Cargando…

Daily visual stimulation in the critical period enhances multiple aspects of vision through BDNF-mediated pathways in the mouse retina

Visual experience during the critical period modulates visual development such that deprivation causes visual impairments while stimulation induces enhancements. This study aimed to determine whether visual stimulation in the form of daily optomotor response (OMR) testing during the mouse critical p...

Descripción completa

Detalles Bibliográficos
Autores principales: Mui, Amanda M., Yang, Victoria, Aung, Moe H., Fu, Jieming, Adekunle, Adewumi N., Prall, Brian C., Sidhu, Curran S., Park, Han na, Boatright, Jeffrey H., Iuvone, P. Michael, Pardue, Machelle T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5800661/
https://www.ncbi.nlm.nih.gov/pubmed/29408880
http://dx.doi.org/10.1371/journal.pone.0192435
_version_ 1783298242856878080
author Mui, Amanda M.
Yang, Victoria
Aung, Moe H.
Fu, Jieming
Adekunle, Adewumi N.
Prall, Brian C.
Sidhu, Curran S.
Park, Han na
Boatright, Jeffrey H.
Iuvone, P. Michael
Pardue, Machelle T.
author_facet Mui, Amanda M.
Yang, Victoria
Aung, Moe H.
Fu, Jieming
Adekunle, Adewumi N.
Prall, Brian C.
Sidhu, Curran S.
Park, Han na
Boatright, Jeffrey H.
Iuvone, P. Michael
Pardue, Machelle T.
author_sort Mui, Amanda M.
collection PubMed
description Visual experience during the critical period modulates visual development such that deprivation causes visual impairments while stimulation induces enhancements. This study aimed to determine whether visual stimulation in the form of daily optomotor response (OMR) testing during the mouse critical period (1) improves aspects of visual function, (2) involves retinal mechanisms and (3) is mediated by brain derived neurotrophic factor (BDNF) and dopamine (DA) signaling pathways. We tested spatial frequency thresholds in C57BL/6J mice daily from postnatal days 16 to 23 (P16 to P23) using OMR testing. Daily OMR-treated mice were compared to littermate controls that were placed in the OMR chamber without moving gratings. Contrast sensitivity thresholds, electroretinograms (ERGs), visual evoked potentials, and pattern ERGs were acquired at P21. To determine the role of BDNF signaling, a TrkB receptor antagonist (ANA-12) was systemically injected 2 hours prior to OMR testing in another cohort of mice. BDNF immunohistochemistry was performed on retina and brain sections. Retinal DA levels were measured using high-performance liquid chromatography. Daily OMR testing enhanced spatial frequency thresholds and contrast sensitivity compared to controls. OMR-treated mice also had improved rod-driven ERG oscillatory potential response times, greater BDNF immunoreactivity in the retinal ganglion cell layer, and increased retinal DA content compared to controls. VEPs and pattern ERGs were unchanged. Systemic delivery of ANA-12 attenuated OMR-induced visual enhancements. Daily OMR testing during the critical period leads to general visual function improvements accompanied by increased DA and BDNF in the retina, with this process being requisitely mediated by TrkB activation. These results suggest that novel combination therapies involving visual stimulation and using both behavioral and molecular approaches may benefit degenerative retinal diseases or amblyopia.
format Online
Article
Text
id pubmed-5800661
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-58006612018-02-23 Daily visual stimulation in the critical period enhances multiple aspects of vision through BDNF-mediated pathways in the mouse retina Mui, Amanda M. Yang, Victoria Aung, Moe H. Fu, Jieming Adekunle, Adewumi N. Prall, Brian C. Sidhu, Curran S. Park, Han na Boatright, Jeffrey H. Iuvone, P. Michael Pardue, Machelle T. PLoS One Research Article Visual experience during the critical period modulates visual development such that deprivation causes visual impairments while stimulation induces enhancements. This study aimed to determine whether visual stimulation in the form of daily optomotor response (OMR) testing during the mouse critical period (1) improves aspects of visual function, (2) involves retinal mechanisms and (3) is mediated by brain derived neurotrophic factor (BDNF) and dopamine (DA) signaling pathways. We tested spatial frequency thresholds in C57BL/6J mice daily from postnatal days 16 to 23 (P16 to P23) using OMR testing. Daily OMR-treated mice were compared to littermate controls that were placed in the OMR chamber