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1.
Opt Express ; 26(22): 28429-28440, 2018 Oct 29.
Artículo en Inglés | MEDLINE | ID: mdl-30470014

RESUMEN

Silicon-on-chip photonic circuits are among some very promising platforms for generating nonclassical photonic quantum state, because of its low loss, small footprint, and compatibility with complementary metal-oxide-semiconductor (CMOS) and telecommunications techniques. Dense wavelength division multiplexing (DWDM) is a leading technique for enhancing the transmission capacity of both classical and quantum communications. To bridge the frequency gap between silicon-chip and other quantum systems, such as quantum memories, a quantum interface is indispensable. Here, we demonstrate a quantum interface for multiplexed energy-time entanglement states, which are generated on a silicon micro-ring cavity that is based on frequency up-conversion. By switching the pump wavelength, energy-time entanglement from any channel can be selected at will after being up-converted. The high visibilities of two-photon interference over three channels after frequency up-conversion clearly prove that the entanglement is fully preserved during the quantum frequency conversion (QFC) process. Our work provides new perspectives regarding channel capacity enhancement in quantum communications and for quantum resources being transferred between two different quantum systems.

2.
Mol Med Rep ; 17(4): 5894-5902, 2018 04.
Artículo en Inglés | MEDLINE | ID: mdl-29436695

RESUMEN

The present study aimed to explore the effects of n­3 polyunsaturated fatty acids (PUFAs) on autophagy and their potential for promoting locomotor recovery after spinal cord injury (SCI). Primary neurons were isolated and cultured. Sprague­Dawley rats were randomly divided into three groups and fed diets with different amounts of n­3 PUFAs. A model of spinal cord contusion was created at the T10 spinal segment and the composition of PUFAs was analyzed using gas chromatography. Spinal repair and motor function were evaluated postoperatively. Assessment of the effects of n­3 PUFAs on autophagy and mammalian target of rapamycin complex 1 (mTORC1) was performed using immunofluorescence staining and western blotting. In vitro, n­3 PUFAs inhibited mTORC1 and enhanced autophagy. The n­3 PUFA levels and the ratio of n­3 PUFA to n­6 PUFA in the spinal cord and serum of rats fed a high­n­3 PUFA diet were higher before and after operation (P<0.05). Additionally, rats in the high­n­3 PUFA group showed improved motor function recovery, spinal cord repair­related protein expression level (MBP, Galc and GFAP). Expression levels if these protiens in the high­n­3 PUFA diet group expressed the highest levels, followed by the low­n­3 PUFA diet group and finally the control group (P<0.05). high­n­3 PUFA diet promoted autophagy ability and inhibited activity of the mTORC1 signaling pathway compared with the low­n­3 PUFA diet group or the control group (P<0.05). These results suggest that exogenous dietary n­3 PUFAs can inhibit mTORC1 signaling and enhance autophagy, promoting functional recovery of rats with SCI.


Asunto(s)
Ácidos Grasos Omega-3/farmacología , Diana Mecanicista del Complejo 1 de la Rapamicina/metabolismo , Actividad Motora/efectos de los fármacos , Recuperación de la Función/efectos de los fármacos , Transducción de Señal/efectos de los fármacos , Traumatismos de la Médula Espinal/metabolismo , Traumatismos de la Médula Espinal/fisiopatología , Animales , Autofagia/efectos de los fármacos , Autofagia/genética , Conducta Animal , Dieta , Grasas de la Dieta , Modelos Animales de Enfermedad , Femenino , Expresión Génica , Neuronas/efectos de los fármacos , Neuronas/metabolismo , Ratas , Traumatismos de la Médula Espinal/tratamiento farmacológico , Traumatismos de la Médula Espinal/etiología
3.
Oncol Rep ; 39(1): 129-137, 2018 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-29115548

