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1.
Hist. ciênc. saúde-Manguinhos ; 21(4): 1131-1149, Oct-Dec/2014.
Artículo en Portugués | LILACS | ID: lil-732507

RESUMEN

Associadas a projetos de construção da ideia de nação, no Brasil monárquico foram encaminhadas, pelo governo imperial, algumas iniciativas no sentido de materializar propostas de educação física. O objetivo deste artigo é investigar os sentidos e significados atribuídos ao tema na legislação e nos relatórios anuais do Ministério dos Negócios do Império (1831-1889), com especial interesse pelo que se refere ao Rio de Janeiro. A abordagem do assunto nas fontes pesquisadas evidencia que as visões sobre a educação física se deram a partir de uma matriz que articulava concepções de moral, saúde e civilização, tendo que lidar com as condições concretas de um país recém-independente, periférico e com uma burocracia ainda em formação.


In association with its nation building projects, the imperial government in Brazil under monarchic rule took some concrete actions based on proposals for physical education. The aim of this article is to investigate the meanings and significations attributed to this subject in the legislation and the annual reports issued by the Ministry of Business of the Empire (1831-1889), giving special attention to Rio de Janeiro. The approach to the subject in the sources researched demonstrates that the views of physical education took shape through a web of ideas that associated moral, health and civilization conceptions, in a bid to deal with the concrete circumstances of a newly independent peripheral nation with a bureaucratic structure in the process of formation.


Asunto(s)
Animales , Femenino , Ratones , Carcinoma Pulmonar de Lewis/secundario , Catepsina B/antagonistas & inhibidores , Catepsinas/antagonistas & inhibidores , Endopeptidasas , Leucina/análogos & derivados , Neoplasias Hepáticas Experimentales/prevención & control , Neoplasias Hepáticas Experimentales/secundario , Invasividad Neoplásica/prevención & control , Catepsina L , Colágeno , Cisteína Endopeptidasas , Carcinoma Pulmonar de Lewis/metabolismo , Combinación de Medicamentos , Ensayos de Selección de Medicamentos Antitumorales , Laminina , Leucina/farmacocinética , Leucina/farmacología , Neoplasias Hepáticas Experimentales/enzimología , Proteoglicanos , Células Tumorales Cultivadas
2.
Braz. j. med. biol. res ; 43(3): 242-248, Mar. 2010. graf, tab
Artículo en Inglés | LILACS | ID: lil-539721

RESUMEN

The chemopreventive potential of water extracts of the Brassica vegetables cabbage and kale was evaluated by administering their aqueous extracts in drinking water ad libitum to Wistar rats submitted to Ito’s hepatocarcinogenesis model (CB group and K group, respectively - 14 rats per group). Animals submitted to this same model and treated with water were used as controls (W group - 15 rats). Treatment with the vegetable extracts did not inhibit (P > 0.05) placental glutathione S-transferase-positive preneoplastic lesions (PNL). The number of apoptotic bodies did not differ (P > 0.05) among the experimental groups. Ex vivo hydrogen peroxide treatment of rat livers resulted in lower (P < 0.05) DNA strand breakage in cabbage- (107.6 ± 7.8 µm) and kale- (110.8 ± 10.0 µm) treated animals compared with control (120.9 ± 12.7 µm), as evaluated by the single cell gel (comet) assay. Treatment with cabbage (2 ± 0.3 µg/g) or kale (4 ± 0.2 µg/g) resulted in increased (P < 0.05) hepatic lutein concentration compared with control (0.5 ± 0.07 µg/g). Despite the absence of inhibitory effects of cabbage and kale aqueous extracts on PNL, these Brassica vegetables presented protection against DNA damage, an effect possibly related to increased hepatic lutein concentrations. However, it must be pointed out that the cause-effect relationship between lutein levels and protection is hypothetical and remains to be demonstrated.


Asunto(s)
Animales , Masculino , Ratas , Antioxidantes/farmacología , Brassica/química , Daño del ADN , Neoplasias Hepáticas Experimentales/prevención & control , Extractos Vegetales/farmacología , Lesiones Precancerosas/prevención & control , Anticarcinógenos/farmacología , Apoptosis/efectos de los fármacos , ADN , Glutatión Transferasa/análisis , Neoplasias Hepáticas Experimentales/inducido químicamente , Neoplasias Hepáticas Experimentales/enzimología , Lesiones Precancerosas/inducido químicamente , Lesiones Precancerosas/enzimología , Ratas Wistar
3.
Arq. gastroenterol ; 43(2): 121-124, abr. -jun. 2006.
Artículo en Portugués | LILACS | ID: lil-435256

