Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 4 de 4
Filtrar
Mais filtros











Intervalo de ano de publicação
1.
Int. arch. otorhinolaryngol. (Impr.) ; 19(1): 93-95, Jan-Mar/2015. graf
Artigo em Inglês | LILACS | ID: lil-741535

RESUMO

Introduction Schwannoma of the olfactory groove is an extremely rare tumor that can share a differential diagnosis with meningioma or neuroblastoma. Objectives The authors present a case of giant schwannoma involving the anterior cranial fossa and ethmoid sinuses. Case Report The patient presented with a 30-month history of left nasal obstruction, anosmia, and sporadic ipsilateral bleeding. Computed tomography of the paranasal sinuses revealed expansive lesion on the left nasal cavity extending to nasopharynx up to ethmoid and sphenoid sinuses bilaterally with intraorbital and parasellar extension to the skull base. Magnetic resonance imaging scan confirmed the expansive tumor without dural penetration. Biopsy revealed no evidence of malignancy and probable neural cell. Bifrontal craniotomy was performed combined with lateral rhinotomy (Weber-Ferguson approach), and the lesion was totally removed. The tumor measured 8.0 4.3 3.7 cm and microscopically appeared as a schwannoma composed of interwoven bundles of elongated cells (Antoni A regions)mixed with less cellular regions (Antoni B). Immunohistochemical study stained intensively for vimentin and S-100. Conclusion Schwannomas of the olfactory groove are extremely rare, and the findings of origin of this tumor is still uncertain but recent studies point most probably to the meningeal branches of trigeminal nerve or anterior ethmoidal nerves. .


Assuntos
Animais , Feminino , Masculino , Camundongos , Permeabilidade da Membrana Celular/fisiologia , Células Ciliadas Auditivas/fisiologia , Canais Iônicos/fisiologia , Mecanotransdução Celular/fisiologia , Animais Recém-Nascidos , Caderinas/genética , Permeabilidade da Membrana Celular/genética , Quelantes/farmacologia , Sulfato de Di-Hidroestreptomicina/farmacologia , Embrião de Mamíferos , Ácido Egtázico/análogos & derivados , Ácido Egtázico/farmacologia , Células Ciliadas Auditivas/citologia , Células Ciliadas Auditivas/efeitos dos fármacos , Técnicas In Vitro , Canais Iônicos/efeitos dos fármacos , Camundongos Transgênicos , Mecanotransdução Celular/efeitos dos fármacos , Mecanotransdução Celular/genética , Potenciais da Membrana/efeitos dos fármacos , Potenciais da Membrana/genética , Miosinas/genética , Órgão Espiral/citologia , Precursores de Proteínas/genética
2.
Biochim Biophys Acta ; 1418(1): 147-57, 1999 Apr 14.
Artigo em Inglês | MEDLINE | ID: mdl-10209219

RESUMO

Potassium efflux in yeast induced by several cationic compounds showed different characteristics. All of the observed efflux required glucose as substrate at the concentrations used. For most of them, the phenomenon required binding of the cationic compound to the cell surface and increased with the negative cell surface charge, and for all the compounds tested, it depended on a metabolizable substrate. Efflux induced with terbium chloride appeared more likely due to the function of a K+/H+ antiporter. With DEAE-dextran and dihydrostreptomycin, potassium efflux was dependent on the cell potassium content and was also sensitive to osmotic changes of the medium. DEAE-dextran-provoked efflux was not due to cell disruption. Dihydrostreptomycin seemed to activate a potassium efflux system which could not be studied in isolation, but its inhibition of potassium uptake may also be involved. Except for cells treated with ethidium bromide, no appreciable cell disruption was observed. The potassium efflux observed appears to be a membrane phenomenon reversible after washing with magnesium chloride.


Assuntos
Canais de Potássio/metabolismo , Saccharomyces cerevisiae/metabolismo , Antiporters/metabolismo , DEAE-Dextrano/farmacologia , Sulfato de Di-Hidroestreptomicina/farmacologia , Concentração de Íons de Hidrogênio , Cloreto de Magnésio , Pressão Osmótica , Antiportadores de Potássio-Hidrogênio , Sorbitol/farmacologia , Térbio/farmacologia
3.
Antimicrob Agents Chemother ; 31(10): 1627-31, 1987 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-2449121

RESUMO

Incubation of streptomycin-resistant (rpsL) mutants of Salmonella typhimurium in alkaline nutrient medium containing streptomycin brought about an inhibition of cell growth that was readily reversed by removing the antibiotic or neutralizing the medium. Growth inhibition was maximal at pH 8.2 and a streptomycin concentration of 800 micrograms/ml. A similar amount of dihydrostreptomycin had a negligible effect, and 10-times-higher concentrations of this antibiotic were required to reproduce the streptomycin action. Addition of streptomycin (400 micrograms/ml) to rpsL cells in alkaline (pH 8.2) nutrient medium caused inhibition of protein and DNA synthesis and also, but to a lower degree, of RNA synthesis. This effect on macromolecular synthesis was not due to ATP deprivation, since ATP content rose after addition of the antibiotic. At pH 8.2, the rate of entrance of streptomycin increased fourfold with respect to the rate at pH 7.0, leading to a large accumulation of streptomycin into rpsL cells. Uptake of the antibiotic was halted by addition of KCN or chloramphenicol. Equal uptake was obtained with 800 micrograms of dihydrostreptomycin or 400 micrograms of streptomycin per ml, yet the former did not affect cell growth at that concentration. It is concluded that high pH stimulates streptomycin and dihydrostreptomycin uptake by rpsL strains but only streptomycin accumulation causes growth inhibition in cells lacking the high-affinity ribosomal site.


Assuntos
Salmonella typhimurium/efeitos dos fármacos , Estreptomicina/farmacologia , Trifosfato de Adenosina/metabolismo , Proteínas de Bactérias/biossíntese , Meios de Cultura , DNA Bacteriano/biossíntese , Sulfato de Di-Hidroestreptomicina/síntese química , Sulfato de Di-Hidroestreptomicina/metabolismo , Sulfato de Di-Hidroestreptomicina/farmacologia , Resistência Microbiana a Medicamentos , Concentração de Íons de Hidrogênio , Mutação , Consumo de Oxigênio/efeitos dos fármacos , RNA Bacteriano/biossíntese , Salmonella typhimurium/genética , Estreptomicina/metabolismo
SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA