Comparison of the Early Effects of Brimonidine and Apraclonidine as Topical Ocular Hypotensive Agents
OBJECTIVE To compare the mechanism of action of short-term administration of brimonidine tartrate and apraclonidine hydrochloride as topical ocular hypotensive agents. SUBJECTS AND METHODS Two randomized, double-masked, placebo-controlled studies of 19 normal human subjects were carried out. The fir...
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Veröffentlicht in: | Archives of ophthalmology (1960) 1999-05, Vol.117 (5), p.586-591 |
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description | OBJECTIVE To compare the mechanism of action of short-term administration of brimonidine tartrate and apraclonidine hydrochloride as topical ocular hypotensive agents. SUBJECTS AND METHODS Two randomized, double-masked, placebo-controlled studies of 19 normal human subjects were carried out. The first study compared brimonidine with apraclonidine in timolol maleate–treated eyes, and the second study compared latanoprost with placebo in timolol-treated eyes. The rate of aqueous flow and intraocular pressure were measured in both studies. The topical drug combinations were instilled the night before and repeated the morning before the measurements. Aqueous humor flow was measured by the rate of disappearance of topically applied fluorescein. Intraocular pressure was measured by pneumatonometry every 2 hours from 8:15 AM to 4:15 PM. RESULTS Both brimonidine and apraclonidine further reduced aqueous flow in timolol-treated eyes from 1.23±0.21 µL/min to 0.96±0.16 µL/min and 0.98±0.17 µL/min, respectively. Consistent reductions were observed in intraocular pressure, with average reductions of 19% with brimonidine and 17% with apraclonidine. Latanoprost had no effect on aqueous flow in timolol-treated eyes (P=.15), but showed an average reduction in intraocular pressure of 13%. CONCLUSIONS Brimonidine and apraclonidine are similar in their effects on the aqueous system. Both reduce intraocular pressure in the timolol-treated eye, primarily, if not exclusively, by further suppressing aqueous flow. In contrast, latanoprost reduces intraocular pressure in the timolol-treated eye without affecting aqueous flow.Arch Ophthalmol 1999;117:586-591--> |
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SUBJECTS AND METHODS Two randomized, double-masked, placebo-controlled studies of 19 normal human subjects were carried out. The first study compared brimonidine with apraclonidine in timolol maleate–treated eyes, and the second study compared latanoprost with placebo in timolol-treated eyes. The rate of aqueous flow and intraocular pressure were measured in both studies. The topical drug combinations were instilled the night before and repeated the morning before the measurements. Aqueous humor flow was measured by the rate of disappearance of topically applied fluorescein. Intraocular pressure was measured by pneumatonometry every 2 hours from 8:15 AM to 4:15 PM. RESULTS Both brimonidine and apraclonidine further reduced aqueous flow in timolol-treated eyes from 1.23±0.21 µL/min to 0.96±0.16 µL/min and 0.98±0.17 µL/min, respectively. Consistent reductions were observed in intraocular pressure, with average reductions of 19% with brimonidine and 17% with apraclonidine. Latanoprost had no effect on aqueous flow in timolol-treated eyes (P=.15), but showed an average reduction in intraocular pressure of 13%. CONCLUSIONS Brimonidine and apraclonidine are similar in their effects on the aqueous system. Both reduce intraocular pressure in the timolol-treated eye, primarily, if not exclusively, by further suppressing aqueous flow. In contrast, latanoprost reduces intraocular pressure in the timolol-treated eye without affecting aqueous flow.Arch Ophthalmol 1999;117:586-591--></description><identifier>ISSN: 0003-9950</identifier><identifier>ISSN: 