Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 2 de 2
Filtrar
Mais filtros

Base de dados
Ano de publicação
Tipo de documento
Intervalo de ano de publicação
1.
Food Chem ; 345: 128778, 2021 May 30.
Artigo em Inglês | MEDLINE | ID: mdl-33310250

RESUMO

The innovative combination of ultrasound (Us) with a thermal exchanger to produce high quality extra virgin olive oil (EVOO) was studied using Nuclear Magnetic Resonance (NMR) spectroscopy and multivariate analysis (MVA). Major and minor metabolomic components of Apulian Coratina EVOO obtained using the two methods were compared. Early and late olive ripening stages were also considered. An increased amount of polyphenols was found for EVOOs obtained using the Us with respect to the conventional method for both early and late ripening stages (900.8 ± 10.3 and 571.9 ± 9.9 mg/kg versus 645.1 ± 9.3 and 440.8 ± 10.4 mg/kg). NMR spectroscopy showed a significant increase (P < 0.05) in polyunsaturated fatty acids (PUFA) as well as in the tyrosol and hydroxytyrosol derivatives, such as oleocanthal, oleacein, and elenolic acid, for both ripening stages. In conclusion, NMR spectroscopy provides information about the metabolomic components of EVOOs to producers, while the Us process increases the levels of healthy bioactive components.


Assuntos
Indústria Alimentícia , Espectroscopia de Ressonância Magnética , Metabolômica , Azeite de Oliva/metabolismo , Temperatura , Ondas Ultrassônicas , Análise Multivariada
2.
J Neurol Sci ; 343(1-2): 218-20, 2014 Aug 15.
Artigo em Inglês | MEDLINE | ID: mdl-24939576

RESUMO

Hereditary spastic paraplegia (HSP) includes a group of diseases characterized by progressive spastic weakness of the lower limbs (pure forms) with possible additional signs (complicated forms). The SPG10 form is due to alteration in the kinesin1A gene (KIF5A) that encodes the neuronal kinesin heavy chain, a protein required for the anterograde axonal transport. We performed clinical, neurophysiological and molecular studies in two siblings affected by AD-HSP complicated by deafness. The screening of the KIF5A gene revealed the novel mutation p.Leu259Gln in two affected siblings and in their father with a pure form of HSP.


Assuntos
Saúde da Família , Perda Auditiva Neurossensorial/genética , Cinesinas/genética , Mutação/genética , Paraparesia Espástica/genética , Adulto , Análise Mutacional de DNA , Feminino , Perda Auditiva Neurossensorial/complicações , Humanos , Itália , Masculino , Neurofisiologia , Paraparesia Espástica/complicações
SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA