Rescue of retinal function by BDNF in a mouse model of glaucoma.

Vision loss in glaucoma is caused by progressive dysfunction of retinal ganglion cells (RGCs) and optic nerve atrophy. Here, we investigated the effectiveness of BDNF treatment to preserve vision in a glaucoma experimental model. As an established experimental model, we used the DBA/2J mouse, which...

Full description

Bibliographic Details
Main Authors: Luciano Domenici, Nicola Origlia, Benedetto Falsini, Elisa Cerri, Davide Barloscio, Carlotta Fabiani, Marco Sansò, Luca Giovannini
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2014-01-01
Series:PLoS ONE
Online Access:https://doi.org/10.1371/journal.pone.0115579
id doaj-652d5069a7a341b1bcece4e585df9c79
record_format Article
spelling doaj-652d5069a7a341b1bcece4e585df9c792021-03-03T20:10:53ZengPublic Library of Science (PLoS)PLoS ONE1932-62032014-01-01912e11557910.1371/journal.pone.0115579Rescue of retinal function by BDNF in a mouse model of glaucoma.Luciano DomeniciNicola OrigliaBenedetto FalsiniBenedetto FalsiniElisa CerriDavide BarloscioCarlotta FabianiMarco SansòLuca GiovanniniVision loss in glaucoma is caused by progressive dysfunction of retinal ganglion cells (RGCs) and optic nerve atrophy. Here, we investigated the effectiveness of BDNF treatment to preserve vision in a glaucoma experimental model. As an established experimental model, we used the DBA/2J mouse, which develops chronic intraocular pressure (IOP) elevation that mimics primary open-angle glaucoma (POAG). IOP was measured at different ages in DBA/2J mice. Visual function was monitored using the steady-state Pattern Electroretinogram (P-ERG) and visual cortical evoked potentials (VEP). RGC alterations were assessed using Brn3 immunolabeling, and confocal microscope analysis. Human recombinant BDNF was dissolved in physiological solution (0.9% NaCl); the effects of repeated intravitreal injections and topical eye BDNF applications were independently evaluated in DBA/2J mice with ocular hypertension. BDNF level was measured in retinal homogenate by ELISA and western blot. We found a progressive decline of P-ERG and VEP responses in DBA/2J mice between 4 and 7 months of age, in relationship with the development of ocular hypertension and the reduction of Brn3 immunopositive RGCs. Conversely, repeated intravitreal injections (BDNF concentration = 2 µg/µl, volume = 1 µl, for each injection; 1 injection every four days, three injections over two weeks) and topical eye application of BDNF eye-drops (12 µg/µl, 5 µl eye-drop every 48 h for two weeks) were able to rescue visual responses in 7 month DBA/2J mice. In particular, BDNF topical eye treatment recovered P-ERG and VEP impairment increasing the number of Brn3 immunopositive RGCs. We showed that BDNF effects were independent of IOP reduction. Thus, topical eye treatment with BDNF represents a promisingly safe and feasible strategy to preserve visual function and diminish RGC vulnerability to ocular hypertension.https://doi.org/10.1371/journal.pone.0115579
collection DOAJ
language English
format Article
sources DOAJ
author Luciano Domenici
Nicola Origlia
Benedetto Falsini
Benedetto Falsini
Elisa Cerri
Davide Barloscio
Carlotta Fabiani
Marco Sansò
Luca Giovannini
spellingShingle Luciano Domenici
Nicola Origlia
Benedetto Falsini
Benedetto Falsini
Elisa Cerri
Davide Barloscio
Carlotta Fabiani
Marco Sansò
Luca Giovannini
Rescue of retinal function by BDNF in a mouse model of glaucoma.
PLoS ONE
author_facet Luciano Domenici
Nicola Origlia
Benedetto Falsini
Benedetto Falsini
Elisa Cerri
Davide Barloscio
Carlotta Fabiani
Marco Sansò
Luca Giovannini
author_sort Luciano Domenici
title Rescue of retinal function by BDNF in a mouse model of glaucoma.
title_short Rescue of retinal function by BDNF in a mouse model of glaucoma.
title_full Rescue of retinal function by BDNF in a mouse model of glaucoma.
title_fullStr Rescue of retinal function by BDNF in a mouse model of glaucoma.
title_full_unstemmed Rescue of retinal function by BDNF in a mouse model of glaucoma.
title_sort rescue of retinal function by bdnf in a mouse model of glaucoma.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2014-01-01
description Vision loss in glaucoma is caused by progressive dysfunction of retinal ganglion cells (RGCs) and optic nerve atrophy. Here, we investigated the effectiveness of BDNF treatment to preserve vision in a glaucoma experimental model. As an established experimental model, we used the DBA/2J mouse, which develops chronic intraocular pressure (IOP) elevation that mimics primary open-angle glaucoma (POAG). IOP was measured at different ages in DBA/2J mice. Visual function was monitored using the steady-state Pattern Electroretinogram (P-ERG) and visual cortical evoked potentials (VEP). RGC alterations were assessed using Brn3 immunolabeling, and confocal microscope analysis. Human recombinant BDNF was dissolved in physiological solution (0.9% NaCl); the effects of repeated intravitreal injections and topical eye BDNF applications were independently evaluated in DBA/2J mice with ocular hypertension. BDNF level was measured in retinal homogenate by ELISA and western blot. We found a progressive decline of P-ERG and VEP responses in DBA/2J mice between 4 and 7 months of age, in relationship with the development of ocular hypertension and the reduction of Brn3 immunopositive RGCs. Conversely, repeated intravitreal injections (BDNF concentration = 2 µg/µl, volume = 1 µl, for each injection; 1 injection every four days, three injections over two weeks) and topical eye application of BDNF eye-drops (12 µg/µl, 5 µl eye-drop every 48 h for two weeks) were able to rescue visual responses in 7 month DBA/2J mice. In particular, BDNF topical eye treatment recovered P-ERG and VEP impairment increasing the number of Brn3 immunopositive RGCs. We showed that BDNF effects were independent of IOP reduction. Thus, topical eye treatment with BDNF represents a promisingly safe and feasible strategy to preserve visual function and diminish RGC vulnerability to ocular hypertension.
url https://doi.org/10.1371/journal.pone.0115579
work_keys_str_mv AT lucianodomenici rescueofretinalfunctionbybdnfinamousemodelofglaucoma
AT nicolaoriglia rescueofretinalfunctionbybdnfinamousemodelofglaucoma
AT benedettofalsini rescueofretinalfunctionbybdnfinamousemodelofglaucoma
AT benedettofalsini rescueofretinalfunctionbybdnfinamousemodelofglaucoma
AT elisacerri rescueofretinalfunctionbybdnfinamousemodelofglaucoma
AT davidebarloscio rescueofretinalfunctionbybdnfinamousemodelofglaucoma
AT carlottafabiani rescueofretinalfunctionbybdnfinamousemodelofglaucoma
AT marcosanso rescueofretinalfunctionbybdnfinamousemodelofglaucoma
AT lucagiovannini rescueofretinalfunctionbybdnfinamousemodelofglaucoma
_version_ 1714823599646310400