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1.
Neuroscience ; 380: 152-163, 2018 06 01.
Artículo en Inglés | MEDLINE | ID: mdl-29588252

RESUMEN

While the VGF-derived TLQP peptides have been shown to prevent neuronal apoptosis, and to act on synaptic strengthening, their involvement in Amyotrophic Lateral Sclerosis (ALS) remains unclarified. We studied human ALS patients' plasma (taken at early to late disease stages) and primary fibroblast cultures (patients vs controls), in parallel with SOD1-G93A transgenic mice (taken at pre-, early- and late symptomatic stages) and the mouse motor neuron cell line (NSC-34) treated with Sodium Arsenite (SA) to induce oxidative stress. TLQP peptides were measured by enzyme-linked immunosorbent assay, in parallel with gel chromatography characterization, while their localization was studied by immunohistochemistry. In controls, TLQP peptides, including forms compatible with TLQP-21 and 62, were revealed in plasma and spinal cord motor neurons, as well as in fibroblasts and NSC-34 cells. TLQP peptides were reduced in ALS patients' plasma starting in the early disease stage (14% of controls) and remaining so at the late stage (16% of controls). In mice, a comparable pattern of reduction was shown (vs wild type), in both plasma and spinal cord already in the pre-symptomatic phase (about 26% and 70%, respectively). Similarly, the levels of TLQP peptides were reduced in ALS fibroblasts (31% of controls) and in the NSC-34 treated with Sodium Arsenite (53% of decrease), however, the exogeneous TLQP-21 improved cell viability (SA-treated cells with TLQP-21, vs SA-treated cells only: about 83% vs. 75%). Hence, TLQP peptides, reduced upon oxidative stress, are suggested as blood biomarkers, while TLQP-21 exerts a neuroprotective activity.


Asunto(s)
Esclerosis Amiotrófica Lateral/sangre , Biomarcadores/sangre , Neuroprotección/fisiología , Fragmentos de Péptidos/sangre , Adulto , Anciano , Anciano de 80 o más Años , Animales , Femenino , Humanos , Masculino , Ratones , Ratones Transgénicos , Persona de Mediana Edad , Fármacos Neuroprotectores/farmacología , Fragmentos de Péptidos/farmacología , Péptidos/sangre
2.
PLoS One ; 10(11): e0141193, 2015.
Artículo en Inglés | MEDLINE | ID: mdl-26555143

RESUMEN

VGF mRNA is induced in specific hypothalamic areas of the Siberian hamster upon exposure to short photoperiods, which is associated with a seasonal decrease in appetite and weight loss. Processing of VGF generates multiple bioactive peptides, so the objective of this study was to determine the profile of the VGF-derived peptides in the brain, pituitary and plasma from Siberian hamsters, and to establish whether differential processing might occur in the short day lean state versus long day fat. Antisera against short sequences at the C- or N- termini of proVGF, as well as against NERP-1, TPGH and TLQP peptides, were used for analyses of tissues, and both immunohistochemistry and enzyme linked immunosorbent assay (ELISA) coupled with high-performance liquid (HPLC) or gel chromatography were carried out. VGF peptide immunoreactivity was found within cortex cholinergic perikarya, in multiple hypothalamic nuclei, including those containing vasopressin, and in pituitary gonadotrophs. ELISA revealed that exposure to short day photoperiod led to a down-regulation of VGF immunoreactivity in the cortex, and a less pronounced decrease in the hypothalamus and pituitary, while the plasma VGF levels were not affected by the photoperiod. HPLC and gel chromatography both confirmed the presence of multiple VGF-derived peptides in these tissues, while gel chromatography showed the presence of the VGF precursor in all tissues tested except for the cortex. These observations are consistent with the view that VGF-derived peptides have pleiotropic actions related to changing photoperiod, possibly by regulating cholinergic systems in the cortex, vasopressin hypothalamic pathways, and the reproductive axis.


Asunto(s)
Neuropéptidos/fisiología , Phodopus/fisiología , Fotoperiodo , Procesamiento Proteico-Postraduccional/efectos de la radiación , Animales , Peso Corporal/efectos de la radiación , Corteza Cerebral/metabolismo , Neuronas Colinérgicas/metabolismo , Cromatografía en Gel , Cromatografía Líquida de Alta Presión , Cricetinae , Ensayo de Inmunoadsorción Enzimática , Sistema Hipotálamo-Hipofisario/fisiología , Hipotálamo/metabolismo , Masculino , Tamaño de los Órganos/efectos de la radiación , Fragmentos de Péptidos/metabolismo , Hipófisis/metabolismo , Sistema Hipófiso-Suprarrenal/fisiología , ARN Mensajero/biosíntesis , Testículo/fisiología
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