Trabodenoson, an Adenosine Mimetic With A1 Receptor Selectivity Lowers Intraocular Pressure by Increasing Conventional Outflow Facility in Mice
To evaluate the relationship between the IOP-lowering effect of trabodenoson and the associated structural and functional changes in the trabecular meshwork (TM). Six independent cohorts of young and aged mice were exposed to three different topical once-a-day formulations of trabodenoson and eyes w...
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Veröffentlicht in: | Investigative ophthalmology & visual science 2018-01, Vol.59 (1), p.383-392 |
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creator | Li, Guorong Torrejon, Karen Y Unser, Andrea M Ahmed, Feryan Navarro, Iris D Baumgartner, Rudolf A Albers, David S Stamer, W Daniel |
description | To evaluate the relationship between the IOP-lowering effect of trabodenoson and the associated structural and functional changes in the trabecular meshwork (TM).
Six independent cohorts of young and aged mice were exposed to three different topical once-a-day formulations of trabodenoson and eyes were compared to those treated with placebo drops. IOP was measured daily just before drug administration using rebound tonometry. Outflow facility was measured in enucleated eyes. Flow patterns and morphology of conventional outflow tissues were monitored using tracer beads and standard histology, respectively. In parallel, three-dimensional human TM tissue constructs (3D-HTM) were grown and used in experiments to test effect of trabodenoson on the expression of collagen IV, fibronectin, matrix metalloproteinase (MMP)-2 and MMP-14 plus MMP-2 activity.
Topical administration of trabodenoson significantly lowered IOP on every day tested, up to 7 days. After 2 days of treatment, outflow facility increased by 26% in aged mice and 30% overall (young and aged mice), which was significantly different from vehicle (P < 0.05). Outflow facility was 15% higher than controls after 7 days of treatment (P = 0.07). While gross morphology was not affected by treatment, the intensity of tracer bead distribution increased by day 7 (P = 0.05). Parallel experiments in 3D-HTM showed that trabodenoson treatment significantly increased MMP-2 activity and MMP-14 abundance, while decreasing fibronectin and collagen IV expression.
Trabodenoson alters ECM turnover by TM cells and increases conventional outflow facility, which accounts for its ability to lower IOP in young and aged mice. |
doi_str_mv | 10.1167/iovs.17-23212 |
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Six independent cohorts of young and aged mice were exposed to three different topical once-a-day formulations of trabodenoson and eyes were compared to those treated with placebo drops. IOP was measured daily just before drug administration using rebound tonometry. Outflow facility was measured in enucleated eyes. Flow patterns and morphology of conventional outflow tissues were monitored using tracer beads and standard histology, respectively. In parallel, three-dimensional human TM tissue constructs (3D-HTM) were grown and used in experiments to test effect of trabodenoson on the expression of collagen IV, fibronectin, matrix metalloproteinase (MMP)-2 and MMP-14 plus MMP-2 activity.
Topical administration of trabodenoson significantly lowered IOP on every day tested, up to 7 days. After 2 days of treatment, outflow facility increased by 26% in aged mice and 30% overall (young and aged mice), which was significantly different from vehicle (P < 0.05). Outflow facility was 15% higher than controls after 7 days of treatment (P = 0.07). While gross morphology was not affected by treatment, the intensity of tracer bead distribution increased by day 7 (P = 0.05). Parallel experiments in 3D-HTM showed that trabodenoson treatment significantly increased MMP-2 activity and MMP-14 abundance, while decreasing fibronectin and collagen IV expression.