RESUMEN

BC (BC), as the most common malignancy in women worldwide, is associated with high morbidity and mortality. However, chemoresistance and toxicity are the main causes that limit the success of treatment in aggressive BC cases. Thus, there is a vital need to identify and develop novel therapeutic agents. Frankincense, pine needle and geranium essential oils have been reported to play critical biological activities in cancer. However, to the best of our knowledge whether frankincense, pine needle and geranium essential oils have any effect on the progression of BC in MCF-7 cells remains unclear. In the present study, we assessed the possible effects of frankincense, pine needle and geranium essential oils on cell viability, proliferation, migration and invasion as well as the possible mechanisms. MCF-7 cells were treated with oils, and associations with BC were investigated. In the present study, we clearly revealed that frankincense, pine needle and geranium essential oils suppressed cell viability, proliferation, migration and invasion in human BC MCF-7 cells. Further data demonstrated that frankincense, pine needle and geranium essential oils induced apoptosis, but did not affect cell cycle progression. Consistent with the in vitro activities, frankincense essential oil was effective in inhibiting tumor growth and inducing tumor cell apoptosis in a human BC mouse model. In addition, these 3 essential oils modulated the activity of the AMPK/mTOR signaling pathway. In conclusion, the present study indicated that frankincense, pine needle and geranium essential oils were involved in the progression of BC cells possibly through the AMPK/mTOR pathway.


Asunto(s)
Neoplasias de la Mama/metabolismo , Olíbano/química , Geranium/química , Aceites Volátiles/farmacología , Pinus/química , Transducción de Señal/efectos de los fármacos , Adenilato Quinasa/metabolismo , Animales , Neoplasias de la Mama/tratamiento farmacológico , Movimiento Celular/efectos de los fármacos , Proliferación Celular/efectos de los fármacos , Supervivencia Celular/efectos de los fármacos , Femenino , Regulación Neoplásica de la Expresión Génica/efectos de los fármacos , Humanos , Células MCF-7 , Ratones , Invasividad Neoplásica , Aceites de Plantas/farmacología , Serina-Treonina Quinasas TOR/metabolismo , Ensayos Antitumor por Modelo de Xenoinjerto
4.
Exp Parasitol ; 146: 1-10, 2014 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-25173485

RESUMEN

Toxoplasma gondii Glutathione Reductase (TgGR) plays important role during the survival of the parasite. In this investigation, immunological changes and protection efficiency of this protein delivered as a DNA vaccine (pTgGR) have been evaluated. Mice were immunized with pTgGR, followed by challenge with virulent T. gondii RH strain, 2 weeks after the booster immunization. Compared to the control groups pVAX1, PBS and Blank groups, the results showed that pTgGR stimulated specific humoral response defined by significant titers of total IgG, subclasses IgG1 and IgG2a, classes IgA and IgM, but not IgE. Analysis of IFN-γ, IL-4, IL-17 and TGF-ß1 cytokines after immunization and compared with the control groups showed significant increments in pTgGR group. Additionally, T lymphocytes subpopulation CD4(+) T was positively recruited with significant percentage detected, while subset CD8(+) appeared not to be involved in response to this antigen. Vaccinated mice showed a significantly longer survival time, 15 days, in contrast with control groups which died within 8-10 days after challenge. These results demonstrated that TgGR could induce significant humoral and cell mediated responses leading to a considerable level of resistance against toxoplasmosis infection.


Asunto(s)
Glutatión Reductasa/inmunología , Vacunas Antiprotozoos/inmunología , Toxoplasma/inmunología , Toxoplasmosis Animal/prevención & control , Vacunas de ADN/inmunología , Animales , Relación CD4-CD8 , Citocinas/sangre , Citocinas/metabolismo , Femenino , Glutatión Reductasa/genética , Inmunidad Celular , Inmunoglobulinas/sangre , Inmunoglobulinas/inmunología , Ratones , Plásmidos , Distribución Aleatoria , Ratas , Proteínas Recombinantes/genética , Proteínas Recombinantes/inmunología , Selenio/metabolismo , Bazo/citología , Subgrupos de Linfocitos T/clasificación , Subgrupos de Linfocitos T/citología , Toxoplasma/enzimología , Toxoplasma/patogenicidad , Toxoplasmosis Animal/inmunología , Toxoplasmosis Animal/mortalidad , Virulencia
5.
J Vet Sci ; 13(1): 49-58, 2012 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-22437536

