Changes in the inner and outer retinal layers after acute increase of the intraocular pressure in adult albino Swiss mice
In adult albino mice the effects of increased intraocular pressure on the outer retina and its circuitry was investigated at intervals ranging 3–14 weeks. Ocular hypertension (OHT) was induced by cauterizing the vessels draining the anterior part of the mice eye, as recently reported (Salinas-Navarr...
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creator | Cuenca, Nicolás Pinilla, Isabel Fernández-Sánchez, Laura Salinas-Navarro, Manuel Alarcón-Martínez, Luis Avilés-Trigueros, Marcelino de la Villa, Pedro Miralles de Imperial, Jaime Villegas-Pérez, Maria Paz Vidal-Sanz, Manuel |
description | In adult albino mice the effects of increased intraocular pressure on the outer retina and its circuitry was investigated at intervals ranging 3–14 weeks. Ocular hypertension (OHT) was induced by cauterizing the vessels draining the anterior part of the mice eye, as recently reported (Salinas-Navarro et al., 2009a). Electroretinographic (ERG) responses were recorded simultaneously from both eyes and compared each other prior to and at different survival intervals of 2, 8 or 12 weeks after lasering. Animals were processed at 3, 9 or 14 weeks after lasering, and radial sections were obtained in the cryostat and further processed for immunocytochemistry using antibodies against recoverin, γ-transducin, Protein Kinase C-α (PKC-α), calbindin or synaptophysin. The synaptic ribbons were identified using an antibody against the protein bassoon, which labels photoreceptor ribbons and nuclei were identified using TO-PRO. Laser photocoagulation of the perilimbar and episcleral veins of the left eye resulted in an increase in mean intraocular pressure to approximately over twice its baseline by 24
h that was maintained for approximately five days reaching basal levels by 1 week. ERG recordings from the different groups of mice showed their a-, b-wave and scotopic threshold response (STR) amplitudes, when compared to their contralateral fellow eye, reduced to 62%, 52% and 23% at 12 weeks after lasering.
Three weeks after lasering, immunostaining with recoverin and transducin antibodies could not document any changes in the outer nuclear layer (ONL) but both ON-rod bipolar and horizontal cells had lost their dendritic processes in the outer plexiform layer (OPL). Sprouting of horizontal and bipolar cell processes were observed into the ONL. Fourteen weeks after lasering, protein kinase-C antibodies showed morphologic changes of ON-rod bipolar cells and calbindin staining showed abnormal horizontal cells and a loss of their relationship with their presynaptic input. Moreover, at this time, quantitative studies indicate significant diminutions in the number of photoreceptor synaptic ribbons/100 μm, and in the thickness of the outer nuclear and plexiform layer, when compared to their fellow eyes. Increased intraocular pressure in Swiss mice results in permanent alterations of their full field ERG responses and in changes of the inner and outer retinal circuitries. |
doi_str_mv | 10.1016/j.exer.2010.05.020 |
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h that was maintained for approximately five days reaching basal levels by 1 week. ERG recordings from the different groups of mice showed their a-, b-wave and scotopic threshold response (STR) amplitudes, when compared to their contralateral fellow eye, reduced to 62%, 52% and 23% at 12 weeks after lasering.
Three weeks after lasering, immunostaining with recoverin and transducin antibodies could not document any changes in the outer nuclear layer (ONL) but both ON-rod bipolar and horizontal cells had lost their dendritic processes in the outer plexiform layer (OPL). Sprouting of horizontal and bipolar cell processes were observed into the ONL. Fourteen weeks after lasering, protein kinase-C antibodies showed morphologic changes of ON-rod bipolar cells and calbindin staining showed abnormal horizontal cells and a loss of their relationship with their presynaptic input. Moreover, at this time, quantitative studies indicate significant diminutions in the number of photoreceptor synaptic ribbons/100 μm, and in the thickness of the outer nuclear and plexiform layer, when compared to their fellow eyes. Increased intraocular pressure in Swiss mice results in permanent alterations of their full field ERG responses and in changes of the inner and outer retinal circuitries.