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1.
J Sci Food Agric ; 99(8): 4063-4071, 2019 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-30761529

RESUMEN

BACKGROUND: Edible packaging and coating with natural antimicrobials such as essential oils is an emerging technology for the control of pathogen growth in meat products. This study aimed to explore ethyl cellulose (EC) of three viscosities for the structuring of cinnamon essential oil (CEO), and investigated the physicochemical properties of the resulting oleogel and its emulsion, as well as the corresponding antibacterial activity in model and actual environments (as in sausages). RESULTS: The network structure of CEO-EC oleogel was more compact with increased EC viscosity, thereby improving the binding capacity and stability of the oil. A positive correlation was found between EC viscosity and particle size of the CEO-EC emulsion. The 45 cP CEO-EC emulsion exhibited greatest antimicrobial activitiy in models with Escherichia coli (E. coli) O157:H7 (ATCC 700927) and Staphylococcus aureus (S. aureus) (ATCC 29213), as well as in sausage, with respect to total counts of mesophilic bacteria, psychrotrophs, lactobacilli, and pseudomonads. CONCLUSION: The CEO-EC oleogel has antibacterial activity, determined by the EC viscosity, that provide potential antibacterial protection for meat products and might be especially suitable for some traditional Chinese ready-to-eat sausages without strictly sealed packaging. © 2019 Society of Chemical Industry.


Asunto(s)
Antibacterianos/química , Celulosa/análogos & derivados , Cinnamomum zeylanicum/química , Aceites Volátiles/química , Aceites Volátiles/farmacología , Aceites de Plantas/química , Antibacterianos/farmacología , Celulosa/química , Escherichia coli O157/efectos de los fármacos , Escherichia coli O157/crecimiento & desarrollo , Listeria monocytogenes/efectos de los fármacos , Listeria monocytogenes/crecimiento & desarrollo , Pruebas de Sensibilidad Microbiana , Compuestos Orgánicos/química , Compuestos Orgánicos/farmacología , Aceites de Plantas/farmacología , Staphylococcus aureus/efectos de los fármacos , Staphylococcus aureus/crecimiento & desarrollo , Viscosidad
2.
BMC Dev Biol ; 14: 16, 2014 Apr 21.
Artículo en Inglés | MEDLINE | ID: mdl-24750690

RESUMEN

BACKGROUND: The miniature pig provides an excellent experimental model for tooth morphogenesis because its diphyodont and heterodont dentition resembles that of humans. However, little information is available on the process of tooth development or the exact molecular mechanisms controlling tooth development in miniature pigs or humans. Thus, the analysis of gene expression related to each stage of tooth development is very important. RESULTS: In our study, after serial sections were made, the development of the crown of the miniature pigs' mandibular deciduous molar could be divided into five main phases: dental lamina stage (E33-E35), bud stage (E35-E40), cap stage (E40-E50), early bell stage (E50-E60), and late bell stage (E60-E65). Total RNA was isolated from the tooth germ of miniature pig embryos at E35, E45, E50, and E60, and a cDNA library was constructed. Then, we identified cDNA sequences on a large scale screen for cDNA profiles in the developing mandibular deciduous molars (E35, E45, E50, and E60) of miniature pigs using Illumina Solexa deep sequencing. Microarray assay was used to detect the expression of genes. Lastly, through Unigene sequence analysis and cDNA expression pattern analysis at E45 and E60, we found that 12 up-regulated and 15 down-regulated genes during the four periods are highly conserved genes homologous with known Homo sapiens genes. Furthermore, there were 6 down-regulated and 2 up-regulated genes in the miniature pig that were highly homologous to Homo sapiens genes compared with those in the mouse. CONCLUSION: Our results not only identify the specific transcriptome and cDNA profile in developing mandibular deciduous molars of the miniature pig, but also provide useful information for investigating the molecular mechanism of tooth development in the miniature pig.


