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1.
Sleep ; 41(9)2018 09 01.
Artículo en Inglés | MEDLINE | ID: mdl-29860401

RESUMEN

Study Objectives: Sleep is a reliable indicator of cognitive health in older individuals. Sleep spindles (SS) are non-rapid eye movement (NREM) sleep oscillations implicated in sleep-dependent learning. Their generation imply a complex activation of the thalamo-cortico-thalamic loop. Since SS require neuronal synchrony, the integrity of the white matter (WM) underlying these connections is of major importance. During aging, both SS and WM undergo important changes. The goal of this study was to investigate whether WM integrity could predict the age-related reductions in SS characteristics. Methods: Thirty young and 31 older participants underwent a night of polysomnographic recording and a 3T magnetic resonance imaging acquisition including a diffusion sequence. SS were detected in NREM sleep and EEG spectral analysis was performed for the sigma frequency band. WM diffusion metrics were computed in a voxelwise design of analysis. Results: Compared to young participants, older individuals showed lower SS density, amplitude, and sigma power. Diffusion metrics were correlated with SS amplitude and sigma power in tracts connecting the thalamus to the frontal cortex for the young but not for the older group, suggesting a moderation effect. Moderation analyses showed that diffusion metrics explained between 14% and 39% of SS amplitude and sigma power variance in the young participants only. Conclusion: Our results indicate that WM underlying the thalamo-cortico-thalamic loop predicts SS characteristics in young individuals, but does not explain age-related changes in SS. Other neurophysiological factors could better explain the effect of age on SS characteristics.


Asunto(s)
Envejecimiento/fisiología , Fases del Sueño/fisiología , Sustancia Blanca/diagnóstico por imagen , Sustancia Blanca/fisiología , Adulto , Factores de Edad , Anciano , Corteza Cerebral/diagnóstico por imagen , Corteza Cerebral/fisiología , Electroencefalografía/métodos , Femenino , Humanos , Imagen por Resonancia Magnética/métodos , Masculino , Persona de Mediana Edad , Polisomnografía/métodos , Tálamo/diagnóstico por imagen , Tálamo/fisiología , Adulto Joven
2.
Sleep ; 39(3): 613-24, 2016 Mar 01.
Artículo en Inglés | MEDLINE | ID: mdl-26612390

RESUMEN

STUDY OBJECTIVES: Optimal sleep is ensured by the interaction of circadian and homeostatic processes. Although synaptic plasticity seems to contribute to both processes, the specific players involved are not well understood. The EphA4 tyrosine kinase receptor is a cell adhesion protein regulating synaptic plasticity. We investigated the role of EphA4 in sleep regulation using electrocorticography in mice lacking EphA4 and gene expression measurements. METHODS: EphA4 knockout (KO) mice, Clock(Δ19/Δ19) mutant mice and littermates, C57BL/6J and CD-1 mice, and Sprague-Dawley rats were studied under a 12 h light: 12 h dark cycle, under undisturbed conditions or 6 h sleep deprivation (SLD), and submitted to a 48 h electrophysiological recording and/or brain sampling at different time of day. RESULTS: EphA4 KO mice showed less rapid eye movement sleep (REMS), enhanced duration of individual bouts of wakefulness and nonrapid eye movement sleep (NREMS) during the light period, and a blunted daily rhythm of NREMS sigma activity. The NREMS delta activity response to SLD was unchanged in EphA4 KO mice. However, SLD increased EphA4 expression in the thalamic/hypothalamic region in C57BL/6J mice. We further show the presence of E-boxes in the promoter region of EphA4, a lower expression of EphA4 in Clock mutant mice, a rhythmic expression of EphA4 ligands in several brain areas, expression of EphA4 in the suprachiasmatic nuclei of the hypothalamus (SCN), and finally an unchanged number of cells expressing Vip, Grp and Avp in the SCN of EphA4 KO mice. CONCLUSIONS: Our results suggest that EphA4 is involved in circadian sleep regulation.


Asunto(s)
Ritmo Circadiano/fisiología , Receptor EphA4/metabolismo , Privación de Sueño/fisiopatología , Sueño/fisiología , Animales , Proteínas CLOCK/genética , Ritmo Circadiano/genética , Oscuridad , Electrocorticografía , Fenómenos Electrofisiológicos , Homeostasis , Luz , Ratones , Ratones Endogámicos C57BL , Ratones Noqueados , Plasticidad Neuronal , Regiones Promotoras Genéticas/genética , Ratas , Ratas Sprague-Dawley , Receptor EphA4/biosíntesis , Receptor EphA4/deficiencia , Receptor EphA4/genética , Sueño/genética , Privación de Sueño/genética , Sueño REM/genética , Sueño REM/fisiología , Núcleo Supraquiasmático/metabolismo , Tálamo/metabolismo , Factores de Tiempo , Vigilia/genética , Vigilia/fisiología
3.
J Cutan Med Surg ; 12(1): 27-30, 2008.
Artículo en Inglés | MEDLINE | ID: mdl-18258154

RESUMEN

BACKGROUND: Soy lecithin is widely used as an emulsifier, not only in topical skin care products but also in various drugs administered either topically, orally, or intravenously or by inhalation. Patients strongly allergic to soy and/or peanuts can develop an anaphylactic reaction when exposed to soy lecithin. METHOD: We report a 3-year-old asthmatic boy, allergic to peanuts, who was treated at the emergency department for an exacerbation of asthma following an upper respiratory tract infection. Within an hour after receiving the second of two inhalations of an ipratropium bromide (Atrovent) metered dose inhaler, he developed respiratory distress and generalized urticaria, an adverse event that regressed within 48 hours of withdrawal of the suspected drug. Soy lecithin, contained as an excipient in the metered dose inhaler, was strongly suspected of being responsible for this reaction. CONCLUSION: Drug products containing soy lecithin can cause severe allergic reactions in patients allergic to peanuts or soy. Physicians should be aware that adverse drug reactions can be due to both the active medical component and the excipient ingredients.


Asunto(s)
Asma/tratamiento farmacológico , Broncodilatadores/química , Hipersensibilidad Inmediata/etiología , Hipersensibilidad Inmediata/inmunología , Ipratropio/química , Lecitinas/inmunología , Proteínas de Soja/inmunología , Arachis/inmunología , Asma/inmunología , Broncodilatadores/administración & dosificación , Broncodilatadores/efectos adversos , Preescolar , Excipientes , Hipersensibilidad a los Alimentos/etiología , Hipersensibilidad a los Alimentos/inmunología , Humanos , Ipratropio/administración & dosificación , Ipratropio/efectos adversos , Lecitinas/administración & dosificación , Lecitinas/efectos adversos , Masculino , Nebulizadores y Vaporizadores , Proteínas de Soja/administración & dosificación , Proteínas de Soja/efectos adversos
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