</description><identifier>ISSN: 0014-4835</identifier><identifier>EISSN: 1096-0007</identifier><identifier>DOI: 10.1016/j.exer.2010.05.020</identifier><identifier>PMID: 20650699</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>Acute Disease ; adult albino mice ; Animals ; bipolar cells ; Calbindins ; Disease Models, Animal ; Electroretinography ; ERG ; Fluorescent Antibody Technique, Indirect ; immunohistochemistry ; Intraocular Pressure ; Male ; Mice ; Microscopy, Confocal ; ocular hypertension ; Ocular Hypertension - complications ; photoreceptors ; Protein Kinase C-alpha - metabolism ; Recoverin - metabolism ; Retinal Degeneration - etiology ; Retinal Degeneration - metabolism ; Retinal Degeneration - physiopathology ; Retinal Photoreceptor Cell Inner Segment - metabolism ; Retinal Photoreceptor Cell Inner Segment - pathology ; Retinal Photoreceptor Cell Outer Segment - metabolism ; Retinal Photoreceptor Cell Outer Segment - pathology ; S100 Calcium Binding Protein G - metabolism ; Synaptophysin - metabolism ; Transducin - metabolism</subject><ispartof>Experimental eye research, 2010-08, Vol.91 (2), p.273-285</ispartof><rights>2010 Elsevier Ltd</rights><rights>Copyright 2010 Elsevier Ltd. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c421t-28f46e520722c07d99d7abdf9002351fb73eace58a3dc7e9a78d22e3548f58fd3</citedby><cites>FETCH-LOGICAL-c421t-28f46e520722c07d99d7abdf9002351fb73eace58a3dc7e9a78d22e3548f58fd3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.exer.2010.05.020$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3548,27923,27924,45994</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20650699$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Cuenca, Nicolás</creatorcontrib><creatorcontrib>Pinilla, Isabel</creatorcontrib><creatorcontrib>Fernández-Sánchez, Laura</creatorcontrib><creatorcontrib>Salinas-Navarro, Manuel</creatorcontrib><creatorcontrib>Alarcón-Martínez, Luis</creatorcontrib><creatorcontrib>Avilés-Trigueros, Marcelino</creatorcontrib><creatorcontrib>de la Villa, Pedro</creatorcontrib><creatorcontrib>Miralles de Imperial, Jaime</creatorcontrib><creatorcontrib>Villegas-Pérez, Maria Paz</creatorcontrib><creatorcontrib>Vidal-Sanz, Manuel</creatorcontrib><title>Changes in the inner and outer retinal layers after acute increase of the intraocular pressure in adult albino Swiss mice</title><title>Experimental eye research</title><addtitle>Exp Eye Res</addtitle><description>In adult albino mice the effects of increased intraocular pressure on the outer retina and its circuitry was investigated at intervals ranging 3–14 weeks. Ocular hypertension (OHT) was induced by cauterizing the vessels draining the anterior part of the mice eye, as recently reported (Salinas-Navarro et al., 2009a). Electroretinographic (ERG) responses were recorded simultaneously from both eyes and compared each other prior to and at different survival intervals of 2, 8 or 12 weeks after lasering. Animals were processed at 3, 9 or 14 weeks after lasering, and radial sections were obtained in the cryostat and further processed for immunocytochemistry using antibodies against recoverin, γ-transducin, Protein Kinase C-α (PKC-α), calbindin or synaptophysin. The synaptic ribbons were identified using an antibody against the protein bassoon, which labels photoreceptor ribbons and nuclei were identified using TO-PRO. Laser photocoagulation of the perilimbar and episcleral veins of the left eye resulted in an increase in mean intraocular pressure to approximately over twice its baseline by 24
h that was maintained for approximately five days reaching basal levels by 1 week. ERG recordings from the different groups of mice showed their a-, b-wave and scotopic threshold response (STR) amplitudes, when compared to their contralateral fellow eye, reduced to 62%, 52% and 23% at 12 weeks after lasering.