Trabodenoson alters ECM turnover by TM cells and increases conventional outflow facility, which accounts for its ability to lower IOP in young and aged mice.</description><identifier>ISSN: 0146-0404</identifier><identifier>EISSN: 1552-5783</identifier><identifier>DOI: 10.1167/iovs.17-23212</identifier><identifier>PMID: 29346804</identifier><language>eng</language><publisher>United States: The Association for Research in Vision and Ophthalmology</publisher><subject>Adenosine - pharmacology ; Administration, Ophthalmic ; Animals ; Antihypertensive Agents - pharmacology ; Aqueous Humor - secretion ; Biomimetics ; Blotting, Western ; Cell Line ; Collagen Type IV - metabolism ; Fibronectins - metabolism ; Humans ; Immunohistochemistry ; Intraocular Pressure - drug effects ; Luminescent Measurements ; Matrix Metalloproteinase 14 - metabolism ; Matrix Metalloproteinase 2 - metabolism ; Mice ; Mice, Inbred C57BL ; Microscopy, Confocal ; Nitrates - pharmacology ; Physiology and Pharmacology ; Purines - pharmacology ; Receptor, Adenosine A1 - metabolism ; Tissue Scaffolds ; Tonometry, Ocular ; Trabecular Meshwork - drug effects ; Trabecular Meshwork - metabolism</subject><ispartof>Investigative ophthalmology & visual science, 2018-01, Vol.59 (1), p.383-392</ispartof><rights>Copyright 2018 The Authors 2018</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5774255/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5774255/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,860,881,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29346804$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Li, Guorong</creatorcontrib><creatorcontrib>Torrejon, Karen Y</creatorcontrib><creatorcontrib>Unser, Andrea M</creatorcontrib><creatorcontrib>Ahmed, Feryan</creatorcontrib><creatorcontrib>Navarro, Iris D</creatorcontrib><creatorcontrib>Baumgartner, Rudolf A</creatorcontrib><creatorcontrib>Albers, David S</creatorcontrib><creatorcontrib>Stamer, W Daniel</creatorcontrib><title>Trabodenoson, an Adenosine Mimetic With A1 Receptor Selectivity Lowers Intraocular Pressure by Increasing Conventional Outflow Facility in Mice</title><title>Investigative ophthalmology & visual science</title><addtitle>Invest Ophthalmol Vis Sci</addtitle><description>To evaluate the relationship between the IOP-lowering effect of trabodenoson and the associated structural and functional changes in the trabecular meshwork (TM).
Six independent cohorts of young and aged mice were exposed to three different topical once-a-day formulations of trabodenoson and eyes were compared to those treated with placebo drops. IOP was measured daily just before drug administration using rebound tonometry. Outflow facility was measured in enucleated eyes. Flow patterns and morphology of conventional outflow tissues were monitored using tracer beads and standard histology, respectively. In parallel, three-dimensional human TM tissue constructs (3D-HTM) were grown and used in experiments to test effect of trabodenoson on the expression of collagen IV, fibronectin, matrix metalloproteinase (MMP)-2 and MMP-14 plus MMP-2 activity.
Topical administration of trabodenoson significantly lowered IOP on every day tested, up to 7 days. After 2 days of treatment, outflow facility increased by 26% in aged mice and 30% overall (young and aged mice), which was significantly different from vehicle (P < 0.05). Outflow facility was 15% higher than controls after 7 days of treatment (P = 0.07). While gross morphology was not affected by treatment, the intensity of tracer bead distribution increased by day 7 (P = 0.05). Parallel experiments in 3D-HTM showed that trabodenoson treatment significantly increased MMP-2 activity and MMP-14 abundance, while decreasing fibronectin and collagen IV expression.
