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1.
Food Funct ; 12(4): 1432-1451, 2021 Mar 01.
Artigo em Inglês | MEDLINE | ID: mdl-33533385

RESUMO

Due to the growing global population, reduction in arable land and effects of climate change, incongruity between food supply and demand has become increasingly severe. Nowadays, with awareness of the elementary nutrients required for human growth, increasing attention is being paid to the health and medical functions of food. Along with increased food production achieved by modern agricultural techniques, underutilised functional foods are an important strategy for solving food security problems and maintaining the nutritional quality of the human diet. Rosa roxburghii Tratt (RRT) is a natural fruit that contains unique functional and nutritional constituents, which are characterised by a high anti-oxidant potential. This review summarises the biological characteristics, chemical composition, health-promoting properties and development status of RRT products to inspire investigations on the use of RRT fruit as a functional food, dietary supplement and pharmaceutical additive. The nutrients and functional ingredients of RRT fruit are described in detail to provide more reference information for nutritionists and pharmacists.


Assuntos
Frutas/química , Alimento Funcional , Preparações de Plantas , Rosa , Animais , Antioxidantes , Suplementos Nutricionais , Humanos , Camundongos , Compostos Fitoquímicos/análise , Compostos Fitoquímicos/química
2.
Food Res Int ; 130: 108941, 2020 04.
Artigo em Inglês | MEDLINE | ID: mdl-32156388

RESUMO

Food fermentation can improve food nutritional value and sensory performance, it is considered as an ecofriendly bioprocessing technology. In this work, a fermented natto chestnut food was firstly developed and its active ingredients and functional properties were systematically studied. Through systematic experimental screening, including a single factor experiment and Box-Behnken design, the fermentation parameters of chestnut were optimized and selected. Under the optimal fermentation conditions, fermentation time 56 h, temperature 38 â„ƒ and 5% inoculum concentration, the fibrinolytic activity of the natto-chestnut reached 6479 IU/g. Meanwhile, higher antioxidant activity of the natto-chestnut was obtained due to the increased contents of total phenolic, total flavonoid and VC. In addition, α-glucosidase inhibition activity was also improved in the natto-chestnut. These results indicated that fermented chestnut could be a new dietary supplement with higher quality and better activities for people's health.


Assuntos
Aesculus/microbiologia , Bacillus subtilis/classificação , Bacillus subtilis/metabolismo , Microbiologia de Alimentos , Frutas/metabolismo , Antioxidantes , Fermentação , Frutas/química , Inibidores de Glicosídeo Hidrolases/farmacologia , Probióticos , Subtilisinas/química , Subtilisinas/metabolismo , alfa-Glucosidases/metabolismo
3.
J Sep Sci ; 43(7): 1339-1347, 2020 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-32017401

RESUMO

Taxanes are natural anticancer constituents, and the sample preparation from matrix normally depends on organochlorine solvents. In this study, green and natural menthol-based aqueous deep eutectic solvent was synthesized and used for sample preparation for taxanes. Five key parameters were optimized and the optimal preparation conditions were as follows: menthol/1-propanol ratio 1:1 (mol/mol), solid-liquid ratio 1:30 g/mL, extraction time 30 min, ultrasonic power 250 W, and water content 80%. Under the above conditions, the total extraction efficiency of seven main taxanes was 1.25- to 1.44-fold to the conventional methods. In addition, a high-performance liquid chromatography method with C18 column was established for quantitation of seven main taxanes in <25 min, which had excellent linearity (R2  > 0.9986), precision (relative standard deviation < 3.00%), repeatability (relative standard deviation < 3.69%), and recovery (90.26-109.00%). This method performed the extraction, and enrichment processes simultaneously, and it had advantages such as high extraction efficiency, simple operation, low cost, and eco-friendliness. This work indicated that the natural menthol-based deep eutectic solvent aqueous could be an excellent alternative to the sample preparation from Taxus or other plants.


Assuntos
Antineoplásicos Fitogênicos/análise , Mentol/química , Taxoides/análise , Taxus/química , Cromatografia Líquida de Alta Pressão , Mentol/síntese química , Solventes/síntese química , Solventes/química , Água/química
4.
J Pharm Biomed Anal ; 170: 335-340, 2019 Jun 05.
Artigo em Inglês | MEDLINE | ID: mdl-30986686

