Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 3 de 3
Filtrar
Mais filtros










Base de dados
Intervalo de ano de publicação
1.
J Cereb Blood Flow Metab ; 39(10): 2089-2095, 2019 10.
Artigo em Inglês | MEDLINE | ID: mdl-29862863

RESUMO

KIR6.1 (KCNJ8) is a subunit of ATP sensitive potassium channel (KATP) that plays an important role in the control of peripheral vascular tone and is highly expressed in brain contractile cells (vascular smooth muscle cells and pericytes). This study determined the effect of global deletion of the KIR6.1 subunit on cerebral blood flow, neurovascular coupling and cerebral oxygenation in mice. In KIR6.1 deficient mice resting cerebral blood flow and brain parenchymal partial pressure of oxygen (PO2) were found to be markedly lower compared to that in their wildtype littermates. However, cortical blood oxygen level dependent responses triggered by visual stimuli were not affected in conditions of KIR6.1 deficiency. These data suggest that KATP channels containing KIR6.1 subunit are critically important for the maintenance of normal cerebral perfusion and parenchymal PO2 but play no significant role in the mechanisms underlying functional changes in brain blood flow.


Assuntos
Encéfalo/metabolismo , Circulação Cerebrovascular , Canais KATP/metabolismo , Oxigênio/metabolismo , Trifosfato de Adenosina/metabolismo , Animais , Encéfalo/irrigação sanguínea , Masculino , Camundongos , Oxigênio/sangue
2.
Neuroimage ; 139: 337-345, 2016 Oct 01.
Artigo em Inglês | MEDLINE | ID: mdl-27296012

RESUMO

The use of functional magnetic resonance imaging (fMRI) in mice is increasingly prevalent, providing a means to non-invasively characterise functional abnormalities associated with genetic models of human diseases. The predominant stimulus used in task-based fMRI in the mouse is electrical stimulation of the paw. Task-based fMRI in mice using visual stimuli remains underexplored, despite visual stimuli being common in human fMRI studies. In this study, we map the mouse brain visual system with BOLD measurements at 9.4T using flashing light stimuli with medetomidine anaesthesia. BOLD responses were observed in the lateral geniculate nucleus, the superior colliculus and the primary visual area of the cortex, and were modulated by the flashing frequency, diffuse vs focussed light and stimulus context. Negative BOLD responses were measured in the visual cortex at 10Hz flashing frequency; but turned positive below 5Hz. In addition, the use of interleaved snapshot GE-EPI improved fMRI image quality without diminishing the temporal contrast-noise-ratio. Taken together, this work demonstrates a novel methodological protocol in which the mouse brain visual system can be non-invasively investigated using BOLD fMRI.


Assuntos
Mapeamento Encefálico/métodos , Encéfalo/fisiologia , Vias Visuais/fisiologia , Percepção Visual/fisiologia , Animais , Feminino , Corpos Geniculados/fisiologia , Processamento de Imagem Assistida por Computador , Imageamento por Ressonância Magnética , Camundongos Endogâmicos C57BL , Estimulação Luminosa , Processamento de Sinais Assistido por Computador , Colículos Superiores/fisiologia , Córtex Visual/fisiologia
3.
J Phys Chem Lett ; 6(15): 2881-7, 2015 Aug 06.
Artigo em Inglês | MEDLINE | ID: mdl-26267174

RESUMO

The gelation kinetics of silica nanoparticles is a central process in physical chemistry, yet it is not fully understood. Gelation times are measured to increase by over 4 orders of magnitude, simply changing the monovalent salt species from CsCl to LiCl. This striking effect has no microscopic explanation within current paradigms. The trend is consistent with the Hofmeister series, pointing to short-ranged solvation effects not included in the standard colloidal (DLVO) interaction potential. By implementing a simple form for short-range repulsion within a model that relates the gelation timescale to the colloidal interaction forces, we are able to explain the many orders of magnitude difference in the gelation times at fixed salt concentration. The model allows us to estimate the magnitude of the non-DLVO hydration forces, which dominate the interparticle interactions on the length scale of the hydrated ion diameter. This opens the possibility of finely tuning the gelation time scale of nanoparticles by just adjusting the background electrolyte species.

SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA
...