Developmental light deprivation transiently reduces the expression of vGluT2 and GluN2B in the rat ventral suprachiasmatic nucleus

The suprachiasmatic nucleus (SCN) is the most important circadian clock in mammals. The SCN synchronizes to environmental light via the retinohypothalamic tract (RHT), which is an axon cluster derived from melanopsin‐expressing intrinsic photosensitive retinal ganglion cells. Investigations on the d...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Synapse (New York, N.Y.) N.Y.), 2023-01, Vol.77 (1), p.e22250-n/a
Hauptverfasser: Reyes‐Méndez, Miriam E., Herrera‐Zamora, J. Manuel, Osuna‐Lopez, Fernando, Aguilar‐Martínez, Irving S., Góngora‐Alfaro, José L., Navarro‐Polanco, Ricardo A., Sánchez‐Pastor, Enrique, Moreno‐Galindo, Eloy G., Alamilla, Javier
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page n/a
container_issue 1
container_start_page e22250
container_title Synapse (New York, N.Y.)
container_volume 77
creator Reyes‐Méndez, Miriam E.
Herrera‐Zamora, J. Manuel
Osuna‐Lopez, Fernando
Aguilar‐Martínez, Irving S.
Góngora‐Alfaro, José L.
Navarro‐Polanco, Ricardo A.
Sánchez‐Pastor, Enrique
Moreno‐Galindo, Eloy G.
Alamilla, Javier
description The suprachiasmatic nucleus (SCN) is the most important circadian clock in mammals. The SCN synchronizes to environmental light via the retinohypothalamic tract (RHT), which is an axon cluster derived from melanopsin‐expressing intrinsic photosensitive retinal ganglion cells. Investigations on the development of the nonimage‐forming pathway and the RHT are scarce. Previous studies imply that light stimulation during postnatal development is not needed to make the RHT functional at adult stages. Here, we examined the effects of light deprivation (i.e., constant darkness (DD) rearing) during postnatal development on the expression in the ventral SCN of two crucial proteins for the synchronization of circadian rhythms to light: the presynaptic vesicular glutamate transporter type 2 (vGluT2) and the GluN2B subunit of the postsynaptic NMDA receptor. We found that animals submitted to DD conditions exhibited a transitory reduction in the expression of vGluT2 (at P12–19) and of GluN2B (at P7–9) that was compensated at older stages. These findings support the hypothesis that visual stimulation during early ages is not decisive for normal development of the RHT‐SCN pathway. Graphical The SCN synchronizes to environmental light via the RHT. We analyzed the vGluT2 (RHT) and GluN2B (SCN) immunohistochemical expression during the development of rats reared under LD and DD conditions. DD‐exposed animals exhibited a transitory reduction in the VGluT2 and GluN2B expression that was compensated at older stages. These findings support the hypothesis that visual stimulation during early ages is not decisive for normal development of the RHT‐SCN pathway.
doi_str_mv 10.1002/syn.22250
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2712849505</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2738081015</sourcerecordid><originalsourceid>FETCH-LOGICAL-c2830-768c7435a79801a919902a13aa723966d024f1e34c4d5967e0a1e5a35ea16b6f3</originalsourceid><addsrcrecordid>eNp10c1u1DAUBWALUdGhsOAFkCU2sEh7_ZPEWdICpVJVFpQFq-jWuWFSOU6w44HZ8uR4OoVFpa5syZ-PfH0YeyXgWADIk7j1x1LKEp6wlYDGFFI11VO2AmPqQuu6OmTPY7wFACVAP2OHqgJTaqVW7M8H2pCb5pH8go674cd64R3NYdjgMkyeLwF9HPKp2_JAXbIU-bImTr_nQDHuyNTzzblL15Kj73jeXclTPvg7FnDhm3w75PCY5oB2PWAcc7blPllHKb5gBz26SC_v1yP27dPH67PPxeWX84uz95eFlUZBUVfG1lqVWDcGBDaiaUCiUIj1btyqA6l7QUpb3ZVNVROgoBJVSSiqm6pXR-ztPncO089EcWnHIVpyDj1NKbayFtLopoQy0zcP6O2Ugs-vy0oZMALETr3bKxumGAP1bf62EcO2FdDuimlzMe1dMdm-vk9MNyN1_-W_JjI42YNfg6Pt40nt1-9X-8i_iYuYEQ</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2738081015</pqid></control><display><type>article</type><title>Developmental