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Topical aminocaproic acid facilitates reepithelialization of persistent epithelial defects

Purpose. After corneal injury, persistent epithelial defects (PED's) may occur due to the chronic failure of the regenerating epithelium to adhere to the underlying stroma. The aim of this study was to examine the potential of epsilon-aminocaproic acid (EACA) as a topical treatment for PED'...

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Published in:Current eye research 1999-02, Vol.18 (2), p.150-157
Main Authors: Williams, Patricia B., Crouch, Earl R., Crouch, Eric R., Mazaheri, Mehrdad
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container_title Current eye research
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creator Williams, Patricia B.
Crouch, Earl R.
Crouch, Eric R.
Mazaheri, Mehrdad
description Purpose. After corneal injury, persistent epithelial defects (PED's) may occur due to the chronic failure of the regenerating epithelium to adhere to the underlying stroma. The aim of this study was to examine the potential of epsilon-aminocaproic acid (EACA) as a topical treatment for PED's. EACA inhibits the activation of plasmin, which metabolizes fibronectin. Fibronectin, a glycoprotein, anchors corneal epithelium to the basement membrane and the underlying stroma. Methods. In anesthetized rabbits, PED's were induced with sodium hydroxide (1 N). Seven days later, during the late healing phase, treatment began with administration of EACA (30%) to the right eye and administration of vehicle alone to the left eye three times daily. A control group received neither EACA nor vehicle. Rabbits were treated for 19 days. PED's were visualized by fluorescein staining. Their size was mapped using digital planimetry. Results. After 11 days of treatment with EACA, treated PED's were 50% smaller than in corneas treated with vehicle alone. Following treatment for 15 days, corneas treated with EACA had significantly greater re-epithelialization than vehicle-treated or control corneas. Frozen sections stained immunofluorescently for fibronectin appeared to qualitatively contain more adherent fibronectin in treated corneas. Transmission and scanning electron microscopy indicated that the epithelium was more polymorphic, thinner and vacuolated in untreated controls compared to EACA treated eyes. Light microscopy demonstrated more continuous adherent epithelium after EACA treatment. Conclusions. Topically administered EACA decreases both the severity and incidence of persistent epithelial defects produced by alkali burns to the cornea. EACA appears to promote adherence of the regenerating epithelium to the underlying stroma. Thus, topically administered EACA may be an effective treatment for this chronic condition.
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After corneal injury, persistent epithelial defects (PED's) may occur due to the chronic failure of the regenerating epithelium to adhere to the underlying stroma. The aim of this study was to examine the potential of epsilon-aminocaproic acid (EACA) as a topical treatment for PED's. EACA inhibits the activation of plasmin, which metabolizes fibronectin. Fibronectin, a glycoprotein, anchors corneal epithelium to the basement membrane and the underlying stroma. Methods. In anesthetized rabbits, PED's were induced with sodium hydroxide (1 N). Seven days later, during the late healing phase, treatment began with administration of EACA (30%) to the right eye and administration of vehicle alone to the left eye three times daily. A control group received neither EACA nor vehicle. Rabbits were treated for 19 days. PED's were visualized by fluorescein staining. Their size was mapped using digital planimetry. Results. After 11 days of treatment with EACA, treated PED's were 50% smaller than in corneas treated with vehicle alone. Following treatment for 15 days, corneas treated with EACA had significantly greater re-epithelialization than vehicle-treated or control corneas. Frozen sections stained immunofluorescently for fibronectin appeared to qualitatively contain more adherent fibronectin in treated corneas. Transmission and scanning electron microscopy indicated that the epithelium was more polymorphic, thinner and vacuolated in untreated controls compared to EACA treated eyes. Light microscopy demonstrated more continuous adherent epithelium after EACA treatment. Conclusions. Topically administered EACA decreases both the severity and incidence of persistent epithelial defects produced by alkali burns to the cornea. EACA appears to promote adherence of the regenerating epithelium to the underlying stroma. Thus, topically administered EACA may be an effective treatment for this chronic condition.