Trabodenoson alters ECM turnover by TM cells and increases conventional outflow facility, which accounts for its ability to lower IOP in young and aged mice.</description><subject>Adenosine - pharmacology</subject><subject>Administration, Ophthalmic</subject><subject>Animals</subject><subject>Antihypertensive Agents - pharmacology</subject><subject>Aqueous Humor - secretion</subject><subject>Biomimetics</subject><subject>Blotting, Western</subject><subject>Cell Line</subject><subject>Collagen Type IV - metabolism</subject><subject>Fibronectins - metabolism</subject><subject>Humans</subject><subject>Immunohistochemistry</subject><subject>Intraocular Pressure - drug effects</subject><subject>Luminescent Measurements</subject><subject>Matrix Metalloproteinase 14 - metabolism</subject><subject>Matrix Metalloproteinase 2 - metabolism</subject><subject>Mice</subject><subject>Mice, Inbred C57BL</subject><subject>Microscopy, Confocal</subject><subject>Nitrates - pharmacology</subject><subject>Physiology and Pharmacology</subject><subject>Purines - pharmacology</subject><subject>Receptor, Adenosine A1 - metabolism</subject><subject>Tissue Scaffolds</subject><subject>Tonometry, Ocular</subject><subject>Trabecular Meshwork - drug effects</subject><subject>Trabecular Meshwork - metabolism</subject><issn>0146-0404</issn><issn>1552-5783</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVkcFOGzEQhi0EatK0R66VjxxYsL32OntBiiJoIwUF0VQ9rmzvLBg5dmp7g_IUfWWWNkXlMqP5Z_T9oxmETim5oLSSlzbs0gWVBSsZZUdoTIVghZDT8hiNCeVVQTjhI_QxpSdCGKWMfEAjVpe8mhI-Rr_XUenQgg8p-HOsPJ79KawHfGs3kK3BP21-xDOK78HANoeIv4MDk-3O5j1ehmeICS98jiqY3qmI7yKk1EfAej_oJoIacA94HvwOfLbBK4dXfe5ceMY3ylj3yrF-8DPwCZ10yiX4fMgT9OPmej3_VixXXxfz2bLYMkZY0XakpUKb1shWiqo2wjClaGsolWoIZDgAZ8CrTmlgnZZKVwSMrnULdVV15QRd_eVue72B1sDr_q7ZRrtRcd8EZZv3HW8fm4ewa4SUnAkxAM4OgBh-9ZBys7HJgHPKQ-hTQ-tpLWohOB1Gv_zv9Wby7wvlC5jcjpI</recordid><startdate>20180101</startdate><enddate>20180101</enddate><creator>Li, Guorong</creator><creator>Torrejon, Karen Y</creator><creator>Unser, Andrea M</creator><creator>Ahmed, Feryan</creator><creator>Navarro, Iris D</creator><creator>Baumgartner, Rudolf A</creator><creator>Albers, David S</creator><creator>Stamer, W Daniel</creator><general>The Association for Research in Vision and Ophthalmology</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20180101</creationdate><title>Trabodenoson, an Adenosine Mimetic With A1 Receptor Selectivity Lowers Intraocular Pressure by Increasing Conventional Outflow Facility in Mice</title><author>Li, Guorong ; Torrejon, Karen Y ; Unser, Andrea M ; Ahmed, Feryan ; Navarro, Iris D ; Baumgartner, Rudolf A ; Albers, David S ; Stamer, W Daniel</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p2202-df0d15bcdc7d7569c5c2aa1dc117ac11078342e46fabe2fb7ab60ecb9bde966f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Adenosine - pharmacology</topic><topic>Administration, Ophthalmic</topic><topic>Animals</topic><topic>Antihypertensive Agents - pharmacology</topic><topic>Aqueous Humor - secretion</topic><topic>Biomimetics</topic><topic>Blotting, Western</topic><topic>Cell Line</topic><topic>Collagen Type IV - metabolism</topic><topic>Fibronectins - metabolism</topic><topic>Humans</topic><topic>Immunohistochemistry</topic><topic>Intraocular Pressure - drug effects</topic><topic>Luminescent Measurements</topic><topic>Matrix Metalloproteinase 14 - metabolism</topic><topic>Matrix Metalloproteinase 2 - metabolism</topic><topic>Mice</topic><topic>Mice, Inbred C57BL</topic><topic>Microscopy, Confocal</topic><topic>Nitrates - pharmacology</topic><topic>Physiology and Pharmacology</topic><topic>Purines - pharmacology</topic><topic>Receptor, Adenosine A1 - metabolism</topic><topic>Tissue Scaffolds</topic><topic>Tonometry, Ocular</topic><topic>Trabecular Meshwork - drug effects</topic><topic>Trabecular Meshwork - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Li, Guorong</creatorcontrib><creatorcontrib>Torrejon, Karen Y</creatorcontrib><creatorcontrib>Unser, Andrea