light deprivation transiently reduces the expression of vGluT2 and GluN2B in the rat ventral suprachiasmatic nucleus</title><source>MEDLINE</source><source>Wiley Online Library Journals Frontfile Complete</source><creator>Reyes‐Méndez, Miriam E. ; Herrera‐Zamora, J. Manuel ; Osuna‐Lopez, Fernando ; Aguilar‐Martínez, Irving S. ; Góngora‐Alfaro, José L. ; Navarro‐Polanco, Ricardo A. ; Sánchez‐Pastor, Enrique ; Moreno‐Galindo, Eloy G. ; Alamilla, Javier</creator><creatorcontrib>Reyes‐Méndez, Miriam E. ; Herrera‐Zamora, J. Manuel ; Osuna‐Lopez, Fernando ; Aguilar‐Martínez, Irving S. ; Góngora‐Alfaro, José L. ; Navarro‐Polanco, Ricardo A. ; Sánchez‐Pastor, Enrique ; Moreno‐Galindo, Eloy G. ; Alamilla, Javier</creatorcontrib><description>The suprachiasmatic nucleus (SCN) is the most important circadian clock in mammals. The SCN synchronizes to environmental light via the retinohypothalamic tract (RHT), which is an axon cluster derived from melanopsin‐expressing intrinsic photosensitive retinal ganglion cells. Investigations on the development of the nonimage‐forming pathway and the RHT are scarce. Previous studies imply that light stimulation during postnatal development is not needed to make the RHT functional at adult stages. Here, we examined the effects of light deprivation (i.e., constant darkness (DD) rearing) during postnatal development on the expression in the ventral SCN of two crucial proteins for the synchronization of circadian rhythms to light: the presynaptic vesicular glutamate transporter type 2 (vGluT2) and the GluN2B subunit of the postsynaptic NMDA receptor. We found that animals submitted to DD conditions exhibited a transitory reduction in the expression of vGluT2 (at P12–19) and of GluN2B (at P7–9) that was compensated at older stages. These findings support the hypothesis that visual stimulation during early ages is not decisive for normal development of the RHT‐SCN pathway. Graphical The SCN synchronizes to environmental light via the RHT. We analyzed the vGluT2 (RHT) and GluN2B (SCN) immunohistochemical expression during the development of rats reared under LD and DD conditions. DD‐exposed animals exhibited a transitory reduction in the VGluT2 and GluN2B expression that was compensated at older stages. These findings support the hypothesis that visual stimulation during early ages is not decisive for normal development of the RHT‐SCN pathway.</description><identifier>ISSN: 0887-4476</identifier><identifier>EISSN: 1098-2396</identifier><identifier>DOI: 10.1002/syn.22250</identifier><identifier>PMID: 36085433</identifier><language>eng</language><publisher>United States: Wiley Subscription Services, Inc</publisher><subject>Animals ; circadian clock ; Circadian rhythm ; Circadian Rhythm - physiology ; Circadian rhythms ; constant darkness ; development ; glutamate ; Glutamic acid receptors (ionotropic) ; Glutamic acid transporter ; Light effects ; Mammals - metabolism ; Melanopsin ; N-Methyl-D-aspartic acid receptors ; nonimage‐forming system ; Rats ; Receptors, N-Methyl-D-Aspartate - genetics ; Receptors, N-Methyl-D-Aspartate - metabolism ; Retinal ganglion cells ; Retinal Ganglion Cells - metabolism ; Suprachiasmatic nucleus ; Suprachiasmatic Nucleus - metabolism ; Synchronization ; Vesicular Glutamate Transport Protein 2 - metabolism ; Visual stimuli</subject><ispartof>Synapse (New York, N.Y.), 2023-01, Vol.77 (1), p.e22250-n/a</ispartof><rights>2022 Wiley Periodicals LLC.</rights><rights>2023 Wiley Periodicals LLC.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c2830-768c7435a79801a919902a13aa723966d024f1e34c4d5967e0a1e5a35ea16b6f3</citedby><cites>FETCH-LOGICAL-c2830-768c7435a79801a919902a13aa723966d024f1e34c4d5967e0a1e5a35ea16b6f3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fsyn.22250$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fsyn.22250$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/36085433$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Reyes‐Méndez, Miriam E.