2168-6165</identifier><identifier>EISSN: 1538-3601</identifier><identifier>EISSN: 2168-6173</identifier><identifier>DOI: 10.1001/archopht.117.5.586</identifier><identifier>PMID: 10326954</identifier><language>eng</language><publisher>Chicago, IL: American Medical Association</publisher><subject><![CDATA[Administration, Topical ; Adrenergic alpha-Agonists - administration & dosage ; Adrenergic alpha-Agonists - pharmacology ; Antihypertensive Agents - administration & dosage ; Antihypertensive Agents - pharmacology ; Aqueous Humor - metabolism ; Biological and medical sciences ; Brimonidine Tartrate ; Clonidine - administration & dosage ; Clonidine - analogs & derivatives ; Clonidine - pharmacology ; Double-Blind Method ; Drug Synergism ; Drug Therapy, Combination ; Eye ; Fluorophotometry ; Humans ; Intraocular Pressure - drug effects ; Latanoprost ; Medical sciences ; Ophthalmic Solutions - administration & dosage ; Ophthalmic Solutions - pharmacology ; Pharmacology. Drug treatments ; Prostaglandins F, Synthetic - administration & dosage ; Prostaglandins F, Synthetic - pharmacology ; Quinoxalines - administration & dosage ; Quinoxalines - pharmacology ; Timolol - administration & dosage ; Timolol - pharmacology]]></subject><ispartof>Archives of ophthalmology (1960), 1999-05, Vol.117 (5), p.586-591</ispartof><rights>1999 INIST-CNRS</rights><rights>Copyright American Medical Association May 1999</rights><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a483t-5f8ae68510d7e8b62353df4e64e0e9c71a2cf4a9acca5f713a5494bcf1997e413</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=1804711$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/10326954$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Maus, Todd L</creatorcontrib><creatorcontrib>Nau, Cherie</creatorcontrib><creatorcontrib>Brubaker, Richard F</creatorcontrib><title>Comparison of the Early Effects of Brimonidine and Apraclonidine as Topical Ocular Hypotensive Agents</title><title>Archives of ophthalmology (1960)</title><addtitle>Arch Ophthalmol</addtitle><description>OBJECTIVE To compare the mechanism of action of short-term administration of brimonidine tartrate and apraclonidine hydrochloride as topical ocular hypotensive agents. SUBJECTS AND METHODS Two randomized, double-masked, placebo-controlled studies of 19 normal human subjects were carried out. The first study compared brimonidine with apraclonidine in timolol maleate–treated eyes, and the second study compared latanoprost with placebo in timolol-treated eyes. The rate of aqueous flow and intraocular pressure were measured in both studies. The topical drug combinations were instilled the night before and repeated the morning before the measurements. Aqueous humor flow was measured by the rate of disappearance of topically applied fluorescein. Intraocular pressure was measured by pneumatonometry every 2 hours from 8:15 AM to 4:15 PM. RESULTS Both brimonidine and apraclonidine further reduced aqueous flow in timolol-treated eyes from 1.23±0.21 µL/min to 0.96±0.16 µL/min and 0.98±0.17 µL/min, respectively. Consistent reductions were observed in intraocular pressure, with average reductions of 19% with brimonidine and 17% with apraclonidine. Latanoprost had no effect on aqueous flow in timolol-treated eyes (P=.15), but showed an average reduction in intraocular pressure of 13%. CONCLUSIONS Brimonidine and apraclonidine are similar in their effects on the aqueous system. Both reduce intraocular pressure in the timolol-treated eye, primarily, if not exclusively, by further suppressing aqueous flow. In contrast, latanoprost reduces intraocular pressure in the timolol-treated eye without affecting aqueous flow.Arch Ophthalmol 1999;117:586-591--></description><subject>Administration, Topical</subject><subject>Adrenergic alpha-Agonists - administration & dosage</subject><subject>Adrenergic