RESUMEN

RACIONAL: O fenobarbital é utilizado em modelos experimentais não só por ser um importante agente promotor da carcinogênese em fígado de ratos, como também por ser não-genotóxico, órgão-específico e dose-dependente. OBJETIVOS: Avaliar o efeito da administração diária de fenobarbital em ratos, desde o nascimento até os 24 meses de idade, na ausência concomitante de administração de agentes químicos iniciadores da carcinogênese. MATERIAL E MÉTODOS: Um grupo controle de ratos machos Wistar recebeu dieta básica e a esta, do outro grupo, foi adicionado diariamente, fenobarbital a 0,05 por cento, durante 24 meses. Cortes dos lobos médio e direito do fígado foram submetidos ao processamento histológico e corados pela hematoxilina-eosina e coloração imunoistoquímica para a glutationa S-transferase forma placentária. RESULTADOS: Detectaram-se áreas glutationa S-transferase forma placentária positivas em ambos os grupos e as imagens foram analisadas quanto ao número e à extensão da superfície, mediante análise de imagem por histomorfometria. CONCLUSÃO: O uso crônico de fenobarbital não alterou o número de áreas glutationa S-transferase forma placentária positivas, havendo, no entanto, aumento no tamanho médio de áreas glutationa S-transferase forma placentária positivas, com conseqüente aumento da superfície glutationa S-transferase forma placentária positiva, sendo este aumento provavelmente relacionado a maior capacidade evolutiva dessas lesões e possível irreversibilidade das mesmas.


BACKGROUND: Phenobarbital has been used in experimental models because it is an important agent of carcinogenesis promotion in the liver of rats, and it is also non-genotoxic, organ-specific and dose-dependent. AIM: To evaluate the effects of the daily administration of phenobarbital in old rats treated with phenobarbital since their birth up to 24 months of age, in the absence of concomitant administration of chemical agents, which initiate carcinogenesis. PATIENTS AND METHODS: A control group of male Wistar rats was fed with a basic diet and a second group was fed with the same basic diet added of 0.05 percent of phenobarbital, for a period of 24 months. Medium and right liver fragments were submitted to the histological processing and they were stained by hematoxiciline and eosin and were immunohystochemically colored to glutathione S-transferase placentary form. RESULTS: Glutathione S-transferase placentary positive zones were detected in both groups and the images were analyzed concerning their number and surface extension through the technique of histometry analyses. CONCLUSION: Chronic use of phenobarbital did not modify the number of glutathione S-transferase placentary form positive areas. Although, data indicates that glutathione S-transferase placentary form positive areas media size are increased, probably because there are an increase in their evolution capacity and irreversibility.


Asunto(s)
Animales , Masculino , Ratas , Glutatión Transferasa/metabolismo , Neoplasias Hepáticas Experimentales/enzimología , Fenobarbital/farmacología , Inmunohistoquímica , Neoplasias Hepáticas Experimentales/inducido químicamente , Neoplasias Hepáticas Experimentales/patología , Lesiones Precancerosas/enzimología , Ratas Wistar
4.
Experimental & Molecular Medicine ; : 493-498, 2004.
Artículo en Inglés | WPRIM | ID: wpr-226071

RESUMEN

Hydroxyurea is commonly used to treat hematologic disorders and some type of solid tumors, but the mechanism for its therapeutic effect is not clearly known. In this study, we examined the effect of hydroxyurea on rat hepatoma McA-RH7777 cells, specifically, on the role of mitogen-activated protein (MAP) kinase signal transduction pathways and p21Waf1, p27Kip1 and p53. Rat hepatoma McA-RH7777 cells treated with hydroxyurea for 7 days, caused the inhibition of cell growth in a dose-dependent manner. But, this growth inhibition was not caused by necrosis or apoptosis but instead was associated with cell senescence-like change as evidenced by senescence associated-beta-galactosidase staining, and cells arrest at G1 phase of cell cycle. Phosphorylation of MAP kinases, such as ERK, JNK, and p38, was found to be decreased after treatment of cells with hydroxyurea. But, the expression of p21Waf1 was increased, while p27Kip1 and p53 were not detected in hydroxyurea treated rat hepatoma cells. Hydroxyurea treatment induced G1 arrest and a senescence-like changes in rat hepatoma McA-RH7777 cells may be the likely results of signal disruption of MAP kinases (ERK, JNK, and p38 MAP kinase) and p21Waf1 over-expression.


Asunto(s)
Animales , Ratas , Antineoplásicos/farmacología , Senescencia Celular/efectos de los fármacos , Proteínas de Ciclo Celular/análisis , Línea Celular Tumoral , Proliferación Celular/efectos de los fármacos , Fase G1/efectos de los fármacos , Hidroxiurea/farmacología , Neoplasias Hepáticas Experimentales/enzimología , Proteínas Quinasas Activadas por Mitógenos/análisis , Fosforilación/efectos de los fármacos , Proteína p53 Supresora de Tumor/análisis , Proteínas Supresoras de Tumor/análisis , Regulación hacia Arriba
5.
Genet. mol. res. (Online) ; 2(3): 295-308, Sept. 2003.
Artículo en Inglés | LILACS | ID: lil-417600

