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1.
Acta Histochem ; 119(6): 632-637, 2017 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-28780960

RESUMO

The present study was designed to investigate the glucose transporter 8 (GLUT8) expression and localization in adult boar testis. Localization and expression of GLUT8 were conducted with Western Blotting, immunohistochemistry and reverse transcription-polymerase chain reaction (RT-PCR) methods GLUT8 protein and mRNA were expressed in the boar testes. The results of Western Blotting analysis showed specificity of the antibody for protein of boar testes. The immunohistochemistry results showed that GLUT8 protein mainly localized in spermatocytes, round spermatids and elongated spermatids of the seminiferous tubules in the adult boar testes. And the GLUT8 expression persists during eight stages of boar spermatogenesis. GLUT8 may mainly provide glucose for the later stage of germ cell differentiation in adluminal compartment in adult boar testes. These results suggested that GLUT8 is important for the spermatogenesis in the adult boar testes.


Assuntos
Regulação da Expressão Gênica no Desenvolvimento , Proteínas Facilitadoras de Transporte de Glucose/genética , Espermatogênese/genética , Testículo/metabolismo , Animais , Western Blotting , Proteínas Facilitadoras de Transporte de Glucose/metabolismo , Imuno-Histoquímica , Masculino , Reação em Cadeia da Polimerase , Espermátides/metabolismo , Suínos
2.
Pharm Biol ; 51(9): 1137-43, 2013 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-23607905

RESUMO

CONTEXT: The prevalence of infectious bursal disease has brought about enormous financial losses to the world poultry industry. Chinese herb medicines can provide valuable materials for discovery and development of new drugs. OBJECTIVE: To screen constituents derived from Chinese herb medicines for their antiviral activity against infectious bursal disease virus (IBDV) in vitro. MATERIALS AND METHODS: Twenty constituents derived from Chinese herb medicines and B87 strain of IBDV were used. The 50% cytotoxic concentration (CC50) and 50% effective concentration (EC50) were determined by visualization of cytopathologic effect (CPE) and 3-(4,5-dimethyithiazol-2-yl)-2,5-diphenyltetrazoliumbromide (MTT) test on chicken embryo fibroblast. Selectivity index (SI) and inhibition ratio (%I) were calculated from the data obtained from the MTT test. RESULTS: Antiviral assays showed dipotassium glycyrrhizinate and ligustrazine hydrochloride among the 20 constituents tested exhibited significant inhibitory activity against IBDV in a dose-dependent manner. EC50 of dipotassium glycyrrhizinate and ligustrazine hydrochloride were 663.2 ± 268.4 and 92.52 ± 21.13 µg/mL, and SI were >4.52 and >21.62, respectively. The time-of-addition and virucidal assay indicated that anti-IBDV activity of the two constituents could be due to their inhibiting virus replication and/or inactivating virus directly. The inhibition of virus attachment was not observed in the adsorption inhibition assay. Dipotassium glycyrrhizinate and ligustrazine hydrochloride exhibited more than 70% and 80% inhibition of IBDV, respectively, at the maximum safe concentration. DISCUSSION AND CONCLUSION: We believe that dipotassium glycyrrhizinate and ligustrazine hydrochloride can be used to develop a new anti-IBDV compound, and it is worth applying the constituents in clinical practice.


Assuntos
Antivirais/farmacologia , Descoberta de Drogas , Medicamentos de Ervas Chinesas/química , Vírus da Doença Infecciosa da Bursa/efeitos dos fármacos , Animais , Antivirais/efeitos adversos , Células Cultivadas , Embrião de Galinha , Fibroblastos/citologia , Fibroblastos/efeitos dos fármacos , Fibroblastos/virologia , Ácido Glicirrízico/efeitos adversos , Ácido Glicirrízico/farmacologia , Vírus da Doença Infecciosa da Bursa/crescimento & desenvolvimento , Concentração Inibidora 50 , Cinética , Testes de Sensibilidade Microbiana , Viabilidade Microbiana/efeitos dos fármacos , Pirazinas/efeitos adversos , Pirazinas/farmacologia , Replicação Viral/efeitos dos fármacos
3.
J Asian Nat Prod Res ; 14(8): 721-8, 2012.
Artigo em Inglês | MEDLINE | ID: mdl-22575045

RESUMO

This experiment was conducted to study the antiviral activities of sodium tanshinone IIA sulfonate (STS) against porcine reproductive and respiratory syndrome virus (PRRSV) and its mechanism. Anti-PRRSV activities of STS were observed on Marc-145 cells by using visualization of cytopathologic effect assay and 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) test, and its antiviral mechanism was determined by time-of-addition assay, adsorption inhibition assay, and virucidal assay. The results showed that STS could reduce the damage of PRRSV to Marc-145 cells, with the inhibition ratio exceeding to 100%, at the maximum non-cytotoxic concentration. The time-of-addition and virucidal assays indicated that the anti-PRRSV activities of STS could be due to inhibiting the virus replication or/and inactivating the virus directly. The inhibition of the virus attachment was not discovered in adsorption inhibition assay. The results proved that STS had strong anti-PRRSV activity and encouraged for further exploration of STS.


Assuntos
Antivirais/isolamento & purificação , Antivirais/farmacologia , Fenantrenos/farmacologia , Vírus da Síndrome Respiratória e Reprodutiva Suína/efeitos dos fármacos , Animais , Antivirais/química , Humanos , Estrutura Molecular , Fenantrenos/química , Sódio/farmacologia , Suínos
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