic triglyceride (TG) levels and caused fatty degeneration of liver. Ethanol administration also elevated serum TG and total cholesterol (TC) and decreased high-density lipoprotein (HDL) cholesterol levels. However, after administration of ethanol plus SC extracts, the ethanol-induced elevation in liver TC and TG levels was reversed. Elevation in serum TG was not observed after treatment with SC. Moreover, compared with the ethanol-fed group, the rats administered ethanol along with SC extracts for 5 weeks showed attenuated fatty degeneration and an altered lipid profile with decreased serum TC and TG, and increased HDL cholesterol levels. Chronic ethanol consumption did not affect peroxisome proliferator-activated receptor γ (PPARγ) levels, but it decreased PPARα and phospho-AMP-activated protein kinase (AMPK) levels in the liver. However, SC prevented the ethanol-induced decrease in PPARα expression and induced a significant decrease in sterol regulatory element-binding protein-1 expression and increase in phospho-AMPK expression in rats with alcoholic fatty liver. SC administration resulted in a significant decrease in intracellular lipid accumulation in hepatocytes along with a decrease in serum TG levels, and it reversed fatty liver to normal conditions, as measured by biochemical and histological analyses. Our results indicate that the protective effect of SC is accompanied by a significant increase in phospho-AMPK and PPARα expression in hepatic tissue of alcoholic rats, thereby suggesting that SC has the ability to prevent ethanol-induced fatty liver, possibly through activation of AMPK and PPARα signaling.


Asunto(s)
Hígado Graso Alcohólico/prevención & control , Extractos Vegetales/administración & dosificación , Schisandra/química , Proteínas Quinasas Activadas por AMP/genética , Proteínas Quinasas Activadas por AMP/metabolismo , Animales , Colesterol/metabolismo , Hígado Graso Alcohólico/genética , Hígado Graso Alcohólico/metabolismo , Humanos , Hígado/efectos de los fármacos , Hígado/metabolismo , Masculino , PPAR alfa/metabolismo , PPAR gamma/genética , PPAR gamma/metabolismo , Fitoterapia , Ratas , Ratas Sprague-Dawley , Proteína 1 de Unión a los Elementos Reguladores de Esteroles/genética , Proteína 1 de Unión a los Elementos Reguladores de Esteroles/metabolismo , Triglicéridos/metabolismo
6.
Nutrients ; 5(12): 4894-907, 2013 Nov 28.
Artículo en Inglés | MEDLINE | ID: mdl-24288028

RESUMEN

This study was to evaluate the phenolic content and composition of Carthamus tinctorius L. seed extract (CSE) and to further assess its antioxidant and anti-adipogenic activities using various radical scavenging systems and 3T3-L1 cells. Our results show that the total phenolic and flavonoid contents of CSE were 126.0 ± 2.4 mg GAE/g and 62.2 ± 1.9 mg QE/g, respectively. The major phenolic compounds in CSE was (-)-epigallocatechin (109.62 mg/g), with a 4-hydroxy benzhydrazide derivative and gallocatechin present at 18.28 mg/g and 17.02 mg/g, respectively. CSE exhibited remarkable radical scavenging activities, FRAP (ferric reducing antioxidant power) and reducing power in a dose-dependent manner. Moreover, the oxygen radical absorbance capacity (ORAC) value of CSE (0.1 mg/mL) was 62.9 ± 4.7 µM TE (trolox equivalent)/g. During adipogenesis, CSE significantly inhibited fat accumulation in 3T3-L1 cells compared with control cells. Overall, these results indicate that CSE might be a valuable source of bioactive compounds that impart functional food and natural antioxidant properties.


Asunto(s)
Adipogénesis/efectos de los fármacos , Antioxidantes/farmacología , Carthamus tinctorius/química , Fenoles/química , Extractos Vegetales/química , Células 3T3 , Adipocitos/efectos de los fármacos , Adipocitos/metabolismo , Animales , Antioxidantes/aislamiento & purificación , Catequina/análogos & derivados , Catequina/química , Supervivencia Celular , Cromatografía Líquida de Alta Presión , Calor , Hidrazinas/química , Ratones , Fenoles/farmacología , Extractos Vegetales/farmacología , Semillas/química
7.
PLoS One ; 8(7): e69925, 2013.
Artículo en Inglés | MEDLINE | ID: mdl-23936120