</description><identifier>ISSN: 0271-3683</identifier><identifier>EISSN: 1460-2202</identifier><identifier>DOI: 10.1076/ceyr.18.2.150.5382</identifier><identifier>PMID: 10223660</identifier><language>eng</language><publisher>England: Informa UK Ltd</publisher><subject>Administration, Topical ; Aminocaproic Acid - administration &amp; dosage ; Aminocaproic Acid - therapeutic use ; Animals ; Antifibrinolytic Agents - administration &amp; dosage ; Antifibrinolytic Agents - therapeutic use ; Burns, Chemical - drug therapy ; Burns, Chemical - metabolism ; Burns, Chemical - pathology ; Cell Adhesion - drug effects ; Corneal Diseases - drug therapy ; Corneal Diseases - metabolism ; Corneal Diseases - pathology ; Epithelium, Corneal - metabolism ; Epithelium, Corneal - physiology ; Epithelium, Corneal - ultrastructure ; Eye Burns - chemically induced ; Eye Burns - metabolism ; Eye Burns - pathology ; Female ; Fibronectins - metabolism ; Fluorescent Antibody Technique, Indirect ; Microscopy, Fluorescence ; Rabbits ; Regeneration - drug effects ; Sodium Hydroxide ; Wound Healing - drug effects</subject><ispartof>Current eye research, 1999-02, Vol.18 (2), p.150-157</ispartof><rights>1999 Informa UK Ltd All rights reserved: reproduction in whole or part not permitted 1999</rights><rights>Copyright Swets &amp; Zeitlinger bv Feb 1999</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c433t-420f1e58483196b24bf5ca589c5d1c03bbd8fb0a18ed174e4a665caa6ecdf9ce3</citedby><cites>FETCH-LOGICAL-c433t-420f1e58483196b24bf5ca589c5d1c03bbd8fb0a18ed174e4a665caa6ecdf9ce3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27923,27924</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/10223660$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Williams, Patricia B.</creatorcontrib><creatorcontrib>Crouch, Earl R.</creatorcontrib><creatorcontrib>Crouch, Eric R.</creatorcontrib><creatorcontrib>Mazaheri, Mehrdad</creatorcontrib><title>Topical aminocaproic acid facilitates reepithelialization of persistent epithelial defects</title><title>Current eye research</title><addtitle>Curr Eye Res</addtitle><description>Purpose. After corneal injury, persistent epithelial defects (PED's) may occur due to the chronic failure of the regenerating epithelium to adhere to the underlying stroma. The aim of this study was to examine the potential of epsilon-aminocaproic acid (EACA) as a topical treatment for PED's. EACA inhibits the activation of plasmin, which metabolizes fibronectin. Fibronectin, a glycoprotein, anchors corneal epithelium to the basement membrane and the underlying stroma. Methods. In anesthetized rabbits, PED's were induced with sodium hydroxide (1 N). Seven days later, during the late healing phase, treatment began with administration of EACA (30%) to the right eye and administration of vehicle alone to the left eye three times daily. A control group received neither EACA nor vehicle. Rabbits were treated for 19 days. PED's were visualized by fluorescein staining. Their size was mapped using digital planimetry. Results. After 11 days of treatment with EACA, treated PED's were 50% smaller than in corneas treated with vehicle alone. Following treatment for 15 days, corneas treated with EACA had significantly greater re-epithelialization than vehicle-treated or control corneas. Frozen sections stained immunofluorescently for fibronectin appeared to qualitatively contain more adherent fibronectin in treated corneas. Transmission and scanning electron microscopy indicated that the epithelium was more polymorphic, thinner and vacuolated in untreated controls compared to EACA treated eyes. Light microscopy demonstrated more continuous adherent epithelium after EACA treatment. Conclusions. Topically administered EACA decreases both the severity and incidence of persistent epithelial defects produced by alkali burns to the cornea. EACA appears to promote adherence of the regenerating epithelium to the underlying stroma. Thus, topically administered EACA may be an effective treatment for this chronic condition.