RESUMEN

The complete coding sequence of Haemonchus (H.) contortus HC29 cDNA was generated by rapid amplification of cDNA ends in combination with PCR using primers targeting the 5'- and 3'-ends of the partial mRNA sequence. The cloned HC29 cDNA was shown to be 1,113 bp in size with an open reading frame of 507 bp, encoding a protein of 168 amino acid with a calculated molecular mass of 18.9 kDa. Amino acid sequence analysis revealed that the cloned HC29 cDNA contained the conserved catalytic triad and dimer interface of selenium-independent glutathione peroxidase (GPX). Alignment of the predicted amino acid sequences demonstrated that the protein shared 44.7~80.4% similarity with GPX homologues in the thioredoxin-like family. Phylogenetic analysis revealed close evolutionary proximity of the GPX sequence to the counterpart sequences. These results suggest that HC29 cDNA is a GPX, a member of the thioredoxin-like family. Alignment of the nucleic acid and amino acid sequences of HC29 with those of the reported selenium-independent GPX of H. contortus showed that HC29 contained different types of spliced leader sequences as well as dimer interface sites, although the active sites of both were identical. Enzymatic analysis of recombinant prokaryotic HC29 protein showed activity for the hydrolysis of H(2)O(2). These findings indicate that HC29 is a selenium-independent GPX of H. contortus.


Asunto(s)
Glutatión Peroxidasa/genética , Glutatión Peroxidasa/metabolismo , Hemoncosis/veterinaria , Haemonchus/enzimología , Haemonchus/genética , Secuencia de Aminoácidos , Animales , Secuencia de Bases , Clonación Molecular , ADN Complementario/genética , ADN Complementario/aislamiento & purificación , Enfermedades de las Cabras/parasitología , Cabras , Hemoncosis/parasitología , Hemoncosis/prevención & control , Peróxido de Hidrógeno/metabolismo , Datos de Secuencia Molecular , Filogenia , ARN de Helminto/química , ARN de Helminto/genética , Técnica del ADN Polimorfo Amplificado Aleatorio , Ratas , Ratas Sprague-Dawley , Alineación de Secuencia , Análisis de Secuencia de ADN
6.
Vaccine ; 24(49-50): 7109-14, 2006 Nov 30.
Artículo en Inglés | MEDLINE | ID: mdl-16887240

RESUMEN

Two compound Chinese herbal medicinal ingredients (cCHMIs) were prepared, respectively, with epimedium polysaccharide plus propolis flavone (cCHMIs 1) and astragalus polysaccharide plus ginsenoside (cCHMIs 2). In animal immune experiment, Newcastle disease vaccine was mixed, respectively, with two cCHMIs and IL-2 to vaccinate 15-day-old chicken in experimental groups. On days 7, 14, 21 and 28 after vaccination, the dynamic changes of serum antibody titers were tested by micro-method. In gene expression experiment, each cCHMIs, at three concentrations, was added into cultured chicken peripheral T lymphocyte. After cultivation of 7h, the expression of IL-2 mRNA in the cell, 24h, IFN-gamma mRNA, were determined by semi-quantitative RT-PCR assay. The results showed that two cCHMIs, whether single or cooperative injection with IL-2, could significantly raise the antibody titers, while immunologic synergisms of two cCHMIs with IL-2 were unconspicuous. cCHMs 1 at three doses and cCHMIs 2 at high dose could remarkably promote the expression of IL-2 mRNA in chicken T lymphocyte, two cCHMIs at three doses, the expression of IFN-gamma mRNA, which could explain why the immunologic synergism of cCHMIs with IL-2 was not obvious.


Asunto(s)
Adyuvantes Inmunológicos , Pollos/inmunología , Medicamentos Herbarios Chinos/farmacología , Interferón gamma/biosíntesis , Interleucina-2/biosíntesis , Interleucina-2/farmacología , ARN Mensajero/biosíntesis , Linfocitos T/efectos de los fármacos , Linfocitos T/inmunología , Animales , Anticuerpos Antivirales/análisis , Anticuerpos Antivirales/biosíntesis , Ginsenósidos/química , Ginsenósidos/farmacología , Masculino , Enfermedad de Newcastle/prevención & control , Virus de la Enfermedad de Newcastle/inmunología , Própolis/farmacología , Reacción en Cadena de la Polimerasa de Transcriptasa Inversa , Estimulación Química , Vacunas de Productos Inactivados/inmunología , Vacunas Virales/inmunología
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