RESUMEN

This study examined the anti-obesity effect and mechanism of action of blueberry peel extracts (BPE) in 3T3-L1 cells and high-fat diet (HFD)-induced obese rats. The levels of lipid accumulation were measured, along with the changes in the expression of genes and proteins associated with adipocyte differentiation in 3T3-L1 cells. Evidenced by Oil-red O staining and triglyceride assay, BPE dose-dependently inhibited lipid accumulation at concentrations of 0, 50, and 200 µg/ml. BPE decreased the expression of the key adipocyte differentiation regulator C/EBPß, as well as the C/EBPα and PPARγ genes, during the differentiation of preadipocytes into adipocytes. Moreover, BPE down-regulated adipocyte-specific genes such as aP2 and FAS compared with control adipocytes. The specific mechanism mediating the effects of BP revealed that insulin-stimulated phosphorylation of Akt was strongly decreased, and its downstream substrate, phospho-GSK3ß, was downregulated by BPE treatment in 3T3-L1 cells. Together, these data indicated that BP exerted anti-adipogenic activity by inhibiting the expression of PPARγ and C/EBPß and the Akt signaling pathway in 3T3-L1 adipocytes. Next, we investigated whether BP extracts attenuated HFD-induced obesity in rats. Oral administration of BPE reduced HFD-induced body weight gain significantly without affecting food intake. The epididymal or perirenal adipose tissue weights were lower in rats on an HFD plus BPE compared with the tissue weights of HFD-induced obese rats. Total cholesterol and triglyceride levels in the rats fed BPE were modestly reduced, and the HDL-cholesterol level was significantly increased in HFD plus BP-fed rats compared with those of HFD-fed rats. Taken together, these results demonstrated an inhibitory effect of BP on adipogenesis through the down-regulation of C/EBPß, C/EBPα, and PPARγ and the reduction of the phospho-Akt adipogenic factor in 3T3-L1 cells. Moreover, BPE reduced body weight gain and inhibited fat accumulation in an HFD-induced animal model of obesity.


Asunto(s)
Adipocitos/efectos de los fármacos , Adipogénesis/efectos de los fármacos , Arándanos Azules (Planta)/química , Frutas/química , Obesidad/tratamiento farmacológico , Preparaciones de Plantas/farmacología , Células 3T3-L1 , Adipocitos/metabolismo , Adipocitos/patología , Adipogénesis/genética , Animales , Peso Corporal/efectos de los fármacos , Proteína alfa Potenciadora de Unión a CCAAT/antagonistas & inhibidores , Proteína alfa Potenciadora de Unión a CCAAT/genética , Proteína alfa Potenciadora de Unión a CCAAT/metabolismo , Proteína beta Potenciadora de Unión a CCAAT/antagonistas & inhibidores , Proteína beta Potenciadora de Unión a CCAAT/genética , Proteína beta Potenciadora de Unión a CCAAT/metabolismo , Diferenciación Celular , Dieta Alta en Grasa , Ingestión de Alimentos/efectos de los fármacos , Regulación de la Expresión Génica , Masculino , Ratones , Obesidad/metabolismo , Obesidad/fisiopatología , PPAR gamma/antagonistas & inhibidores , PPAR gamma/genética , PPAR gamma/metabolismo , Proteínas Proto-Oncogénicas c-akt/antagonistas & inhibidores , Proteínas Proto-Oncogénicas c-akt/genética , Proteínas Proto-Oncogénicas c-akt/metabolismo , Ratas , Ratas Sprague-Dawley , Transducción de Señal
8.
Molecules ; 18(6): 6356-65, 2013 May 29.
Artículo en Inglés | MEDLINE | ID: mdl-23760032

RESUMEN

The aim of this study was to investigate the total phenolic content, total flavonoid contents, antioxidant activity and antimicrobial activity of ethanolic extract from stems (S) and leaves (L) of Impatiens balsamina L. (Balsaminaceae), which were harvested in Korea on March 10, 2011 (S1 and L1), May 14, 2011 (S2 and L2), and July 5, 2011 (S3 and L3), respectively. Our results revealed that the total phenolic (79.55-103.94 mg CE/g extract) and flavonoid (57.43-104.28 mg QE/g extract) contents of leaf extract were higher (p < 0.01) than those of stem extract. Leaf extracts (L1, L2, and L3) exhibited stronger (p < 0.01) free radical scavenging activity (66.06, 63.71, and 72.19%, respectively) than that of the positive control. In terms of antimicrobial activity, leaf extracts showed higher inhibitory effects against microorganisms than those of stem extracts (S1, S2, and S3). Among the leaf extracts at different harvest times, L3 showed the greatest antimicrobial activity against both Gram negative and Gram positive strains. From these results, the leaf extract from I. balsamina L. might be a valuable bioactive resource, and would seem to be applicable as a natural antioxidant in food preservation.


