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1.
Int J Neuropsychopharmacol ; 23(1): 53-65, 2020 03 10.
Artículo en Inglés | MEDLINE | ID: mdl-31563948

RESUMEN

BACKGROUND: Evidence from anatomical, pharmacological, and genetic studies supports a role for the neuropeptide melanin concentrating hormone system in modulating emotional and cognitive functions. Genome-wide association studies revealed a potential association between the melanin concentrating hormone receptor (MCHR1) gene locus and schizophrenia, and the largest genome-wide association study conducted to date shows a credible genome-wide association. METHODS: We analyzed MCHR1 and pro-melanin concentrating hormone RNA-Seq expression in the prefrontal cortex in schizophrenia patients and healthy controls. Disruptions in the melanin concentrating hormone system were modeled in the mouse brain by germline deletion of MCHR1 and by conditional ablation of melanin concentrating hormone expressing neurons using a Cre-inducible diphtheria toxin system. RESULTS: MCHR1 expression is decreased in the prefrontal cortex of schizophrenia samples (false discovery rate (FDR) P < .05, CommonMind and PsychEncode combined datasets, n = 901) while pro-melanin concentrating hormone is below the detection threshold. MCHR1 expression decreased with aging (P = 6.6E-57) in human dorsolateral prefrontal cortex. The deletion of MCHR1 was found to lead to behavioral abnormalities mimicking schizophrenia-like phenotypes: hyperactivity, increased stereotypic and repetitive behavior, social impairment, impaired sensorimotor gating, and disrupted cognitive functions. Conditional ablation of pro-melanin concentrating hormone neurons increased repetitive behavior and produced a deficit in sensorimotor gating. CONCLUSIONS: Our study indicates that early disruption of the melanin concentrating hormone system interferes with neurodevelopmental processes, which may contribute to the pathogenesis of schizophrenia. Further neurobiological research on the developmental timing and circuits that are affected by melanin concentrating hormone may lead to a therapeutic target for early prevention of schizophrenia.


Asunto(s)
Hormonas Hipotalámicas/metabolismo , Melaninas/metabolismo , Trastornos de la Memoria/fisiopatología , Hormonas Hipofisarias/metabolismo , Corteza Prefrontal/metabolismo , Receptores de Somatostatina/deficiencia , Receptores de Somatostatina/metabolismo , Esquizofrenia/metabolismo , Esquizofrenia/fisiopatología , Filtrado Sensorial/fisiología , Adolescente , Adulto , Anciano , Anciano de 80 o más Años , Animales , Conducta Animal/fisiología , Niño , Preescolar , Modelos Animales de Enfermedad , Femenino , Feto , Humanos , Lactante , Masculino , Trastornos de la Memoria/etiología , Ratones , Ratones Noqueados , Persona de Mediana Edad , Esquizofrenia/complicaciones , Adulto Joven
2.
J Anal Methods Chem ; 2016: 3217080, 2016.
Artículo en Inglés | MEDLINE | ID: mdl-27738548

RESUMEN

17α-Ethinyl estradiol (EE2), which is used worldwide in the treatment of some cancers and as a contraceptive, is often found in aquatic systems and is considered a pharmaceutically active compound (PhACs) in the environment. Current methods for the determination of this compound, such as chromatography, are expensive and lengthy and require large amounts of toxic organic solvents. In this work, a voltammetric procedure is developed and validated as a screening tool for detecting EE2 in water samples without prior extraction, clean-up, or derivatization steps. Application of the method we elaborate here to EE2 analysis is unprecedented. EE2 detection was carried out using differential pulse adsorptive cathodic stripping voltammetry (DP AdCSV) with a hanging mercury drop electrode (HMDE) in pH 7.0 Britton-Robinson buffer. The electrochemical process of EE2 reduction was investigated by cyclic voltammetry at different scan rates. Electroreduction of the hormone on a mercury electrode exhibited a peak at -1.16 ± 0.02 V versus Ag/AgCl. The experimental parameters were as follows: -0.7 V accumulation potential, 150 s accumulation time, and 60 mV s-1 scan rate. The limit of detection was 0.49 µg L-1 for a preconcentration time of 150 s. Relative standard deviations were less than 13%. The method was applied to the detection of EE2 in water samples with recoveries ranging from 93.7 to 102.5%.

3.
Anal Bioanal Chem ; 407(20): 6171-9, 2015 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-26025553

RESUMEN

Contaminants of emerging concern (CECs) are chemicals, including pharmaceutical and personal care products, not commonly monitored in the aquatic environment. Pharmaceuticals are nowadays considered as an important environmental contaminant. Chromatography methods which require expensive equipment and complicated sample pretreatment are used for detection of CECs in natural water. Thus, in this study we proposed a simple, fast, and low-cost voltammetric method as a screening tool for the determination of CECs in natural water prior to chromatography. A case study was conducted with alprazolam (benzodiazepine). The method was optimized and validated in-house. The limit of quantification was 0.4 µg L(-1) for a 120 s preconcentration time. The recoveries ranged from 93 to 120 % for accuracy tests. A further proposal aim was to determine for the first time the occurrence of alprazolam in Brazilian river water and to evaluate its potential use as a marker of contamination by wastewater.


Asunto(s)
Alprazolam/análisis , Ansiolíticos/análisis , Técnicas Electroquímicas/métodos , Monitoreo del Ambiente/métodos , Agua Dulce/análisis , Contaminantes Químicos del Agua/análisis , Adsorción , Electrodos , Límite de Detección
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