Analysis of N1-acetyl-N2-formyl-5-methoxykynuramine/N1-acetyl-5-methoxy-kynuramine formation from melatonin in mice

The interactions of melatonin, a potent endogenous antioxidant, with reactive oxygen species generate several products that include N(1)-acetyl-N(2)-formyl-5-methoxykynuramine (AFMK) and N(1)-acetyl-5-methoxy-kynuramine (AMK). The physiological or pathological significance of AFMK/AMK formation during the process of melatonin metabolism in mammals has not been clarified. Using a metabolomic approach in the current study, the AFMK/AMK pathway was thoroughly investigated both in mice and humans. Unexpectedly, AFMK and AMK were not identified in the urine of humans nor in the urine, feces or tissues (including liver, brain, and eyes) in mice under the current experimental conditions. Metabolomic analysis did identify novel metabolites of AMK, i.e. hydroxy-AMK and glucuronide-conjugated hydroxy-AMK. These two newly identified metabolites were, however, not found in the urine of humans. In addition, oxidative stress induced by acetaminophen in the mouse model did not boost AFMK/AMK formation. These data suggest that AFMK/AMK formation is not a significant pathway of melatonin disposition in mice, even under conditions of oxidative stress.

Urinary metabolites and antioxidant products of exogenous melatonin in the mouse

Exogenous melatonin is widely used for sleep disorders and has potential value in neuroprotection, cardioprotection and as an antioxidant. Here, a novel method is described for the determination of melatonin and six metabolites in mouse urine by use of LC-MS/MS and GC-MS. LC-MS/MS is used for the measurement of melatonin, N1-acetyl-5-methoxykynuramine (AMK), N1-acetyl-N2-formyl-5-methoxykynuramine (AFMK) and 6-hydroxymelatonin (6-HMEL), while GC/MS is used for the determination of N-[2-(5-methoxy-2-oxo-2,3-dihydro-1H-indol-3-yl)-ethyl]-acetamide (2-OMEL) and cyclic 3-hydroxymelatonin (3-HMEL) with detection limits on column of 0.02-0.5 pmol, depending on the metabolite. Following oral administration of melatonin to mice, a 0-24 hr urine collection revealed the presence of melatonin (0.2% dose), 6-HMEL (37.1%) and NAS (3.1%) comprising >90% of the total metabolites; AMK and AFMK were also detected at 0.01% each; 2-OMEL was found at 2.2% of the dose, which is >100 times more than the AMK/AFMK pathway, and comprises >5% of the melatonin-related material detected in mouse urine. 3-HMEL was largely found as a sulfate conjugate. These studies establish sensitive assays for determination of six melatonin metabolites in mouse urine and confirm the potential for antioxidant activity of melatonin through the identification in vivo of AMK and AFMK, ring-opened metabolites with a high capacity for scavenging reactive oxygen species.

A identificación do superdotado a través dos seus estilos de aprendizaxe : resultados dun estudo. 'La identificación del superdotado a través de sus estilos de aprendizaje : resultados de un estudio'.

Contiene anexo con el inventario de variables que intervienen en el aprendizaje

Eficacia dun procedemento de instrución para a substitución de actos comunicativos prelingüísticos. 'Eficacia de un procedimiento de instrucción para sustitución de actos comunicativos prelingüísticos'.

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A tan in a test tube -in vitro models for investigating ultraviolet radiation-induced damage in skin

Presently, global rates of skin cancers induced by ultraviolet radiation (UVR) exposure are on the rise. In view of this, current knowledge gaps in the biology of photocarcinogenesis and skin cancer progression urgently need to be addressed. One factor that has limited skin cancer research has been the need for a reproducible and physiologically-relevant model able to represent the complexity of human skin. This review outlines the main currently-used in vitro models of UVR-induced skin damage. This includes the use of conventional two-dimensional cell culture techniques and the major animal models that have been employed in photobiology and photocarcinogenesis research. Additionally, the progression towards the use of cultured skin explants and tissue-engineered skin constructs, and their utility as models of native skin's responses to UVR are described. The inherent advantages and disadvantages of these in vitro systems are also discussed.