</creatorcontrib><creatorcontrib>Herrera‐Zamora, J. Manuel</creatorcontrib><creatorcontrib>Osuna‐Lopez, Fernando</creatorcontrib><creatorcontrib>Aguilar‐Martínez, Irving S.</creatorcontrib><creatorcontrib>Góngora‐Alfaro, José L.</creatorcontrib><creatorcontrib>Navarro‐Polanco, Ricardo A.</creatorcontrib><creatorcontrib>Sánchez‐Pastor, Enrique</creatorcontrib><creatorcontrib>Moreno‐Galindo, Eloy G.</creatorcontrib><creatorcontrib>Alamilla, Javier</creatorcontrib><title>Developmental light deprivation transiently reduces the expression of vGluT2 and GluN2B in the rat ventral suprachiasmatic nucleus</title><title>Synapse (New York, N.Y.)</title><addtitle>Synapse</addtitle><description>The suprachiasmatic nucleus (SCN) is the most important circadian clock in mammals. The SCN synchronizes to environmental light via the retinohypothalamic tract (RHT), which is an axon cluster derived from melanopsin‐expressing intrinsic photosensitive retinal ganglion cells. Investigations on the development of the nonimage‐forming pathway and the RHT are scarce. Previous studies imply that light stimulation during postnatal development is not needed to make the RHT functional at adult stages. Here, we examined the effects of light deprivation (i.e., constant darkness (DD) rearing) during postnatal development on the expression in the ventral SCN of two crucial proteins for the synchronization of circadian rhythms to light: the presynaptic vesicular glutamate transporter type 2 (vGluT2) and the GluN2B subunit of the postsynaptic NMDA receptor. We found that animals submitted to DD conditions exhibited a transitory reduction in the expression of vGluT2 (at P12–19) and of GluN2B (at P7–9) that was compensated at older stages. These findings support the hypothesis that visual stimulation during early ages is not decisive for normal development of the RHT‐SCN pathway. Graphical The SCN synchronizes to environmental light via the RHT. We analyzed the vGluT2 (RHT) and GluN2B (SCN) immunohistochemical expression during the development of rats reared under LD and DD conditions. DD‐exposed animals exhibited a transitory reduction in the VGluT2 and GluN2B expression that was compensated at older stages. These findings support the hypothesis that visual stimulation during early ages is not decisive for normal development of the RHT‐SCN pathway.</description><subject>Animals</subject><subject>circadian clock</subject><subject>Circadian rhythm</subject><subject>Circadian Rhythm - physiology</subject><subject>Circadian rhythms</subject><subject>constant darkness</subject><subject>development</subject><subject>glutamate</subject><subject>Glutamic acid receptors (ionotropic)</subject><subject>Glutamic acid transporter</subject><subject>Light effects</subject><subject>Mammals - metabolism</subject><subject>Melanopsin</subject><subject>N-Methyl-D-aspartic acid receptors</subject><subject>nonimage‐forming system</subject><subject>Rats</subject><subject>Receptors, N-Methyl-D-Aspartate - genetics</subject><subject>Receptors, N-Methyl-D-Aspartate - metabolism</subject><subject>Retinal ganglion cells</subject><subject>Retinal Ganglion Cells - metabolism</subject><subject>Suprachiasmatic nucleus</subject><subject>Suprachiasmatic Nucleus - metabolism</subject><subject>Synchronization</subject><subject>Vesicular Glutamate Transport Protein 2 - metabolism</subject><subject>Visual stimuli</subject><issn>0887-4476</issn><issn>1098-2396</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp10c1u1DAUBWALUdGhsOAFkCU2sEh7_ZPEWdICpVJVFpQFq-jWuWFSOU6w44HZ8uR4OoVFpa5syZ-PfH0YeyXgWADIk7j1x1LKEp6wlYDGFFI11VO2AmPqQuu6OmTPY7wFACVAP2OHqgJTaqVW7M8H2pCb5pH8go674cd64R3NYdjgMkyeLwF9HPKp2_JAXbIU-bImTr_nQDHuyNTzzblL15Kj73jeXclTPvg7FnDhm3w75PCY5oB2PWAcc7blPllHKb5gBz26SC_v1yP27dPH67PPxeWX84uz95eFlUZBUVfG1lqVWDcGBDaiaUCiUIj1btyqA6l7QUpb3ZVNVROgoBJVSSiqm6pXR-ztPncO089EcWnHIVpyDj1NKbayFtLopoQy0zcP6O2Ugs-vy0oZMALETr3bKxumGAP1bf62EcO2FdDuimlzMe1dMdm-vk9MNyN1_-W_JjI42YNfg6Pt40nt1-9X-8i_iYuYEQ</recordid><startdate>202301</startdate><enddate>202301</enddate><creator>Reyes‐Méndez, Miriam E.