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1.
Genome Announc ; 5(8)2017 Feb 23.
Artigo em Inglês | MEDLINE | ID: mdl-28232448

RESUMO

Here, we present the complete genome sequences of two Zika virus (ZIKV) strains, EcEs062_16 and EcEs089_16, isolated from the sera of febrile patients in Esmeraldas City, in the northern coastal province of Esmeraldas, Ecuador, in April 2016. These are the first complete ZIKV genomes to be reported from Ecuador.

2.
J Neural Transm (Vienna) ; 119(10): 1085-96, 2012 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-22798027

RESUMO

The natural rotation of the earth generates an environmental day-night cycle that repeats every 24 h. This daily transition from dawn to dusk provides one of the most important time cues to which the majority of organisms synchronise their activity. Under these conditions, natural light, a photic stimulus, provides the principal entraining cue. In mammals, an endogenous circadian pacemaker located within the suprachiasmatic nucleus (SCN) of the hypothalamus acts as a coordinating centre to align physiological activity with the environmental light-dark cycle. However, the SCN also receives regulatory input from a number of behavioural, non-photic, cues such as physical activity, social interactions and feeding routines. The unique ability of the SCN to integrate both photic and non-photic cues allows it to generate a rhythm that is tailored to the individual and entrained to the environment. Here, we review the key neurotransmitter systems involved in both photic and non-photic transmission to the SCN and their interactions that assist in generating an entrained output rhythm. We also consider the impact on health of a desynchronised circadian system with a focus on depressive affective disorders and current therapies aimed at manipulating the relationship between photic and non-photic SCN regulators.


Assuntos
Ritmo Circadiano/fisiologia , Depressão/fisiopatologia , Animais , Transtornos Cronobiológicos/complicações , Depressão/complicações , Depressão/patologia , Humanos , Vias Neurais/fisiopatologia , Estimulação Luminosa , Núcleo Supraquiasmático/fisiopatologia , Transmissão Sináptica/fisiologia
3.
Invest Ophthalmol Vis Sci ; 38(11): 2423-7, 1997 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-9344364

RESUMO

PURPOSE: Diabetic retinopathy and other diseases associated with retinal edema are characterized by increased microvascular leakage. Astrocytes have been proposed to maintain endothelial function in the brain, suggesting that glial impairment may underlie the development of retinal edema. The purpose of this study was to test the effects of astrocytes on barrier properties in retinal microvascular endothelial cells. METHODS: Bovine retinal microvascular endothelial cells were exposed to conditioned media from rat brain astrocytes. Transendothelial electrical resistance (TER) was determined on 24-mm Transwell (Cambridge, MA) polycarbonate filters with the End-Ohm device (World Precision Instruments, Sarasota, FL). ZO-1 protein content was quantified by microtiter enzyme-linked immunosorbent assay. RESULTS: Astrocyte-conditioned medium (ACM) significantly increased TER (P < 0.0001) and ZO-1 content (P < 0.01). Both serum-containing and serum-free N1B defined ACM increased ZO-1 expression, but heating abolished the effect. Serum-free ACM decreased cell proliferation by 16%. CONCLUSIONS: Astrocytes release soluble, heat-labile factors that increase barrier properties and tight junction protein content. These results suggest that astrocytes enhance blood-retinal barrier properties, at least in part by increasing tight junction protein expression. Our findings suggest that glial malfunction plays an important role in the pathogenesis of vasogenic retinal edema.


Assuntos
Astrócitos/fisiologia , Barreira Hematorretiniana/fisiologia , Endotélio Vascular/metabolismo , Proteínas de Membrana/biossíntese , Fosfoproteínas/biossíntese , Vasos Retinianos/metabolismo , Animais , Animais Recém-Nascidos , Bovinos , Divisão Celular , Células Cultivadas , Meios de Cultivo Condicionados , Condutividade Elétrica , Endotélio Vascular/citologia , Ensaio de Imunoadsorção Enzimática , Imuno-Histoquímica , Ratos , Junções Íntimas/fisiologia , Proteína da Zônula de Oclusão-1
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