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1.
Proc Natl Acad Sci U S A ; 114(29): 7695-7700, 2017 07 18.
Artículo en Inglés | MEDLINE | ID: mdl-28674018

RESUMEN

Sudden infant death syndrome (SIDS), the leading cause of postneonatal infant mortality, likely comprises heterogeneous disorders with the common phenotype of sudden death without explanation upon postmortem investigation. Previously, we reported that ∼40% of SIDS deaths are associated with abnormalities in serotonin (5-hydroxytryptamine, 5-HT) in regions of the brainstem critical in homeostatic regulation. Here we tested the hypothesis that SIDS is associated with an alteration in serum 5-HT levels. Serum 5-HT, adjusted for postconceptional age, was significantly elevated (95%) in SIDS infants (n = 61) compared with autopsied controls (n = 15) [SIDS, 177.2 ± 15.1 (mean ± SE) ng/mL versus controls, 91.1 ± 30.6 ng/mL] (P = 0.014), as determined by ELISA. This increase was validated using high-performance liquid chromatography. Thirty-one percent (19/61) of SIDS cases had 5-HT levels greater than 2 SDs above the mean of the controls, thus defining a subset of SIDS cases with elevated 5-HT. There was no association between genotypes of the serotonin transporter promoter region polymorphism and serum 5-HT level. This study demonstrates that SIDS is associated with peripheral abnormalities in the 5-HT pathway. High serum 5-HT may serve as a potential forensic biomarker in autopsied infants with SIDS with serotonergic defects.


Asunto(s)
Asfixia/sangre , Biomarcadores/sangre , Serotonina/sangre , Muerte Súbita del Lactante/sangre , Adulto , Autopsia , Tronco Encefálico/metabolismo , Estudios de Casos y Controles , Cromatografía Líquida de Alta Presión , Estudios de Cohortes , Femenino , Genotipo , Humanos , Ácido Hidroxiindolacético/sangre , Lactante , Masculino , Polimorfismo Genético , Factores de Riesgo , Proteínas de Transporte de Serotonina en la Membrana Plasmática/genética
2.
Neurochem Res ; 39(9): 1640-7, 2014 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-25005622

RESUMEN

This review summarizes recent research on the potential cognitive and behavioural abnormalities induced by exposure to volatile anesthetics and suggests a role of hypoxia-inducible factor (HIF)-1α in mediating these events. Volatile anesthetics are widely utilized in clinical and research settings, yet the long-term safety of exposure to these agents is under debate. Findings from various animal models suggest volatile anesthetics induce widespread apoptosis in the central nervous system (CNS) that correlates with lasting deficits in learning and memory. Longitudinal analysis of clinical data highlight an increased risk of developmental disorders later in life when children are exposed to volatile anesthetics, particularly when exposures occur over multiple sessions. However, the mechanisms underlying these events have yet to be established. Considering the extensive use of volatile anesthetics, it is crucial that these events are better understood. The possible role of HIF-1α in volatile anesthetic-induced CNS abnormalities will be suggested and areas requiring urgent attention will be outlined.


Asunto(s)
Anestésicos por Inhalación/farmacología , Sistema Nervioso Central/lesiones , Subunidad alfa del Factor 1 Inducible por Hipoxia/efectos de los fármacos , Anestésicos por Inhalación/efectos adversos , Supervivencia Celular/efectos de los fármacos , Humanos , Estudios Longitudinales
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