RESUMEN

The effects of crude extracts of the mushroom Agaricus blazei Murrill (Agaricaceae) on both DNA damage and placental form glutathione S-transferase (GST-P)-positive liver foci induced by diethylnitrosamine (DEN) were investigated. Six groups of adult male Wistar rats were used. For two weeks, animals of groups 3 to 6 were treated with three aqueous solutions of A. blazei (mean dry weight of solids being 1.2, 5.6, 11.5 and 11.5 mg/ml, respectively). After this period, groups 2 to 5 were given a single ip injection 200 mg/kg DEN and groups 1 and 6 were treated with 0.9 NaCl. All animals were subjected to 70 partial hepatectomy at week five and sacrificed 4, 24 and 48 h or 8 weeks after DEN or 0.9 NaCl treatments (10th week after the beginning of the experiment). The alkaline comet assay and GST-P-positive liver foci development were used to evaluate the influence of the mushroom extracts on liver cell DNA damage and on the initiation of liver carcinogenesis, respectively. Previous treatment with the highest concentration of A. blazei (11.5 mg/ml) significantly reduced DNA damage, indicating a protective effect against DEN-induced liver cytotoxicity/genotoxicity. However, the same dose of mushroom extract significantly increased the number of GST-P-positive liver foci


Asunto(s)
Animales , Masculino , Agaricus/química , Anticarcinógenos/farmacología , Daño del ADN/efectos de los fármacos , Glutatión Transferasa/efectos de los fármacos , Neoplasias Hepáticas Experimentales/prevención & control , Carcinógenos , Ensayo Cometa , Dietilnitrosamina , Ensayos de Selección de Medicamentos Antitumorales , Hígado/efectos de los fármacos , Hígado/enzimología , Hígado/patología , Glutatión Transferasa/análisis , Neoplasias Hepáticas Experimentales/inducido químicamente , Neoplasias Hepáticas Experimentales/enzimología , Ratas , Ratas Wistar
6.
Journal of Korean Medical Science ; : 183-188, 1995.
Artículo en Inglés | WPRIM | ID: wpr-7336

RESUMEN

Transferrin receptor (TR) performs the major function of binding and internalizing its specific iron-loaded ligand, transferrin, and its expression is closely linked to the proliferation status of the cell. This study was undertaken to elucidate TR expression in the hyperplastic lesion of hepatocyte in chemically induced hepatic carcinogenesis. The resistant hepatocyte model was chosen for a rat model of carcinogenesis and Sprague-Dawley rats were divided into the following groups: the control groups of normal diet and iron-rich diet with or without hydroxyquinoline and the groups of carcinogen alone and carcinogen plus iron-rich diet with or without administration of hydroxyquinoline. Microscopic changes in the liver, expression of transferrin receptor and glucose-6-phosphatase were studied. The hepatocyte of the control group showed both cytoplasmic and membranous expression of TR. The liver of rats fed on high iron diet accumulated iron and the expression of TR was down regulated by intrahepatic iron accumulation. In the carcinogen administered group the resistant hepatocyte of hyperplastic lesion revealed strong membranous expression of TR and failed to accumulate iron in spite of high iron diet but in contrast the surrounding non-resistant hepatocyte expressed TR in both the membrane and cytoplasm and stored iron when fed on high iron diet. The strong membranous expression of TR is one of the characteristics of the resistant hepatocyte of hyperplastic lesion and it seems to be related to the inability to accumulate iron in spite of a high iron diet.


Asunto(s)
Masculino , Ratas , Animales , Glucosa-6-Fosfatasa/metabolismo , Inmunohistoquímica , Hierro/análisis , Hígado/química , Neoplasias Hepáticas Experimentales/enzimología , Ratas Sprague-Dawley , Receptores de Transferrina/biosíntesis
7.
Yonsei Medical Journal ; : 37-48, 1988.
Artículo en Inglés | WPRIM | ID: wpr-20078

RESUMEN

r-Glutamyltranspeptidase (r-GT) from a rat hepatoma induced by 3'-methyl-4-dimethylaminoazobenzene (3'-Me DAB) was purified 833 fold. The purified enzyme had a specific activity of 15.0 U/mg protein with an overall yield of 3.8%. The molecular weight of native r-GT was estimated as about 350,000 daltons, whichs a multicomplex of a single polypetide having a M W of 59,000. Anti r-GT rabbit antiserum cross-reacted with kidney r-GT as well as liver r-GT. Tryptic digestion of r-GT followed by separation with Con A sepharose column chromatography resulted in two major glycopeptides. A tumor associated antigen was prepared by the conjugation of a tryptic glycopeptide of r-GT to keyhole limpets hemocyanin and an antibody against this antigen cross-reacted preferentially with r-GT in rat hepatoma tissue.


Asunto(s)
Masculino , Ratas , Animales , Antígenos de Neoplasias/aislamiento & purificación , Neoplasias Hepáticas Experimentales/enzimología , Peso Molecular , gamma-Glutamiltransferasa/inmunología
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