alpha-Agonists - pharmacology</subject><subject>Antihypertensive Agents - administration & dosage</subject><subject>Antihypertensive Agents - pharmacology</subject><subject>Aqueous Humor - metabolism</subject><subject>Biological and medical sciences</subject><subject>Brimonidine Tartrate</subject><subject>Clonidine - administration & dosage</subject><subject>Clonidine - analogs & derivatives</subject><subject>Clonidine - pharmacology</subject><subject>Double-Blind Method</subject><subject>Drug Synergism</subject><subject>Drug Therapy, Combination</subject><subject>Eye</subject><subject>Fluorophotometry</subject><subject>Humans</subject><subject>Intraocular Pressure - drug effects</subject><subject>Latanoprost</subject><subject>Medical sciences</subject><subject>Ophthalmic Solutions - administration & dosage</subject><subject>Ophthalmic Solutions - pharmacology</subject><subject>Pharmacology. Drug treatments</subject><subject>Prostaglandins F, Synthetic - administration & dosage</subject><subject>Prostaglandins F, Synthetic - pharmacology</subject><subject>Quinoxalines - administration & dosage</subject><subject>Quinoxalines - pharmacology</subject><subject>Timolol - administration & dosage</subject><subject>Timolol - pharmacology</subject><issn>0003-9950</issn><issn>2168-6165</issn><issn>1538-3601</issn><issn>2168-6173</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1999</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpNkMFuEzEQhi0EomnhAeCALNTrBs_a3rWPIQoUqVIv5WxNvGOy1Wa92JtKeXscJRROlsffPzP-GPsIYglCwBdMfhen3bwEaJd6qU3zii1AS1PJRsBrthBCyMpaLa7Ydc5P5dqAsG_ZFQhZN1arBaN13E-Y-hxHHgOfd8Q3mIYj34RAfs6n4tfU7-PYd_1IHMeOr6aEfnipZP4Yp97jwB_8YcDE745TnGnM_TPx1S8a5_yOvQk4ZHp_OW_Yz2-bx_Vddf_w_cd6dV-hMnKudDBIjdEgupbMtqmlll1Q1CgSZH0LWPug0KL3qEMLErWyausDWNuSAnnDPp_7Tin-PlCe3VM8pLGMdLUE24jWqgLVZ8inmHOi4KbyQUxHB8KdxLq_Yl0R67QrYkvo06XzYbun7r_I2WQBbi8A5uIiJBx9n_9xRqgWTht-OGO4x5dHBWCkkX8ANnSLsQ</recordid><startdate>19990501</startdate><enddate>19990501</enddate><creator>Maus, Todd L</creator><creator>Nau, Cherie</creator><creator>Brubaker, Richard F</creator><general>American Medical Association</general><scope>IQODW</scope><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>7TK</scope><scope>K9.</scope><scope>NAPCQ</scope></search><sort><creationdate>19990501</creationdate><title>Comparison of the Early Effects of Brimonidine and Apraclonidine as Topical Ocular Hypotensive Agents</title><author>Maus, Todd L ; Nau, Cherie ; Brubaker, Richard F</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a483t-5f8ae68510d7e8b62353df4e64e0e9c71a2cf4a9acca5f713a5494bcf1997e413</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1999</creationdate><topic>Administration, Topical</topic><topic>Adrenergic alpha-Agonists - administration & dosage</topic><topic>Adrenergic alpha-Agonists - pharmacology</topic><topic>Antihypertensive Agents - administration & dosage</topic><topic>Antihypertensive Agents - pharmacology</topic><topic>Aqueous Humor - metabolism</topic><topic>Biological and medical sciences</topic><topic>Brimonidine Tartrate</topic><topic>Clonidine - administration & dosage</topic><topic>Clonidine - analogs & derivatives</topic><topic>Clonidine - pharmacology</topic><topic>Double-Blind Method</topic><topic>Drug Synergism</topic><topic>Drug Therapy, Combination</topic><topic>Eye</topic><topic>Fluorophotometry</topic><topic>Humans</topic><topic>Intraocular Pressure - drug effects</topic><topic>Latanoprost</topic><topic>Medical sciences</topic><topic>Ophthalmic Solutions - administration & dosage</topic><topic>Ophthalmic Solutions - pharmacology</topic><topic>Pharmacology. Drug treatments</topic><topic>Prostaglandins F, Synthetic - administration & dosage</topic><topic>Prostaglandins F, Synthetic - pharmacology</topic><topic>Quinoxalines - administration & dosage</topic><topic>Quinoxalines - pharmacology</topic><topic>Timolol - administration & dosage</topic><topic>Timolol - pharmacology</topic><toplevel>online_resources</toplevel><creatorcontrib>Maus, Todd L</creatorcontrib><creatorcontrib>Nau, Cherie</creatorcontrib><creatorcontrib>Brubaker, Richard F</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Neurosciences Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Premium</collection><jtitle>Archives of ophthalmology (1960)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Maus, Todd L</au><au>Nau, Cherie</au><au>Brubaker, Richard F</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Comparison of the Early Effects of Brimonidine and Apraclonidine as Topical Ocular Hypotensive Agents</atitle><jtitle>Archives of ophthalmology (1960)</jtitle><addtitle>Arch Ophthalmol</addtitle><date>1999-05-01</date><risdate>1999</risdate><volume>117</volume><issue>5</issue><spage>586</spage><epage>591</epage><pages>586-591</pages><issn>0003-9950</issn><issn>2168-6165</issn><eissn>1538-3601</eissn><eissn>2168-6173</eissn><abstract>OBJECTIVE To compare the mechanism of action of short-term administration of brimonidine tartrate and apraclonidine hydrochloride as topical ocular hypotensive agents. SUBJECTS AND METHODS Two randomized, double-masked, placebo-controlled studies of 19 normal human subjects were carried out. The first study compared brimonidine with apraclonidine in timolol maleate–treated eyes, and the second study compared latanoprost with placebo in timolol-treated eyes. The rate of aqueous flow and intraocular pressure were measured in both studies. The topical drug combinations were instilled the night before and repeated the morning before the measurements. Aqueous humor flow was measured by the rate of disappearance of topically applied fluorescein. Intraocular pressure was measured by pneumatonometry every 2 hours from 8:15 AM to 4:15 PM. RESULTS Both brimonidine and apraclonidine further reduced aqueous flow in timolol-treated eyes from 1.23±0.21 µL/min to 0.96±0.16 µL/min and 0.98±0.17 µL/min, respectively. Consistent reductions were observed in intraocular pressure, with average reductions of 19% with brimonidine and 17% with apraclonidine. Latanoprost had no effect on aqueous flow in timolol-treated eyes (P=.15), but showed an average reduction in intraocular pressure of 13%. CONCLUSIONS Brimonidine and apraclonidine are similar in their effects on the aqueous system. Both reduce intraocular pressure in the timolol-treated eye, primarily, if not exclusively, by further suppressing aqueous flow. In contrast, latanoprost reduces intraocular pressure in the timolol-treated eye without affecting aqueous flow.Arch Ophthalmol 1999;117:586-591--></abstract><cop>Chicago, IL</cop><pub>American Medical Association</pub><pmid>10326954</pmid><doi>10.1001/archopht.117.5.586</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Administration, Topical Adrenergic alpha-Agonists - administration & dosage Adrenergic alpha-Agonists - pharmacology Antihypertensive Agents - administration & dosage Antihypertensive Agents - pharmacology Aqueous Humor - metabolism Biological and medical sciences Brimonidine Tartrate Clonidine - administration & dosage Clonidine - analogs & derivatives Clonidine - pharmacology Double-Blind Method Drug Synergism Drug Therapy, Combination Eye Fluorophotometry Humans Intraocular Pressure - drug effects Latanoprost Medical sciences Ophthalmic Solutions - administration & dosage Ophthalmic Solutions - pharmacology Pharmacology. Drug treatments Prostaglandins F, Synthetic - administration & dosage Prostaglandins F, Synthetic - pharmacology Quinoxalines - administration & dosage Quinoxalines - pharmacology Timolol - administration & dosage Timolol - pharmacology |
title | Comparison of the Early Effects of Brimonidine and Apraclonidine as Topical Ocular Hypotensive Agents |
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