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1.
J Med Genet ; 45(1): 29-31, 2008 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-17932121

RESUMO

Spinal muscular atrophy (SMA) is an inherited neuromuscular disorder caused by homozygous absence of the survival motor neuron gene (SMN1). All patients have at least one, usually two to four copies of the related SMN2 gene which, however, produce insufficient levels of functional SMN protein due to the exclusion of exon 7 in the majority of SMN2 transcripts. Here, we show that salbutamol, a beta2-adrenoceptor agonist, determines a rapid and significant increase in SMN2-full length mRNA and SMN protein in SMA fibroblasts, predominantly by promoting exon 7 inclusion in SMN2 transcripts. These data, together with previous clinical findings, provide a strong rationale to investigate further the clinical efficacy of salbutamol in SMA patients.


Assuntos
Agonistas Adrenérgicos beta/farmacologia , Albuterol/farmacologia , Proteína de Ligação ao Elemento de Resposta ao AMP Cíclico/metabolismo , Fibroblastos/efeitos dos fármacos , Regulação da Expressão Gênica , Proteínas do Tecido Nervoso/metabolismo , RNA Mensageiro/metabolismo , Proteínas de Ligação a RNA/metabolismo , Proteína de Ligação ao Elemento de Resposta ao AMP Cíclico/genética , Éxons/genética , Fibroblastos/metabolismo , Humanos , Atrofia Muscular Espinal/tratamento farmacológico , Atrofia Muscular Espinal/genética , Atrofia Muscular Espinal/metabolismo , Proteínas do Tecido Nervoso/genética , Splicing de RNA/efeitos dos fármacos , RNA Mensageiro/genética , Proteínas de Ligação a RNA/genética , Proteínas do Complexo SMN , Proteína 1 de Sobrevivência do Neurônio Motor , Proteína 2 de Sobrevivência do Neurônio Motor
2.
Neuromuscul Disord ; 17(5): 400-3, 2007 May.
Artigo em Inglês | MEDLINE | ID: mdl-17433677

RESUMO

Previous studies showed that SMN2 copy number correlates inversely with the disease severity. Our aim was to evaluate SMN2 copy numbers and the Hammersmith functional motor scale in 87 patients with SMA II in order to establish whether, within SMAII, the number of copies correlates with the severity of functional impairment. Our results showed a relative variability of functional scores, but a significant correlation between the number of SMN2 genes and the level of function.


Assuntos
Proteína de Ligação ao Elemento de Resposta ao AMP Cíclico/genética , Dosagem de Genes/genética , Proteínas do Tecido Nervoso/genética , Proteínas de Ligação a RNA/genética , Índice de Gravidade de Doença , Atrofias Musculares Espinais da Infância/genética , Criança , Pré-Escolar , Feminino , Humanos , Masculino , Proteínas do Complexo SMN , Atrofias Musculares Espinais da Infância/fisiopatologia , Estatística como Assunto , Proteína 2 de Sobrevivência do Neurônio Motor
3.
Neurology ; 68(1): 51-5, 2007 Jan 02.
Artigo em Inglês | MEDLINE | ID: mdl-17082463

RESUMO

OBJECTIVE: To assess the efficacy of phenylbutyrate (PB) in patients with spinal muscular atrophy in a randomized, double-blind, placebo-controlled trial involving 10 Italian centers. METHODS: One hundred seven children were assigned to receive PB (500 mg/kg/day) or matching placebo on an intermittent regimen (7 days on/7 days off) for 13 weeks. The Hammersmith functional motor scale (primary outcome measure), myometry, and forced vital capacity were assessed at baseline and at weeks 5 and 13. RESULTS: Between January and September 2004, 107 patients aged 30 to 154 months were enrolled. PB was well tolerated, with only one child withdrawing because of adverse events. Mean improvement in functional score was 0.60 in the PB arm and 0.73 in placebo arm (p = 0.70). Changes in the secondary endpoints were also similar in the two study arms. CONCLUSIONS: Phenylbutyrate was not effective at the regimen, schedule, and duration used in this study.


Assuntos
Atrofia Muscular Espinal/tratamento farmacológico , Fenilbutiratos/uso terapêutico , Criança , Pré-Escolar , Método Duplo-Cego , Feminino , Humanos , Masculino , Atrofia Muscular Espinal/epidemiologia , Atrofia Muscular Espinal/fisiopatologia , Estudos Retrospectivos
4.
J Appl Microbiol ; 92(5): 828-36, 2002.
Artigo em Inglês | MEDLINE | ID: mdl-11972685

RESUMO

AIMS: The persistent circulation of hepatitis A virus (HAV) in the Mediterranean area suggests the need for monitoring its presence in the environment. A reverse transcriptase-polymerase chain reaction (RT-PCR) was used to detect the presence of HAV in several consecutive raw sewage and final effluent samples, collected over an 8-month period from an activated sludge treatment plant in southern Italy. METHODS AND RESULTS: Two distinct purification protocols, either based on antigen-capture with monoclonal antibody (AC) or RNA extraction, were compared. The possible influence of the antibody used in the AC phase was evaluated in preliminary experiments on HAV-spiked samples, using two different monoclonal antibodies. Hepatitis A virus RNA was detected in all but one sewage environmental sample examined. The contemporary presence of enteroviruses, reoviruses and phages was observed, while HAV growth in cell culture was hampered. CONCLUSIONS: The RT-PCR technique was confirmed to be a valuable tool for the rapid monitoring of HAV in sewage samples. In addition, this study demonstrated that application of different sample purification methods can result in different levels of sensitivity of the assay and that, in the antigen-capture method, the choice of antibody can have a crucial role. SIGNIFICANCE AND IMPACT OF THE STUDY: This work underlines the need for technical uniformity in environmental studies from different laboratories for a correct and useful comparison of the results.


Assuntos
Vírus da Hepatite A/isolamento & purificação , Reação em Cadeia da Polimerase Via Transcriptase Reversa , Esgotos/microbiologia , Microbiologia da Água , Sequência de Aminoácidos , Animais , Anticorpos Monoclonais/imunologia , Antígenos Virais/química , Antígenos Virais/imunologia , Antígenos Virais/isolamento & purificação , Genoma Viral , Vírus da Hepatite A/química , Vírus da Hepatite A/genética , Humanos , Dados de Sequência Molecular , RNA Viral/análise , RNA Viral/isolamento & purificação , Sensibilidade e Especificidade , Análise de Sequência de DNA , Proteínas Virais/química
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