</creator><creator>Herrera‐Zamora, J. Manuel</creator><creator>Osuna‐Lopez, Fernando</creator><creator>Aguilar‐Martínez, Irving S.</creator><creator>Góngora‐Alfaro, José L.</creator><creator>Navarro‐Polanco, Ricardo A.</creator><creator>Sánchez‐Pastor, Enrique</creator><creator>Moreno‐Galindo, Eloy G.</creator><creator>Alamilla, Javier</creator><general>Wiley Subscription Services, Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QP</scope><scope>7TK</scope><scope>K9.</scope><scope>7X8</scope></search><sort><creationdate>202301</creationdate><title>Developmental light deprivation transiently reduces the expression of vGluT2 and GluN2B in the rat ventral suprachiasmatic nucleus</title><author>Reyes‐Méndez, Miriam E. ; Herrera‐Zamora, J. Manuel ; Osuna‐Lopez, Fernando ; Aguilar‐Martínez, Irving S. ; Góngora‐Alfaro, José L. ; Navarro‐Polanco, Ricardo A. ; Sánchez‐Pastor, Enrique ; Moreno‐Galindo, Eloy G. ; Alamilla, Javier</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c2830-768c7435a79801a919902a13aa723966d024f1e34c4d5967e0a1e5a35ea16b6f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Animals</topic><topic>circadian clock</topic><topic>Circadian rhythm</topic><topic>Circadian Rhythm - physiology</topic><topic>Circadian rhythms</topic><topic>constant darkness</topic><topic>development</topic><topic>glutamate</topic><topic>Glutamic acid receptors (ionotropic)</topic><topic>Glutamic acid transporter</topic><topic>Light effects</topic><topic>Mammals - metabolism</topic><topic>Melanopsin</topic><topic>N-Methyl-D-aspartic acid receptors</topic><topic>nonimage‐forming system</topic><topic>Rats</topic><topic>Receptors, N-Methyl-D-Aspartate - genetics</topic><topic>Receptors, N-Methyl-D-Aspartate - metabolism</topic><topic>Retinal ganglion cells</topic><topic>Retinal Ganglion Cells - metabolism</topic><topic>Suprachiasmatic nucleus</topic><topic>Suprachiasmatic Nucleus - metabolism</topic><topic>Synchronization</topic><topic>Vesicular Glutamate Transport Protein 2 - metabolism</topic><topic>Visual stimuli</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Reyes‐Méndez, Miriam E.</creatorcontrib><creatorcontrib>Herrera‐Zamora, J. Manuel</creatorcontrib><creatorcontrib>Osuna‐Lopez, Fernando</creatorcontrib><creatorcontrib>Aguilar‐Martínez, Irving S.</creatorcontrib><creatorcontrib>Góngora‐Alfaro, José L.</creatorcontrib><creatorcontrib>Navarro‐Polanco, Ricardo A.</creatorcontrib><creatorcontrib>Sánchez‐Pastor, Enrique</creatorcontrib><creatorcontrib>Moreno‐Galindo, Eloy G.</creatorcontrib><creatorcontrib>Alamilla, Javier</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Calcium &amp; Calcified Tissue Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><jtitle>Synapse (New York, N.Y.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Reyes‐Méndez, Miriam E.</au><au>Herrera‐Zamora, J. Manuel</au><au>Osuna‐Lopez, Fernando</au><au>Aguilar‐Martínez, Irving S.</au><au>Góngora‐Alfaro, José L.</au><au>Navarro‐Polanco, Ricardo A.</au><au>Sánchez‐Pastor, Enrique</au><au>Moreno‐Galindo, Eloy G.</au><au>Alamilla, Javier</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Developmental light deprivation transiently reduces the expression of vGluT2 and GluN2B in the rat ventral suprachiasmatic nucleus</atitle><jtitle>Synapse (New York, N.Y.)