Asunto(s)
Biblioteca de Genes , Diente Molar/metabolismo , Porcinos Enanos/genética , Diente Primario/metabolismo , Animales , Análisis por Conglomerados , Regulación del Desarrollo de la Expresión Génica , Ontología de Genes , Humanos , Mandíbula/embriología , Mandíbula/metabolismo , Ratones , Diente Molar/embriología , Odontogénesis/genética , Análisis de Secuencia por Matrices de Oligonucleótidos , Reacción en Cadena de la Polimerasa de Transcriptasa Inversa , Porcinos , Porcinos Enanos/embriología , Factores de Tiempo , Germen Dentario/embriología , Germen Dentario/metabolismo , Diente Primario/embriología , Transcriptoma/genética
3.
Medicine (Baltimore) ; 98(40): e17471, 2019 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-31577778

RESUMEN

Hand, foot, and mouth disease (HFMD) spreads rapidly and has been recognized as a public health problem in recent years in China. Unfortunately, there is no effective vaccine or antiviral drug currently for EV71 infection. In this study, we aim to identify biomarker which are associated with for severity of EV71 infection cases using high-throughput RNA sequencing approach.RNA sequencing of samples from severe HFMD (S) patients group (n = 10) and control HFMD (C) patients group (n = 10) were performed and the results were verified by qPCR. mRNA with the highest expression level was selected to be validated in an independent cohort comprising of 45 severe EV71 infected patients and 45 control by qPCR assay.Seventeen significant differentially expressed genes were identified. Scavenger receptor class A, member 3 (SCARA3) was one of the significantly upregulated genes with the highest expression level and was selected for validation. The mean relative expression levels in severe HFMD and control HFMD patients were 10.1-fold and 5.0-fold, respectively, P value <.001.We found that SCARA3 is associated with severity of HFMD, and it may be a potential prognostic marker to predict the HFMD progression in EV71 infected patients.


Asunto(s)
Enfermedad de Boca, Mano y Pie/diagnóstico , Enfermedad de Boca, Mano y Pie/genética , Proteínas de Choque Térmico/genética , Receptores Depuradores de Clase A/genética , Biomarcadores/metabolismo , Estudios de Casos y Controles , Preescolar , Femenino , Enfermedad de Boca, Mano y Pie/metabolismo , Proteínas de Choque Térmico/metabolismo , Humanos , Lactante , Masculino , ARN Mensajero/metabolismo , Receptores Depuradores de Clase A/metabolismo , Índice de Severidad de la Enfermedad
4.
Guang Pu Xue Yu Guang Pu Fen Xi ; 27(12): 2448-52, 2007 Dec.
Artículo en Zh | MEDLINE | ID: mdl-18330282

RESUMEN

Diagenetic effect during burial on the hydroxyapatite in enamel and dentin from fossil human and animal teeth was examined, using X-ray diffraction (XRD) and Fourier transform infrared spectroscopy (FTIR). For the enamel and dentin of all fossil teeth, XRD patterns exhibit bulge line and overlap between major reflections of hydroxyapatite, and the crystallinity of hydroxyapatite is low. For each infrared spectrum, H2O and OH(-) have distinct peaks of absorbance, and PO4(3-) and CO3(2-) ions have intensive infrared vibration modes at the fundamental wave numbers. The component of hydroxyapatite of all fossil teeth is similar to the modern biological hydroxyapatite. Furthermore, the index (PCI) which reflects the hydroxyapatite crystallinity of each sample ranges from 2.4 to 4.0 while the index (BPI) reflecting the amount of type B carbonate to phosphate indicates that the values of CO3(2-) content in hydroxyapatite are rather high, accordingly the crystallinity of all fossil hydroxyapatites are poor. It could be concluded that little alteration of hydroxyapatites from fossil human and animal teeth occurred in the process of diagenesis in Jinsha Relict, Chengdu, China.