M</creatorcontrib><creatorcontrib>Ahmed, Feryan</creatorcontrib><creatorcontrib>Navarro, Iris D</creatorcontrib><creatorcontrib>Baumgartner, Rudolf A</creatorcontrib><creatorcontrib>Albers, David S</creatorcontrib><creatorcontrib>Stamer, W Daniel</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Investigative ophthalmology & visual science</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Li, Guorong</au><au>Torrejon, Karen Y</au><au>Unser, Andrea M</au><au>Ahmed, Feryan</au><au>Navarro, Iris D</au><au>Baumgartner, Rudolf A</au><au>Albers, David S</au><au>Stamer, W Daniel</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Trabodenoson, an Adenosine Mimetic With A1 Receptor Selectivity Lowers Intraocular Pressure by Increasing Conventional Outflow Facility in Mice</atitle><jtitle>Investigative ophthalmology & visual science</jtitle><addtitle>Invest Ophthalmol Vis Sci</addtitle><date>2018-01-01</date><risdate>2018</risdate><volume>59</volume><issue>1</issue><spage>383</spage><epage>392</epage><pages>383-392</pages><issn>0146-0404</issn><eissn>1552-5783</eissn><abstract>To evaluate the relationship between the IOP-lowering effect of trabodenoson and the associated structural and functional changes in the trabecular meshwork (TM).
Six independent cohorts of young and aged mice were exposed to three different topical once-a-day formulations of trabodenoson and eyes were compared to those treated with placebo drops. IOP was measured daily just before drug administration using rebound tonometry. Outflow facility was measured in enucleated eyes. Flow patterns and morphology of conventional outflow tissues were monitored using tracer beads and standard histology, respectively. In parallel, three-dimensional human TM tissue constructs (3D-HTM) were grown and used in experiments to test effect of trabodenoson on the expression of collagen IV, fibronectin, matrix metalloproteinase (MMP)-2 and MMP-14 plus MMP-2 activity.
Topical administration of trabodenoson significantly lowered IOP on every day tested, up to 7 days. After 2 days of treatment, outflow facility increased by 26% in aged mice and 30% overall (young and aged mice), which was significantly different from vehicle (P < 0.05). Outflow facility was 15% higher than controls after 7 days of treatment (P = 0.07). While gross morphology was not affected by treatment, the intensity of tracer bead distribution increased by day 7 (P = 0.05). Parallel experiments in 3D-HTM showed that trabodenoson treatment significantly increased MMP-2 activity and MMP-14 abundance, while decreasing fibronectin and collagen IV expression.
Trabodenoson alters ECM turnover by TM cells and increases conventional outflow facility, which accounts for its ability to lower IOP in young and aged mice.</abstract><cop>United States</cop><pub>The Association for Research in Vision and Ophthalmology</pub><pmid>29346804</pmid><doi>10.1167/iovs.17-23212</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record> |
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source | MEDLINE; DOAJ Directory of Open Access Journals; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central |
subjects | Adenosine - pharmacology Administration, Ophthalmic Animals Antihypertensive Agents - pharmacology Aqueous Humor - secretion Biomimetics Blotting, Western Cell Line Collagen Type IV - metabolism Fibronectins - metabolism Humans Immunohistochemistry Intraocular Pressure - drug effects Luminescent Measurements Matrix Metalloproteinase 14 - metabolism Matrix Metalloproteinase 2 - metabolism Mice Mice, Inbred C57BL Microscopy, Confocal Nitrates - pharmacology Physiology and Pharmacology Purines - pharmacology Receptor, Adenosine A1 - metabolism Tissue Scaffolds Tonometry, Ocular Trabecular Meshwork - drug effects Trabecular Meshwork - metabolism |
title | Trabodenoson, an Adenosine Mimetic With A1 Receptor Selectivity Lowers Intraocular Pressure by Increasing Conventional Outflow Facility in Mice |
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