</jtitle><addtitle>Synapse</addtitle><date>2023-01</date><risdate>2023</risdate><volume>77</volume><issue>1</issue><spage>e22250</spage><epage>n/a</epage><pages>e22250-n/a</pages><issn>0887-4476</issn><eissn>1098-2396</eissn><abstract>The suprachiasmatic nucleus (SCN) is the most important circadian clock in mammals. The SCN synchronizes to environmental light via the retinohypothalamic tract (RHT), which is an axon cluster derived from melanopsin‐expressing intrinsic photosensitive retinal ganglion cells. Investigations on the development of the nonimage‐forming pathway and the RHT are scarce. Previous studies imply that light stimulation during postnatal development is not needed to make the RHT functional at adult stages. Here, we examined the effects of light deprivation (i.e., constant darkness (DD) rearing) during postnatal development on the expression in the ventral SCN of two crucial proteins for the synchronization of circadian rhythms to light: the presynaptic vesicular glutamate transporter type 2 (vGluT2) and the GluN2B subunit of the postsynaptic NMDA receptor. We found that animals submitted to DD conditions exhibited a transitory reduction in the expression of vGluT2 (at P12–19) and of GluN2B (at P7–9) that was compensated at older stages. These findings support the hypothesis that visual stimulation during early ages is not decisive for normal development of the RHT‐SCN pathway. Graphical The SCN synchronizes to environmental light via the RHT. We analyzed the vGluT2 (RHT) and GluN2B (SCN) immunohistochemical expression during the development of rats reared under LD and DD conditions. DD‐exposed animals exhibited a transitory reduction in the VGluT2 and GluN2B expression that was compensated at older stages. These findings support the hypothesis that visual stimulation during early ages is not decisive for normal development of the RHT‐SCN pathway.</abstract><cop>United States</cop><pub>Wiley Subscription Services, Inc</pub><pmid>36085433</pmid><doi>10.1002/syn.22250</doi><tpages>8</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0887-4476
ispartof Synapse (New York, N.Y.), 2023-01, Vol.77 (1), p.e22250-n/a
issn 0887-4476
1098-2396
language eng
recordid cdi_proquest_miscellaneous_2712849505
source MEDLINE; Wiley Online Library Journals Frontfile Complete
subjects Animals
circadian clock
Circadian rhythm
Circadian Rhythm - physiology
Circadian rhythms
constant darkness
development
glutamate
Glutamic acid receptors (ionotropic)
Glutamic acid transporter
Light effects
Mammals - metabolism
Melanopsin
N-Methyl-D-aspartic acid receptors
nonimage‐forming system
Rats
Receptors, N-Methyl-D-Aspartate - genetics
Receptors, N-Methyl-D-Aspartate - metabolism
Retinal ganglion cells
Retinal Ganglion Cells - metabolism
Suprachiasmatic nucleus
Suprachiasmatic Nucleus - metabolism
Synchronization
Vesicular Glutamate Transport Protein 2 - metabolism
Visual stimuli
title Developmental light deprivation transiently reduces the expression of vGluT2 and GluN2B in the rat ventral suprachiasmatic nucleus
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-11T14%3A47%3A04IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Developmental%20light%20deprivation%20transiently%20reduces%20the%20expression%20of%20vGluT2%20and%20GluN2B%20in%20the%20rat%20ventral%20suprachiasmatic%20nucleus&rft.jtitle=Synapse%20(New%20York,%20N.Y.)&rft.au=Reyes%E2%80%90M%C3%A9ndez,%20Miriam%20E.&rft.date=2023-01&rft.volume=77&rft.issue=1&rft.spage=e22250&rft.epage=n/a&rft.pages=e22250-n/a&rft.issn=0887-4476&rft.eissn=1098-2396&rft_id=info:doi/10.1002/syn.22250&rft_dat=%3Cproquest_cross%3E2738081015%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2738081015&rft_id=info:pmid/36085433&rfr_iscdi=true