Asunto(s)
Antiinfecciosos/farmacología , Antioxidantes/farmacología , Impatiens/química , Extractos Vegetales/química , Hojas de la Planta/química , Tallos de la Planta/química , Antiinfecciosos/química , Antioxidantes/química , Etanol , Flavonoides/química , Flavonoides/farmacología , Depuradores de Radicales Libres/química , Depuradores de Radicales Libres/farmacología , Radicales Libres/antagonistas & inhibidores , Pruebas de Sensibilidad Microbiana , Fenoles/química , Fenoles/farmacología , Estaciones del Año
9.
Curr Drug Targets ; 14(9): 999-1005, 2013 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-23574281

RESUMEN

Carotenoids are considered to act as antioxidants and protect humans from serious disorders such as skin degeneration and ageing, cardiovascular disease, certain types of cancer, and age-related diseases of the eye. In this study, these chemopreventive activities of a carotenoids-overexpressing transgenic carrot were evaluated. The results of DPPH, hydroxyl, and superoxide radical scavenging tests demonstrate that the acetone extract obtained from the taproots of the carrot plants exhibits significant antioxidant activity. A higher activity was detected in the transgenic carrot extract compared with the wild-type extract. A chemopreventive activity test for degenerative diseases of the eye revealed that pretreatment with the carrot extract reduced cell death in a retinal ganglion cell line, RGC-5 cells exposed to 1-buthionine- (R,S)-sulfoximine and L-glutamic acid.


Asunto(s)
Antioxidantes/farmacología , Carotenoides/farmacología , Daucus carota/genética , Extractos Vegetales/farmacología , Sustancias Protectoras/farmacología , Células Ganglionares de la Retina/efectos de los fármacos , Acetona , Antioxidantes/química , Antioxidantes/metabolismo , Compuestos de Bifenilo , Butionina Sulfoximina/farmacología , Carotenoides/análisis , Muerte Celular , Línea Celular , Daucus carota/metabolismo , Ácido Glutámico/farmacología , Humanos , Radical Hidroxilo/metabolismo , Estrés Oxidativo , Picratos , Extractos Vegetales/química , Raíces de Plantas/genética , Raíces de Plantas/metabolismo , Plantas Modificadas Genéticamente , Células Ganglionares de la Retina/fisiología , Superóxidos/metabolismo
10.
BMC Complement Altern Med ; 12: 230, 2012 Nov 26.
Artículo en Inglés | MEDLINE | ID: mdl-23181522

RESUMEN

BACKGROUND: Centipede grass (CG) originates from China and South America and is reported to contain several C-glycosyl flavones and phenolic constituents, including maysin and luteolin derivatives. This study aimed to investigate, for the first time, the antiobesity activity of CG and its potential molecular mechanism in 3T3-L1 cells. METHODS: To study the effect of CG on adipogenesis, differentiating 3T3-L1 cells were treated every day with CG at various concentrations (0-100 µg/ml) for six days. Oil-red O staining and triglyceride content assay were performed to determine the lipid accumulation in 3T3-L1 cells. The expression of mRNAs or proteins associated with adipogenesis was measured using RT-PCR and Western blotting analysis. We examined the effect of CG on level of phosphorylated Akt in 3T3-L1 cells treated with CG at various concentration s during adipocyte differentiation. RESULTS: Differentiation was investigated with an Oil-red O staining assay using CG-treated 3T3-L1 adipocytes. We found that CG suppressed lipid droplet formation and adipocyte differentiation in 3T3-L1 cells in a dose-dependent manner. Treatment of the 3T3-L1 adipocytes with CG resulted in an attenuation of the expression of adipogenesis-related factors and lipid metabolic genes. The expression of C/EBPα and PPARγ, the central transcriptional regulators of adipogenesis, was decreased by the treatment with CG. The expression of genes involved in lipid metabolism, aP2 were significantly inhibited following the CG treatment. Moreover, the CG treatment down-regulated the phosphorylation levels of Akt and GSK3ß. CONCLUSIONS: Taken collectively, these data indicated that CG exerts antiadipogenic activity by inhibiting the expression of C/EBPß, C/EBPα, and PPARγ and the Akt signaling pathway in 3T3-L1 adipocytes.


Asunto(s)
Adipogénesis/efectos de los fármacos , Proteínas Potenciadoras de Unión a CCAAT/antagonistas & inhibidores , Expresión Génica/efectos de los fármacos , PPAR gamma/antagonistas & inhibidores , Extractos Vegetales/farmacología , Poaceae , Proteínas Proto-Oncogénicas c-akt/metabolismo , Células 3T3-L1 , Adipocitos/efectos de los fármacos , Animales , Fármacos Antiobesidad/farmacología , Proteína alfa Potenciadora de Unión a CCAAT/antagonistas & inhibidores , Proteína beta Potenciadora de Unión a CCAAT/antagonistas & inhibidores , Relación Dosis-Respuesta a Droga , Regulación hacia Abajo , Proteínas de Unión a Ácidos Grasos/genética , Proteínas de Unión a Ácidos Grasos/metabolismo , Flavonoides/farmacología , Glucósidos/farmacología , Glucógeno Sintasa Quinasa 3/metabolismo , Glucógeno Sintasa Quinasa 3 beta , Metabolismo de los Lípidos/efectos de los fármacos , Metabolismo de los Lípidos/genética , Luteolina/farmacología , Ratones , Fosforilación , Polifenoles/farmacología , Transducción de Señal
11.
Anim Sci J ; 83(3): 245-51, 2012 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-22435629

