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Dive into the research topics where M. Hernández is active.

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Featured researches published by M. Hernández.


Experimental Eye Research | 2008

Retinal ganglion cell neuroprotection in a rat model of glaucoma following brimonidine, latanoprost or combined treatments

M. Hernández; J. Haritz Urcola; Elena Vecino

The aim of the present study is to evaluate the neuroprotective effect of two antiglaucomatous substances, regardless of their hypotensive effect in the eye. Brimonidine, which does not reduce IOP when administered intraperitoneally, and latanoprost, which has a renowned hypotensive effect topically. We examined rat retinal ganglion cell (RGC) survival and size distribution in experimental glaucoma in response to different glaucomatous agents. IOP was elevated by episcleral vein cauterization (EVC) prior to the application of different treatments: (I) PBS application (control group), (II) intraperitoneal administration of brimonidine (a general hypotensive agent), (III) topical application of latanoprost (an ocular hypotensive agent), and (IV) latanoprost combined with brimonidine. After 12 weeks, RGCs were retrogradely labeled with fluorogold and RGC density was analyzed. EVC caused a significant increase (42%) in IOP in each group before drug treatment. After 12weeks of EVC, RGC survival in control vs. EVC rats was 78.9+/-3.2%. No IOP reduction was observed in brimonidine injected rats, but RGC survival at 12 weeks was total (103.7+/-2.7%). In latanoprost treated rats, IOP dropped by around 22% and 94.7+/-3.7% of the RGC population survived. Finally in the latanoprost+brimonidine combined group, IOP was significantly reduced by 25% and 94.4+/-2.2% of RGCs survived. Surprisingly, whereas EVC led to a 6% increase in RGC soma size, brimonidine treatment was associated with a 9% reduction in the soma size of RGCs at 12 weeks. We conclude that brimonidine exerts a neuroprotective effect via a mechanism which is independent of IOP reduction. These findings indicate that cell survival in glaucoma may be enhanced by neuroprotective strategies which are independent of IOP reduction. No synergistic neuroprotective effect was observed when both treatments were applied simultaneously.


Investigative Ophthalmology & Visual Science | 2010

Altered expression of retinal molecular markers in the canine RPE65 model of Leber congenital amaurosis.

M. Hernández; Susan E. Pearce-Kelling; F. David Rodríguez; Gustavo D. Aguirre; Elena Vecino

PURPOSE Leber congenital amaurosis (LCA) is a group of childhood-onset retinal diseases characterized by severe visual impairment or blindness. One form is caused by mutations in the RPE65 gene, which encodes the retinal pigment epithelium (RPE) isomerase. In this study, the retinal structure and expression of molecular markers for different retinal cell types were characterized, and differences between control and RPE65 mutant dogs during the temporal evolution of the disease were analyzed. METHODS Retinas from normal and mutant dogs of different ages were examined by immunofluorescence with a panel of 16 different antibodies. RESULTS Cones and rods were preserved in the mutant retinas, and the number of cones was normal. However, there was altered expression of cone arrestin and delocalization of rod opsin. The ON bipolar cells showed sprouting of the dendritic arbors toward the outer nuclear layer (ONL) and retraction of their axons in the inner nuclear layer (INL). A decreased expression of GABA, and an increased expression of intermediate filament glial markers was also found in the mutant retinas. These changes were more evident in the adult than the young mutant retinas. CONCLUSIONS The structure of the retina is well preserved in the mutant retina, but several molecular changes take place in photoreceptors and in bipolar and amacrine cells. Some of these changes are structural, whereas others reflect a change in localization of the examined proteins. This study provides new information that can be applied to the interpretation of outcomes of retinal gene therapy in animal models and humans.


Revista De Historia Economica | 1992

La decadencia de la ganadería trashumante en la Sierra de Cameros (1780-1821)

M. Hernández

El trabajo tiene como objetivo fundamental analizar las causas de la crisis y decadencia de la cabana ovina trashumante de ganaderos de la Sierra de Cameros, ejemplificado en el caso de don Mariano Antonio Manso de Velasco, que vendio sus rebanos, como parte de los demas, hacia 1821. El motivo principal fue la subida de los costes de la propia cabana, y muy especialmente la del precio de los pastos en Extremadura, antes de que otros factores como las dificultades en el comercio exterior les pudieran influir. Los factores institucionales, derivados de la toma del poder por los liberales en 1821, tambien desempenarn un importante papel.


Experimental Eye Research | 2005

The pig eye as a novel model of glaucoma

Javier Ruiz-Ederra; Mónica García; M. Hernández; Haritz Urcola; Ernesto Hernández-Barbáchano; Javier Araiz; Elena Vecino


Experimental Eye Research | 2006

Three experimental glaucoma models in rats: Comparison of the effects of intraocular pressure elevation on retinal ganglion cell size and death

J. Haritz Urcola; M. Hernández; Elena Vecino


The International Journal of Developmental Biology | 2004

Cell death in the developing vertebrate retina

Elena Vecino; M. Hernández; Mónica García


Molecular Vision | 2009

Immunohistochemical changes in rat retinas at various time periods of elevated intraocular pressure

M. Hernández; F. David Rodríguez; S.C. Sharma; Elena Vecino


The International Journal of Developmental Biology | 2007

NMDA-receptor blockade enhances cell apoptosis in the developing retina of the postnatal rat

M. Hernández; Inmaculada Guerrikagoitia; Luis Martínez-Millán; Elena Vecino


Investigative Ophthalmology & Visual Science | 2005

Selective Fluorogold and Dextranamine Retrograde Labeling of Retinal Ganglion Cells in Glaucoma

M. Hernández; H. Urcola; Mónica García; J. Ruiz–Ederra; Javier Araiz; Juan A. Durán; Elena Vecino


Investigative Ophthalmology & Visual Science | 2004

Topography Of Retinal Ganglion Cells Of The Pig Retina – Cell Size Distribution

Elena Vecino; J. Ruiz–Ederra; M. Hernández; Ja Urcola; Javier Araiz; Juan A. Durán; Mónica García

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Elena Vecino

University of the Basque Country

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Mónica García

University of the Basque Country

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Javier Araiz

University of the Basque Country

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Juan A. Durán

University of the Basque Country

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J. Ruiz–Ederra

University of the Basque Country

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H. Urcola

University of the Basque Country

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D. Rodriguez

University of Salamanca

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J. Haritz Urcola

University of the Basque Country

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