RESUMO

In this study, an efficient and sensitive UHPLC-QQQ-MS/MS (MRM) analytical strategy was established firstly for simultaneous determination of 11 components, including 3 original flavonol glycoside, 4 terpene lactones and 4 biflavonoids in Ginkgo biloba leaves. The validated strategy exhibited proper linearity (R2 ≥0.99) in the range of 0.5-125 µg/mL, and intra and inter-day precision were lower than 4.09% and 4.80%, respectively. Limit of detection (LOD) and quantification (LOQ) were calculated, ranging from 0.2-4.6 ng/mL, with repeatability values between 1.98% and 4.48%. The average recoveries were all in the range of 98.45-106.67% with RSD (n = 3) for the related compounds. Subsequently, the proposed method was used for the analysis of Ginkgo biloba leaves during leaf senescence. Results showed the dominant flavonol glycosides were kaempferol-3-O-rutinoside and isorhamnetin-3-O-rutinoside, the level of terpene lactones and biflavonoids reached the highest in the latest harvest samples. Compared with conventional detection method, the present method could directly analyze original flavonol glycoside without acid hydrolysis process and terpene lactones without the ELSD in a high sensitivity. Moreover, the biflavonoids in Ginkgo biloba leaves were also simultaneously quantified. The results demonstrated that the developed method was accurate, sensitive and reliable for simultaneous quantification of multi-components in Ginkgo biloba leaves, and this study should be significant for the comprehensive utilization and development of Ginkgo biloba resources.


Assuntos
Biflavonoides/química , Glicosídeos Cardíacos/química , Flavonóis/química , Ginkgo biloba/química , Lactonas/química , Espectrometria de Massas em Tandem/métodos , Terpenos/química , Cromatografia Líquida de Alta Pressão/métodos , Dissacarídeos/química , Flavonoides/química , Quempferóis/química , Extratos Vegetais/química , Folhas de Planta/química
5.
J Mol Cell Biol ; 7(4): 326-37, 2015 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-26169120

RESUMO

Haploid pluripotent stem cells, such as haploid embryonic stem cells (haESCs), facilitate the genetic study of recessive traits. In vitro, fish haESCs maintain haploidy in both undifferentiated and differentiated states, but whether mammalian haESCs can preserve pluripotency in the haploid state has not been tested. Here, we report that mouse haESCs can differentiate in vitro into haploid epiblast stem cells (haEpiSCs), which maintain an intact haploid genome, unlimited self-renewal potential, and durable pluripotency to differentiate into various tissues in vitro and in vivo. Mechanistically, the maintenance of self-renewal potential depends on the Activin/bFGF pathway. We further show that haEpiSCs can differentiate in vitro into haploid progenitor-like cells. When injected into the cytoplasm of an oocyte, androgenetic haEpiSC (ahaEpiSCs) can support embryonic development until midgestation (E12.5). Together, these results demonstrate durable pluripotency in mouse haESCs and haEpiSCs, as well as the valuable potential of using these haploid pluripotent stem cells in high-throughput genetic screening.


Assuntos
Camadas Germinativas/citologia , Haploidia , Células-Tronco Embrionárias Murinas/citologia , Células-Tronco Pluripotentes/citologia , Animais , Diferenciação Celular , Citoplasma/metabolismo , Diploide , Desenvolvimento Embrionário , Humanos , Masculino , Camundongos , Camundongos SCID
7.
Nature ; 490(7420): 407-11, 2012 Oct 18.
Artigo em Inglês | MEDLINE | ID: mdl-23023130

RESUMO

Haploids and double haploids are important resources for studying recessive traits and have large impacts on crop breeding, but natural haploids are rare in animals. Mammalian haploids are restricted to germline cells and are occasionally found in tumours with massive chromosome loss. Recent success in establishing haploid embryonic stem (ES) cells in medaka fish and mice raised the possibility of using engineered mammalian haploid cells in genetic studies. However, the availability and functional characterization of mammalian haploid ES cells are still limited. Here we show that mouse androgenetic haploid ES (ahES) cell lines can be established by transferring sperm into an enucleated oocyte. The ahES cells maintain haploidy and stable growth over 30 passages, express pluripotent markers, possess the ability to differentiate into all three germ layers in vitro and in vivo, and contribute to germlines of chimaeras when injected into blastocysts. Although epigenetically distinct from sperm cells, the ahES cells can produce viable and fertile progenies after intracytoplasmic injection into mature oocytes. The oocyte-injection procedure can also produce viable transgenic mice from genetically engineered ahES cells. Our findings show the developmental pluripotency of androgenentic haploids and provide a new tool to quickly produce genetic models for recessive traits. They may also shed new light on assisted reproduction.


Assuntos
Androgênios/metabolismo , Células-Tronco Embrionárias/fisiologia , Haploidia , Camundongos Transgênicos/crescimento & desenvolvimento , Animais , Biomarcadores/metabolismo , Blastocisto/citologia , Linhagem Celular , Núcleo Celular , Quimera/embriologia , Quimera/genética , Células-Tronco Embrionárias/citologia , Epigênese Genética , Feminino , Masculino , Camundongos , Camundongos Transgênicos/embriologia , Camundongos Transgênicos/genética , Modelos Animais , Modelos Genéticos , Oócitos/citologia , Oócitos/crescimento & desenvolvimento , Oócitos/metabolismo , Células-Tronco Pluripotentes/citologia , Células-Tronco Pluripotentes/fisiologia , Injeções de Esperma Intracitoplásmicas , Espermatozoides/metabolismo , Espermatozoides/transplante
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