RESUMEN

The effect of by-products of oriental medicinal plants (OMP; T1) containing 0.03% herb extracts (T2) or 0.1% aminolevulinic acid (T3) on the production performance of swine during the finishing period and on its meat quality were investigated. No significant differences were found in the weight gain, feed intake and feed conversion rate among the tested groups (P > 0.05). But the treated group showed higher (P < 0.05) moisture and ash and lower protein than the control group. The T3 group showed a lower meat cholesterol content (38.42 mg/100 g) compared to the other groups (P < 0.05). The vitamin E content of the muscle in the treated groups was higher compared to the control group. No antibiotic content was detected in all treated and control samples. The values of the volatile basic nitrogen (VBN) and thiobarbituric acid reactive substance (TBARS) of the treated groups were significantly lower (P < 0.01) than the control group. The treated groups had significantly better (P < 0.05) sensory-test scores for color, flavor, off-flavor and total acceptability compared to the control group.


Asunto(s)
Carne , Medicina Tradicional Coreana , Porcinos/fisiología , Ácido Aminolevulínico/farmacología , Animales , Colesterol/análisis , Medicina de Hierbas , Carne/análisis , Porcinos/crecimiento & desarrollo , Vitamina E/análisis
12.
Int J Food Sci Nutr ; 63(5): 603-9, 2012 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-22149899

RESUMEN

Herbs and spices not only variety and racy flavour to Korean foods, they also are the richest source for antioxidant power. The present study evaluates the radical scavenging-linked antioxidant activities of hot water extracts from commonly used herbs and spices in Korea. 2,2-Diphenyl-1-picrylhydrazyl (DPPH) radical and superoxide anion scavenging activities of bay extract were 39.5% and 22.1%, respectively. The hydroxyl radical scavenging activity was in order of dill (50.0%) > bay (31.3%) > garlic (27.9%) > white pepper and black pepper (15.1-15.3%) > onion (10.1%) extracts. Bay extract had the highest total phenolic content (17.86 µg CE/g). High correlation coefficients were found between the total phenol content and DPPH radical scavenging activity (R = 0.9162). These results indicate that herbs and spices had high antioxidant activity that is partly due to the phenolic compounds and provide basic data for further development of processed food products.


Asunto(s)
Antioxidantes/farmacología , Magnoliopsida , Fenoles/farmacología , Preparaciones de Plantas/farmacología , Especias , Antioxidantes/análisis , Compuestos de Bifenilo/metabolismo , Depuradores de Radicales Libres/farmacología , Radical Hidroxilo/metabolismo , Corea (Geográfico) , Fenoles/análisis , Picratos/metabolismo , Preparaciones de Plantas/química , Superóxidos/metabolismo
13.
Int J Mol Sci ; 12(6): 4120-31, 2011.
Artículo en Inglés | MEDLINE | ID: mdl-21747728

RESUMEN

Recently, the natural spices and herbs such as rosemary, oregano, and caraway have been used for the processing of meat products. This study investigates the antioxidant activity of 13 spices commonly used in meat processing plants. The hot water extracts were then used for evaluation of total phenolic content, total flavonoids content and antioxidant activities. Our results show that the hot water extract of oregano gave the highest extraction yield (41.33%) whereas mace (7.64%) gave the lowest. The DPPH radical scavenging ability of the spice extracts can be ranked against ascorbic acid in the order ascorbic acid > clove > thyme > rosemary > savory > oregano. The values for superoxide anion radical scavenging activities were in the order of marjoram > rosemary > oregano > cumin > savory > basil > thyme > fennel > coriander > ascorbic acid. When compared to ascorbic acid (48.72%), the hydroxyl radical scavenging activities of turmeric and mace were found to be higher (p < 0.001). Clove had the highest total phenolic content (108.28 µg catechin equivalent (CE)/g). The total flavonoid content of the spices varied from 324.08 µg quercetin equivalent (QE)/g for thyme to 3.38 µg QE/g for coriander. Our results indicate that hot water extract of several spices had a high antioxidant activity which is partly due to the phenolic and flavonoid compounds. This provides basic data, having implications for further development of processed food products.


Asunto(s)
Antioxidantes/química , Carum/química , Origanum/química , Extractos Vegetales/química , Rosmarinus/química , Antioxidantes/aislamiento & purificación , Carum/metabolismo , Flavonoides/química , Flavonoides/aislamiento & purificación , Calor , Origanum/metabolismo , Oxidación-Reducción , Fenoles/química , Fenoles/aislamiento & purificación , Rosmarinus/metabolismo , Agua/química
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