Three weeks after lasering, immunostaining with recoverin and transducin antibodies could not document any changes in the outer nuclear layer (ONL) but both ON-rod bipolar and horizontal cells had lost their dendritic processes in the outer plexiform layer (OPL). Sprouting of horizontal and bipolar cell processes were observed into the ONL. Fourteen weeks after lasering, protein kinase-C antibodies showed morphologic changes of ON-rod bipolar cells and calbindin staining showed abnormal horizontal cells and a loss of their relationship with their presynaptic input. Moreover, at this time, quantitative studies indicate significant diminutions in the number of photoreceptor synaptic ribbons/100 μm, and in the thickness of the outer nuclear and plexiform layer, when compared to their fellow eyes. Increased intraocular pressure in Swiss mice results in permanent alterations of their full field ERG responses and in changes of the inner and outer retinal circuitries.</description><subject>Acute Disease</subject><subject>adult albino mice</subject><subject>Animals</subject><subject>bipolar cells</subject><subject>Calbindins</subject><subject>Disease Models, Animal</subject><subject>Electroretinography</subject><subject>ERG</subject><subject>Fluorescent Antibody Technique, Indirect</subject><subject>immunohistochemistry</subject><subject>Intraocular Pressure</subject><subject>Male</subject><subject>Mice</subject><subject>Microscopy, Confocal</subject><subject>ocular hypertension</subject><subject>Ocular Hypertension - complications</subject><subject>photoreceptors</subject><subject>Protein Kinase C-alpha - metabolism</subject><subject>Recoverin - metabolism</subject><subject>Retinal Degeneration - etiology</subject><subject>Retinal Degeneration - metabolism</subject><subject>Retinal Degeneration - physiopathology</subject><subject>Retinal Photoreceptor Cell Inner Segment - metabolism</subject><subject>Retinal Photoreceptor Cell Inner Segment - pathology</subject><subject>Retinal Photoreceptor Cell Outer Segment - metabolism</subject><subject>Retinal Photoreceptor Cell Outer Segment - pathology</subject><subject>S100 Calcium Binding Protein G - metabolism</subject><subject>Synaptophysin - metabolism</subject><subject>Transducin - metabolism</subject><issn>0014-4835</issn><issn>1096-0007</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kDFv2zAQhYmgReI4-QMZAm6d5JwoUpSALoWRtgECdEgzE2fymNCQJZeU2vjfl4Ldjpnu8O69B9zH2E0JqxLK-m67ojeKKwFZALUCAWdsUUJbFwCgP7AFQCkL2VTqgl2mtM1qJbU8ZxcCagV12y7YYf2K_QslHno-vlIePUWOvePDNOYt0hh67HiHB4qJo59FtPmWrTYSJuKDP0XHiIOdOox8HymlKc4iRzd1I8duE_qBP_0JKfFdsHTFPnrsEl2f5pI9f73_uf5ePP749rD-8lhYKcqxEI2XNSkBWggL2rWt07hxvgUQlSr9RleEllSDlbOaWtSNE4IqJRuvGu-qJft07N3H4ddEaTS7kCx1HfY0TMnoSmZaSkJ2iqPTxiGlSN7sY9hhPJgSzEzcbM1M3MzEDSiTiefQ7al-2uzI_Y_8Q5wNn48Gyk_-DjmebKDekguR7GjcEN7r_wvbnJPB</recordid><startdate>20100801</startdate><enddate>20100801</enddate><creator>Cuenca, Nicolás</creator><creator>Pinilla, Isabel</creator><creator>Fernández-Sánchez, Laura</creator><creator>Salinas-Navarro, Manuel</creator><creator>Alarcón-Martínez, Luis</creator><creator>Avilés-Trigueros, Marcelino</creator><creator>de la Villa, Pedro</creator><creator>Miralles de Imperial, Jaime</creator><creator>Villegas-Pérez, Maria Paz</creator><creator>Vidal-Sanz, Manuel</creator><general>Elsevier Ltd</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>7X8</scope></search><sort><creationdate>20100801</creationdate><title>Changes in the inner and outer retinal layers after acute increase of the intraocular pressure in adult albino Swiss mice</title><author>Cuenca, Nicolás ; Pinilla, Isabel ; Fernández-Sánchez, Laura ; Salinas-Navarro, Manuel ; Alarcón-Martínez, Luis ; Avilés-Trigueros, Marcelino ; de la Villa, Pedro ; Miralles de Imperial, Jaime ; Villegas-Pérez, Maria Paz ; Vidal-Sanz, Manuel</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c421t-28f46e520722c07d99d7abdf9002351fb73eace58a3dc7e9a78d22e3548f58fd3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Acute Disease</topic><topic>adult albino mice</topic><topic>Animals</topic><topic>bipolar cells</topic><topic>Calbindins</topic><topic>Disease Models, Animal</topic><topic>Electroretinography</topic><topic>ERG</topic><topic>Fluorescent Antibody Technique, Indirect</topic><topic>immunohistochemistry</topic><topic>Intraocular Pressure</topic><topic>Male</topic><topic>Mice</topic><topic>Microscopy, Confocal</topic><topic>ocular hypertension</topic><topic>Ocular Hypertension - complications</topic><topic>photoreceptors</topic><topic>Protein Kinase C-alpha - metabolism</topic><topic>Recoverin - metabolism</topic><topic>Retinal Degeneration - etiology</topic><topic>Retinal Degeneration - metabolism</topic><topic>Retinal Degeneration - physiopathology</topic><topic>Retinal Photoreceptor Cell Inner Segment - metabolism</topic><topic>Retinal Photoreceptor Cell Inner Segment - pathology</topic><topic>Retinal Photoreceptor Cell Outer Segment - metabolism</topic><topic>Retinal Photoreceptor Cell Outer Segment - pathology</topic><topic>S100 Calcium Binding Protein