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1.
J Texture Stud ; 52(4): 470-479, 2021 08.
Artigo em Inglês | MEDLINE | ID: mdl-33999420

RESUMO

Crispness is one of the words most frequently used to describe the texture of fried or dried food in addition to being a key to the determination of freshness for many non-fried foods. In this study, a new feature value called the sum of variance was assessed for its contribution to the estimation of crispness. Dynamic time warping and its averaging algorithms were employed to determine the sum of variance from a set of sequential force data measured using an instrument. The sum of variance is a feature value that expresses the variance of multiple sequential data. In an experiment, seven chicken nugget samples were prepared, and five panels evaluated their texture according to six Japanese word descriptors. An instrument experiment determined the six feature values, including the sum of variance from the measurement data, whereas multiple linear regression was applied to determine the relationship between the sensory values and feature values. For three of the six textures, the sum of variance reduced the error between the sensory values and their estimated values by up to 50%, confirming that this feature contributes to the textural estimation of food crispness.


Assuntos
Galinhas , Manipulação de Alimentos , Animais , Alimentos , Fenômenos Mecânicos
2.
Brain Res ; 1490: 61-71, 2013 Jan 15.
Artigo em Inglês | MEDLINE | ID: mdl-23123209

RESUMO

Growth of neurite processes is a critical step in neuronal development, regeneration, differentiation, and response to injury. The discovery of compounds that can stimulate neurite formation would be important for developing new therapeutics against both neurodegenerative disorders and trauma-induced neuronal injuries. Semisynthetic derivatives of artemisinin, an active compound in Artemisia annua, have been effectively used in malaria treatment, but they have been shown to possess neurotoxic potential. In this study, we found unexpectedly that artemisinin and its derivatives induced neurite outgrowth of PC12 cells. Artemisinins containing an endoperoxide bridge such as artemisinin and dihydroartemisinin induced growth of neurite processes at concentrations that were slightly cytotoxic, artemisinin having the most potent maximal effect among them. Deoxyartemisinin, which lacks the endoperoxide bridge, was ineffective. Artemisinin-treated cells expressed increased levels of the neuronal marker ß(III)-tubulin. Artemisinin upregulated phosphorylation of extracellular signal-regulated kinase (ERK) and p38 mitogen-activated protein kinase (MAPK), critical signaling molecules in neuronal differentiation. Consistent with activation of the two MAPKs, neurite outgrowth induced by artemisinin was inhibited by the MAPK/ERK kinase inhibitor PD98059 and the p38 MAPK inhibitor SB203580. Artemisinin also induced phosphorylation of cyclic AMP response element-binding protein (CREB) that was almost completely attenuated by PD98059 but not by SB203580. Taken together, our results indicate that artemisinin and its derivatives containing the endoperoxide bridge induced differentiation of PC12 cells toward a neuronal phenotype and suggest that both activation of ERK signaling pathway, which leads to CREB phosphorylation, and activation of p38 MAPK signaling pathway are involved in this process.


Assuntos
Antimaláricos/farmacologia , Artemisininas/farmacologia , Sistema de Sinalização das MAP Quinases/efeitos dos fármacos , Neuritos/efeitos dos fármacos , Neuritos/fisiologia , Transdução de Sinais/efeitos dos fármacos , Proteínas Quinases p38 Ativadas por Mitógeno/efeitos dos fármacos , Animais , Western Blotting , Sobrevivência Celular/efeitos dos fármacos , Corantes , AMP Cíclico/metabolismo , Proteína de Ligação ao Elemento de Resposta ao AMP Cíclico/metabolismo , Interpretação Estatística de Dados , Proteínas Quinases Ativadas por Mitógeno/antagonistas & inibidores , Fator de Crescimento Neural/farmacologia , Células PC12 , Fosforilação , Ratos , Sais de Tetrazólio , Tiazóis , Proteínas Quinases p38 Ativadas por Mitógeno/antagonistas & inibidores
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