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1.
Braz. j. med. biol. res ; 49(2): e4543, 2016. graf
Artículo en Inglés | LILACS | ID: biblio-951657

RESUMEN

High plasma levels of homocysteine (Hcy) promote the progression of neurodegenerative diseases. However, the mechanism by which Hcy mediates neurotoxicity has not been elucidated. We observed that upon incubation with Hcy, the viability of a neuroblastoma cell line Neuro2a declined in a dose-dependent manner, and apoptosis was induced within 48 h. The median effective concentration (EC50) of Hcy was approximately 5 mM. Glyceraldehyde-3-phosphate dehydrogenase (GAPDH) nuclear translocation and acylation has been implicated in the regulation of apoptosis. We found that nuclear translocation and acetylation of GAPDH increased in the presence of 5 mM Hcy and that higher levels of acetyltransferase p300/CBP were detected in Neuro2a cells. These findings implicate the involvement of GAPDH in the mechanism whereby Hcy induces apoptosis in neurons. This study highlights a potentially important pathway in neurodegenerative disorders, and a novel target pathway for neuroprotective therapy.


Asunto(s)
Animales , Conejos , Apoptosis/efectos de los fármacos , Fármacos Neuroprotectores/farmacología , Gliceraldehído-3-Fosfato Deshidrogenasas/metabolismo , Homocisteína/farmacología , Acetilación , Acetiltransferasas/análisis , Factores de Tiempo , Recuento de Células , Extractos Celulares/química , Núcleo Celular/metabolismo , Supervivencia Celular/fisiología , Inducción Enzimática , Western Blotting , Técnica del Anticuerpo Fluorescente , Apoptosis/fisiología , Fármacos Neuroprotectores/administración & dosificación , Línea Celular Tumoral , Factores de Transcripción p300-CBP/metabolismo , Homocisteína/administración & dosificación
2.
Biol. Res ; 47: 1-11, 2014. graf, tab
Artículo en Inglés | LILACS | ID: biblio-950720

RESUMEN

BACKGROUND: Unstable generation of free radicals in the body are responsible for many degenerative diseases. A bloom forming algae Euglena tuba growing abundantly in the aquatic habitats of Cachar district in the state of Assam in North-East India was analysed for its phytochemical contents, antioxidant activity as well as free radical scavenging potentials. RESULTS: Based on the ability of the extract in ABTS•+ radical cation inhibition and Fe3+ reducing power, the obtained results revealed the prominent antioxidant activity of the algae, with high correlation coefficient of its TEAC values to the respective phenolic and flavonoid contents. The extract had shown its scavenging activity for different free radicals and 41.89 ± 0.41 µg/ml, 5.83 ± 0.07 µg/ml, 278.46 ± 15.02 µg/ml and 223.25 ± 4.19 µg/ml were determined as the IC50 values for hydroxyl, superoxide, nitric oxide and hypochlorous acid respectively, which are lower than that of the corresponding reference standards. The phytochemical analysis also revealed that the phenolics, flavonoids, alkaloids, tannins and carbohydrates are present in adequate amount in the extract which was confirmed by HPLC analysis. CONCLUSIONS: The results showed that 70% methanol extract of the algae possesses excellent antioxidant and free radical scavenging properties.


Asunto(s)
Animales , Masculino , Ratones , Extractos Celulares/química , Depuradores de Radicales Libres/metabolismo , Sustancias Reductoras/metabolismo , Euglena/química , Antioxidantes/metabolismo , Oxidación-Reducción , Fenoles/análisis , Ácido Ascórbico/análisis , Taninos/análisis , Flavonoides/análisis , Peroxidación de Lípido/efectos de los fármacos , Cromanos/metabolismo , Cromatografía Líquida de Alta Presión , Metanol , Alcaloides/análisis , Microalgas , Glucosa/análisis , India
3.
Experimental & Molecular Medicine ; : 496-499, 2002.
Artículo en Inglés | WPRIM | ID: wpr-13037

RESUMEN

Human papillomavirus E7 (HPV E7) is a viral oncoprotein that plays an important role in cervical carcinogenesis through binding with retinoblastoma protein (Rb). Inactivation of Rb by E7 is necessary but not sufficient for cellular transformation, suggesting other protein-protein interactions are required for E7-mediated cellular transformation aside from the interaction with Rb. However, studies on the oncogenic function of HPV E7 have been limited by its poor immunoreactivity. In this report, we show that the fixation of purified recombinant HPV E7 on blotted nitrocellulose membrane with glutaldehyde markedly enhanced the immunoreactivity of HPV E7 protein. Using HeLa and Caski cell line which are infected with HPV 18 and HPV 16, respectively, we demonstrated that native HPV E7 proteins also could be detected by this method. These results therefore can provide the experimental conditions for detection of HPV E7 proteins with greater sensitivity and may help to analyze E7 functions.


Asunto(s)
Humanos , Extractos Celulares/química , Línea Celular , Inmunoquímica/métodos , Proteínas Oncogénicas Virales/análisis , Papillomaviridae/química
4.
Acta bioquím. clín. latinoam ; 27(2): 243-50, jun. 1993. ilus, tab
Artículo en Español | LILACS | ID: lil-125911

RESUMEN

El n-dodecil sarcosinato de sodio produce la solubilización del espermatozoide humano con algo de contaminación acrosomal. El extracto está compuesto por una mezcla de productos con pesos moleculares y características inmunológicas similares a las del plasma seminal humano. El hecho de que la antigenicidad se mantenga luego de la solubilización, hace que ésta sea un comienzo útil en el aislamiento de moléculas que juegan un papel en la infertilidad por causas inmunológicas


Asunto(s)
Humanos , Masculino , Extractos Celulares/análisis , Membrana Celular/efectos de los fármacos , Infertilidad Masculina/diagnóstico , Sarcosina , Espermatozoides/ultraestructura , Extractos Celulares/química , Extractos Celulares/inmunología , Infertilidad Masculina/inmunología , Interacciones Espermatozoide-Óvulo , Interacciones Espermatozoide-Óvulo/inmunología , Semen/química , Semen/inmunología , Espermatozoides/efectos de los fármacos , Espermatozoides/inmunología
5.
Artículo en Inglés | IMSEAR | ID: sea-22937

RESUMEN

Angiogenic factors were isolated by ion exchange chromatography from three established cell lines viz., HEp 2, HeLa and CHO, a primary culture of mouse mammary adenocarcinoma and from conditioned media of HEp2 and cultured mammary adenocarcinoma cells. The angiogenic activity was assayed by chicken chorioallantoic membrane assay. The angiogenic factor eluted at 0.5 M, exhibited lambda max at 258 +/- 1 nm, contained protein and nucleic acid. The cellular angiogenic factor showed a ratio of 1:1 for protein and nucleic acid whereas the secreted angiogenic factor had 3-5 parts of protein to 1 part of nucleic acid. The angiogenic factor from HEp2 and CHO cells did not bind to heparin-agarose. Microheterogeneity of the angiogenic factors was established by SDS-PAGE. Antiserum raised against the cellular angiogenic factor from HEp2 cells, showed a titre of 1:1600 by ELISA. The angiogenic factor was directly localized on whole cells by ELISA. Cellular as well as secreted angiogenic factors crossreacted with the antibody. Neutralizing effect of the antiserum on induction of angiogenesis was detected on chicken chorioallantoic membrane.


Asunto(s)
Inductores de la Angiogénesis/análisis , Animales , Células CHO , Extractos Celulares/química , Cricetinae , Medios de Cultivo Condicionados/química , Femenino , Células HeLa , Humanos , Ratones , Células Tumorales Cultivadas
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