Asunto(s)
Durapatita/análisis , Fósiles , Paleodontología/métodos , Espectroscopía Infrarroja por Transformada de Fourier/métodos , Diente/química , Difracción de Rayos X/métodos , Animales , China , Humanos
5.
Biomaterials ; 27(20): 3758-65, 2006 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-16549197

RESUMEN

As a prerequisite for tissue engineering applications, researchers must understand the effect on local cell types of the degradation products of biodegradable polymers. Polyhydroxybutyrate (PHB) has received special interest as an implant material, because it degrades to release a normal component of blood and tissue, D,L-beta-hydroxybutyrate (HB). We report that HB (0.02 g/l) promoted cell proliferation in cultured L929 cells plated at high cell density (1 x 10(5) cells/well) but not lower cell densities. While HB did not affect cell cycle progression, it significantly inhibited cell death. HB treatment prevented necrosis, reducing cell membrane permeability 4h following serum withdrawal from the medium, and for all subsequent time points. In summary, HB promotes proliferation of L929 cells in high-density cultures by preventing apoptotic and necrotic cell death. This property makes biodegradable polymers containing HB, such as PHBHHx, attractive candidates for tissue engineering applications, especially those requiring the regeneration of large numbers of cells.


Asunto(s)
Ácido 3-Hidroxibutírico/farmacología , Materiales Biocompatibles/metabolismo , Muerte Celular/efectos de los fármacos , Proliferación Celular/efectos de los fármacos , Animales , Ciclo Celular/efectos de los fármacos , Línea Celular , Ratones , Polímeros/metabolismo
6.
ACS Nano ; 7(9): 8251-7, 2013 Sep 24.
Artículo en Inglés | MEDLINE | ID: mdl-23972012

RESUMEN

The orientation and spatial distribution of nanocrystals in the organic matrix are two distinctive structural characteristics associated with natural bone. Synthetic soft materials have been used to successfully control the orientation of mineral crystals. The spatial distribution of minerals in a synthetic scaffold, however, has yet to be reproduced in a biomimetic manner. Herein, we report using block copolymer-decorated polymer nanofibers to achieve biomineralized fibrils with precise control of both mineral crystal orientation and spatial distribution. Exquisite nanoscale structural control in biomimetic hybrid materials has been demonstrated.


Asunto(s)
Resinas Acrílicas/síntesis química , Materiales Biomiméticos/síntesis química , Sustitutos de Huesos/síntesis química , Cristalización/métodos , Nanofibras/química , Nanofibras/ultraestructura , Poliésteres/síntesis química , Ensayo de Materiales , Conformación Molecular , Tamaño de la Partícula , Propiedades de Superficie
7.
Biomacromolecules ; 6(2): 593-7, 2005.
Artículo en Inglés | MEDLINE | ID: mdl-15762618

RESUMEN

Poly(hydroxybutyrate-co-hydroxyhexanoate) (PHBHHx), a member of the polyhydroxyalkanoate family of biopolyesters, has superior mechanical properties and biocompatibilities that enable it to meet diverse biomedical requirements. The main component of PHBHHx is DL-beta-hydroxybutyric acid (HB), a ketone body that is also produced in vivo. The effects of HB treatment on murine fibroblast L929 cells, human umbilical vein endothelial cells, and rabbit articular cartilages were investigated. HB (0.005-0.10 g/L) promoted cell proliferation for each cell line. Cell cycle analysis indicated that HB had a stimulatory effect on DNA synthesis. Flow cytometric analysis of L929 cells revealed changes in the [Ca2+]i for different stages of the cell cycle. In L929 cells, HB (0.02 g/L) stimulated a rapid increase in the concentration of cytosolic calcium that was blocked by verapamil and diltiazem, inhibitors of L-type Ca2+ channels. Finally, verapamil inhibited HB-induced L929 cell proliferation. Collectively, these results indicated that HB had a stimulatory effect on cell cycle progression that is mediated by a signaling pathway dependent upon increases in [Ca2+]i. This trophic effect may underlie the good biocompatibility observed for PHBHHx.


Asunto(s)
Ácido 3-Hidroxibutírico/farmacología , Calcio/metabolismo , Proliferación Celular/efectos de los fármacos , Animales , Materiales Biocompatibles , Transporte Biológico/efectos de los fármacos , Caproatos , Cartílago Articular/citología , Cartílago Articular/efectos de los fármacos , Ciclo Celular , Línea Celular , Endotelio Vascular/citología , Endotelio Vascular/efectos de los fármacos , Fibroblastos/citología , Fibroblastos/efectos de los fármacos , Humanos , Ratones , Conejos , Transducción de Señal , Venas Umbilicales
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