Tan spot: A new disease of pyrethrum caused by Microsphaeropsis tanaceti sp. nov

The isolation frequency of Microsphaeropsis sp. in spring in association with necrotic lesions on leaves in Tasmanian pyrethrum (Tanacetum cinerariifolium) fields has increased substantially since first identification in 2001. Examination of morphological features and sequencing of the internal transcribed spacer region (ITS) resulted in the identification of a new species, herein described as Microsphaeropsis tanaceti sp. nov. The pathogenicity of three M. tanaceti isolates to two pyrethrum cultivars was confirmed by inoculating glasshouse-grown plants in three experiments. No significant differences in the susceptibility of the two cultivars to infection by M. tanaceti were found. Symptoms were tan-coloured spots which coalesced around the margins of the leaves. Therefore, the name 'tan spot' is proposed for this new disease of pyrethrum. The sensitivity of seven M. tanaceti isolates to difenoconazole and azoxystrobin, commonly used fungicides for the management of foliar diseases in spring, was assessed under in vitro conditions. Sensitivity testing for difenoconazole was conducted using a mycelial growth assay on potato dextrose agar, whilst testing for sensitivity to azoxystrobin used a conidial germination assay on water agar. Microsphaeropsis tanaceti was found to be more sensitive to azoxystrobin than difenoconazole, with complete inhibition of conidial germination at concentrations above 0.625 µg a.i. mL-1. By comparison, concentrations of 50 µg a.i. difenoconazole mL-1 or greater were required for significant inhibition of mycelial growth. It therefore appears likely that there is currently some control of tan spot as a result of the use of azoxystrobin and to a lesser extent, difenoconazole, for the control of other diseases.

¿Por qué son tan útiles los metales?

Duración (en horas): De 11 a 20 horas. Nivel educativo: Grado

¿Por qué la materia es tan diversa y tiene propiedades tan distintas?

uración (en horas): De 11 a 20 horas. Nivel educativo: Grado

¿Es tan perjudicial la televisión que ven los jóvenes y adolescentes?

[Es] En este trabajo se presentan los resultados de un estudio piloto realizado en la Comunidad Autónoma del País Vasco con una muestra de sujetos con edades comprendidas entre 12 y 40 años. Dentro de una investigación más amplia donde se pretende relacionar la dieta televisiva y los valores implícitos y explícitos que se perciben en los contenidos televisivos, se exponen algunas diferencias y semejanzas respecto a los hábitos y dieta televisiva de los diferentes grupos de edad. Los datos encontrados nos permiten concluir que los programas más visionados no son los más perniciosos para adolescentes y jóvenes, ni tampoco que el visionado de la televisión impida el desarrollo de otro tipo de actividades.

Encuentros y desencuentros entre el Desarrollo Humano y el Desarrollo Sostenible ¿Qué tan sostenible es el Desarrollo Humano Sostenible?: Los ineludibles límites que se plantean desde la Economía Ecológica

En el presente trabajo se realiza una revisión del concepto de Desarrollo Humano Sostenible (DHS) propuesto por Sudhir Anand y Amartya Sen. En el DHS confluyen el Desarrollo Humano (DH) y el Desarrollo Sostenible (DS), y se presenta como un marco apropiado para abordar la dicotomía entre los procesos de desarrollo y el uso sostenible del medio ambiente. Sin embargo, un análisis conceptual de los planteamientos iniciales del DHS sugiere que tal confluencia no es tan automática dadas las diferentes corrientes del DS en disputa (sostenibilidad débil, fuerte o super-fuerte). En este sentido, las implicaciones conceptuales del DHS, fundamentadas desde la sostenibilidad débil, son contrastadas tomando como referencia los planteamientos de la sostenibilidad fuerte provenientes de la Economía Ecológica.