without moving gratings. Contrast sensitivity thresholds, electroretinograms (ERGs), visual evoked potentials, and pattern ERGs were acquired at P21. To determine the role of BDNF signaling, a TrkB receptor antagonist (ANA-12) was systemically injected 2 hours prior to OMR testing in another cohort of mice. BDNF immunohistochemistry was performed on retina and brain sections. Retinal DA levels were measured using high-performance liquid chromatography. Daily OMR testing enhanced spatial frequency thresholds and contrast sensitivity compared to controls. OMR-treated mice also had improved rod-driven ERG oscillatory potential response times, greater BDNF immunoreactivity in the retinal ganglion cell layer, and increased retinal DA content compared to controls. VEPs and pattern ERGs were unchanged. Systemic delivery of ANA-12 attenuated OMR-induced visual enhancements. Daily OMR testing during the critical period leads to general visual function improvements accompanied by increased DA and BDNF in the retina, with this process being requisitely mediated by TrkB activation. These results suggest that novel combination therapies involving visual stimulation and using both behavioral and molecular approaches may benefit degenerative retinal diseases or amblyopia. Public Library of Science 2018-02-06 /pmc/articles/PMC5800661/ /pubmed/29408880 http://dx.doi.org/10.1371/journal.pone.0192435 Text en https://creativecommons.org/publicdomain/zero/1.0/ This is an open access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 (https://creativecommons.org/publicdomain/zero/1.0/) public domain dedication.
spellingShingle Research Article
Mui, Amanda M.
Yang, Victoria
Aung, Moe H.
Fu, Jieming
Adekunle, Adewumi N.
Prall, Brian C.
Sidhu, Curran S.
Park, Han na
Boatright, Jeffrey H.
Iuvone, P. Michael
Pardue, Machelle T.
Daily visual stimulation in the critical period enhances multiple aspects of vision through BDNF-mediated pathways in the mouse retina
title Daily visual stimulation in the critical period enhances multiple aspects of vision through BDNF-mediated pathways in the mouse retina
title_full Daily visual stimulation in the critical period enhances multiple aspects of vision through BDNF-mediated pathways in the mouse retina
title_fullStr Daily visual stimulation in the critical period enhances multiple aspects of vision through BDNF-mediated pathways in the mouse retina
title_full_unstemmed Daily visual stimulation in the critical period enhances multiple aspects of vision through BDNF-mediated pathways in the mouse retina
title_short Daily visual stimulation in the critical period enhances multiple aspects of vision through BDNF-mediated pathways in the mouse retina
title_sort daily visual stimulation in the critical period enhances multiple aspects of vision through bdnf-mediated pathways in the mouse retina
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5800661/
https://www.ncbi.nlm.nih.gov/pubmed/29408880
http://dx.doi.org/10.1371/journal.pone.0192435
work_keys_str_mv AT muiamandam dailyvisualstimulationinthecriticalperiodenhancesmultipleaspectsofvisionthroughbdnfmediatedpathwaysinthemouseretina
AT yangvictoria dailyvisualstimulationinthecriticalperiodenhancesmultipleaspectsofvisionthroughbdnfmediatedpathwaysinthemouseretina
AT aungmoeh dailyvisualstimulationinthecriticalperiodenhancesmultipleaspectsofvisionthroughbdnfmediatedpathwaysinthemouseretina
AT fujieming dailyvisualstimulationinthecriticalperiodenhancesmultipleaspectsofvisionthroughbdnfmediatedpathwaysinthemouseretina
AT adekunleadewumin dailyvisualstimulationinthecriticalperiodenhancesmultipleaspectsofvisionthroughbdnfmediatedpathwaysinthemouseretina
AT prallbrianc dailyvisualstimulationinthecriticalperiodenhancesmultipleaspectsofvisionthroughbdnfmediatedpathwaysinthemouseretina
AT sidhucurrans dailyvisualstimulationinthecriticalperiodenhancesmultipleaspectsofvisionthroughbdnfmediatedpathwaysinthemouseretina
AT parkhanna dailyvisualstimulationinthecriticalperiodenhancesmultipleaspectsofvisionthroughbdnfmediatedpathwaysinthemouseretina
AT boatrightjeffreyh dailyvisualstimulationinthecriticalperiodenhancesmultipleaspectsofvisionthroughbdnfmediatedpathwaysinthemouseretina
AT iuvonepmichael dailyvisualstimulationinthecriticalperiodenhancesmultipleaspectsofvisionthroughbdnfmediatedpathwaysinthemouseretina
AT parduemachellet dailyvisualstimulationinthecriticalperiodenhancesmultipleaspectsofvisionthroughbdnfmediatedpathwaysinthemouseretina