G - metabolism</topic><topic>Synaptophysin - metabolism</topic><topic>Transducin - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Cuenca, Nicolás</creatorcontrib><creatorcontrib>Pinilla, Isabel</creatorcontrib><creatorcontrib>Fernández-Sánchez, Laura</creatorcontrib><creatorcontrib>Salinas-Navarro, Manuel</creatorcontrib><creatorcontrib>Alarcón-Martínez, Luis</creatorcontrib><creatorcontrib>Avilés-Trigueros, Marcelino</creatorcontrib><creatorcontrib>de la Villa, Pedro</creatorcontrib><creatorcontrib>Miralles de Imperial, Jaime</creatorcontrib><creatorcontrib>Villegas-Pérez, Maria Paz</creatorcontrib><creatorcontrib>Vidal-Sanz, Manuel</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Experimental eye research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Cuenca, Nicolás</au><au>Pinilla, Isabel</au><au>Fernández-Sánchez, Laura</au><au>Salinas-Navarro, Manuel</au><au>Alarcón-Martínez, Luis</au><au>Avilés-Trigueros, Marcelino</au><au>de la Villa, Pedro</au><au>Miralles de Imperial, Jaime</au><au>Villegas-Pérez, Maria Paz</au><au>Vidal-Sanz, Manuel</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Changes in the inner and outer retinal layers after acute increase of the intraocular pressure in adult albino Swiss mice</atitle><jtitle>Experimental eye research</jtitle><addtitle>Exp Eye Res</addtitle><date>2010-08-01</date><risdate>2010</risdate><volume>91</volume><issue>2</issue><spage>273</spage><epage>285</epage><pages>273-285</pages><issn>0014-4835</issn><eissn>1096-0007</eissn><abstract>In adult albino mice the effects of increased intraocular pressure on the outer retina and its circuitry was investigated at intervals ranging 3–14 weeks. Ocular hypertension (OHT) was induced by cauterizing the vessels draining the anterior part of the mice eye, as recently reported (Salinas-Navarro et al., 2009a). Electroretinographic (ERG) responses were recorded simultaneously from both eyes and compared each other prior to and at different survival intervals of 2, 8 or 12 weeks after lasering. Animals were processed at 3, 9 or 14 weeks after lasering, and radial sections were obtained in the cryostat and further processed for immunocytochemistry using antibodies against recoverin, γ-transducin, Protein Kinase C-α (PKC-α), calbindin or synaptophysin. The synaptic ribbons were identified using an antibody against the protein bassoon, which labels photoreceptor ribbons and nuclei were identified using TO-PRO. Laser photocoagulation of the perilimbar and episcleral veins of the left eye resulted in an increase in mean intraocular pressure to approximately over twice its baseline by 24
h that was maintained for approximately five days reaching basal levels by 1 week. ERG recordings from the different groups of mice showed their a-, b-wave and scotopic threshold response (STR) amplitudes, when compared to their contralateral fellow eye, reduced to 62%, 52% and 23% at 12 weeks after lasering.
Three weeks after lasering, immunostaining with recoverin and transducin antibodies could not document any changes in the outer nuclear layer (ONL) but both ON-rod bipolar and horizontal cells had lost their dendritic processes in the outer plexiform layer (OPL). Sprouting of horizontal and bipolar cell processes were observed into the ONL. Fourteen weeks after lasering, protein kinase-C antibodies showed morphologic changes of ON-rod bipolar cells and calbindin staining showed abnormal horizontal cells and a loss of their relationship with their presynaptic input. Moreover, at this time, quantitative studies indicate significant diminutions in the number of photoreceptor synaptic ribbons/100 μm, and in the thickness of the outer nuclear and plexiform layer, when compared to their fellow eyes. Increased intraocular pressure in Swiss mice results in permanent alterations of their full field ERG responses and in changes of the inner and outer retinal circuitries.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>20650699</pmid><doi>10.1016/j.exer.2010.05.020</doi><tpages>13</tpages></addata></record> |
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subjects | Acute Disease adult albino mice Animals bipolar cells Calbindins Disease Models, Animal Electroretinography ERG Fluorescent Antibody Technique, Indirect immunohistochemistry Intraocular Pressure Male Mice Microscopy, Confocal ocular hypertension Ocular Hypertension - complications photoreceptors Protein Kinase C-alpha - metabolism Recoverin - metabolism Retinal Degeneration - etiology Retinal Degeneration - metabolism Retinal Degeneration - physiopathology Retinal Photoreceptor Cell Inner Segment - metabolism Retinal Photoreceptor Cell Inner Segment - pathology Retinal Photoreceptor Cell Outer Segment - metabolism Retinal Photoreceptor Cell Outer Segment - pathology S100 Calcium Binding Protein G - metabolism Synaptophysin - metabolism Transducin - metabolism |
title | Changes in the inner and outer retinal layers after acute increase of the intraocular pressure in adult albino Swiss mice |
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