</description><subject>Administration, Topical</subject><subject>Aminocaproic Acid - administration &amp; dosage</subject><subject>Aminocaproic Acid - therapeutic use</subject><subject>Animals</subject><subject>Antifibrinolytic Agents - administration &amp; dosage</subject><subject>Antifibrinolytic Agents - therapeutic use</subject><subject>Burns, Chemical - drug therapy</subject><subject>Burns, Chemical - metabolism</subject><subject>Burns, Chemical - pathology</subject><subject>Cell Adhesion - drug effects</subject><subject>Corneal Diseases - drug therapy</subject><subject>Corneal Diseases - metabolism</subject><subject>Corneal Diseases - pathology</subject><subject>Epithelium, Corneal - metabolism</subject><subject>Epithelium, Corneal - physiology</subject><subject>Epithelium, Corneal - ultrastructure</subject><subject>Eye Burns - chemically induced</subject><subject>Eye Burns - metabolism</subject><subject>Eye Burns - pathology</subject><subject>Female</subject><subject>Fibronectins - metabolism</subject><subject>Fluorescent Antibody Technique, Indirect</subject><subject>Microscopy, Fluorescence</subject><subject>Rabbits</subject><subject>Regeneration - drug effects</subject><subject>Sodium Hydroxide</subject><subject>Wound Healing - drug effects</subject><issn>0271-3683</issn><issn>1460-2202</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1999</creationdate><recordtype>article</recordtype><recordid>eNp9kE1LAzEQhoMoWj_-gAdZvO-aj900BT1I8QsKXvTiJcxmJzSy3axJitRf75YWrAe9ZCB53pnMQ8g5owWjY3llcBUKpgpesIoWlVB8j4xYKWnOOeX7ZET5mOVCKnFEjmN8p3R9UR6SI0Y5F1LSEXl78b0z0GawcJ030AfvTAbGNZkdztYlSBizgNi7NMfWQeu-IDnfZd5mPYboYsIuZT_vWYMWTYqn5MBCG_FsW0_I6_3dy_Qxnz0_PE1vZ7kphUh5yallWKlSCTaRNS9rWxmo1MRUDTNU1HWjbE2BKWzYuMQSpBwAkGgaOzEoTsjlpu_w948lxqTf_TJ0w0jNJhXnjAs1QHwDmeBjDGh1H9wCwkozqtc29dqmZkpzPdjUa5tD6GLbeVkvsNmJbPQNwM0GcJ31YQGfPrSNTrBqfbABOuOiFv8OuP6VnyO0aW4g4M4Of8e_AdB4nKc</recordid><startdate>19990201</startdate><enddate>19990201</enddate><creator>Williams, Patricia B.</creator><creator>Crouch, Earl R.</creator><creator>Crouch, Eric R.</creator><creator>Mazaheri, Mehrdad</creator><general>Informa UK Ltd</general><general>Taylor &amp; 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After corneal injury, persistent epithelial defects (PED's) may occur due to the chronic failure of the regenerating epithelium to adhere to the underlying stroma. The aim of this study was to examine the potential of epsilon-aminocaproic acid (EACA) as a topical treatment for PED's. EACA inhibits the activation of plasmin, which metabolizes fibronectin. Fibronectin, a glycoprotein, anchors corneal epithelium to the basement membrane and the underlying stroma. Methods. In anesthetized rabbits, PED's were induced with sodium hydroxide (1 N). Seven days later, during the late healing phase, treatment began with administration of EACA (30%) to the right eye and administration of vehicle alone to the left eye three times daily. A control group received neither EACA nor vehicle. Rabbits were treated for 19 days. PED's were visualized by fluorescein staining. Their size was mapped using digital planimetry. Results. After 11 days of treatment with EACA, treated PED's were 50% smaller than in corneas treated with vehicle alone. Following treatment for 15 days, corneas treated with EACA had significantly greater re-epithelialization than vehicle-treated or control corneas. Frozen sections stained immunofluorescently for fibronectin appeared to qualitatively contain more adherent fibronectin in treated corneas. Transmission and scanning electron microscopy indicated that the epithelium was more polymorphic, thinner and vacuolated in untreated controls compared to EACA treated eyes. Light microscopy demonstrated more continuous adherent epithelium after EACA treatment. Conclusions. Topically administered EACA decreases both the severity and incidence of persistent epithelial defects produced by alkali burns to the cornea. EACA appears to promote adherence of the regenerating epithelium to the underlying stroma. Thus, topically administered EACA may be an effective treatment for this chronic condition.</abstract><cop>England</cop><pub>Informa UK Ltd</pub><pmid>10223660</pmid><doi>10.1076/ceyr.18.2.150.5382</doi><tpages>8</tpages></addata></record>
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subjects Administration, Topical
Aminocaproic Acid - administration & dosage
Aminocaproic Acid - therapeutic use
Animals
Antifibrinolytic Agents - administration & dosage
Antifibrinolytic Agents - therapeutic use
Burns, Chemical - drug therapy
Burns, Chemical - metabolism
Burns, Chemical - pathology
Cell Adhesion - drug effects
Corneal Diseases - drug therapy
Corneal Diseases - metabolism
Corneal Diseases - pathology
Epithelium, Corneal - metabolism
Epithelium, Corneal - physiology
Epithelium, Corneal - ultrastructure
Eye Burns - chemically induced
Eye Burns - metabolism
Eye Burns - pathology
Female
Fibronectins - metabolism
Fluorescent Antibody Technique, Indirect
Microscopy, Fluorescence
Rabbits
Regeneration - drug effects
Sodium Hydroxide
Wound Healing - drug effects
title Topical aminocaproic acid facilitates reepithelialization of persistent epithelial defects
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