Assessment of Anticollagenase Treatments After Insertion of a Keratoprosthetic Material in the Rabbit Cornea
PURPOSEThis study was performed to evaluate the enzyme production in response to implantation of the hydrogel material used in the experimental Chirila keratoprosthesis (KPro) and to assess the effects of five topical drugs on enzyme production and activity. KPros may be extruded from the cornea as...
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Veröffentlicht in: | Cornea 1998-01, Vol.17 (1), p.108-108 |
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description | PURPOSEThis study was performed to evaluate the enzyme production in response to implantation of the hydrogel material used in the experimental Chirila keratoprosthesis (KPro) and to assess the effects of five topical drugs on enzyme production and activity. KPros may be extruded from the cornea as a result of tissue melting, a process that involves excessive enzyme activity. To reduce the possibility of implant loss for the hydrogel Chirila KPro, a number of antiinflammatory drugs that have been used to treat other corneal melting conditions were investigated for their effect on initial collagenase activity after the implantation of KPro material into the rabbit cornea.
METHODSPoly(2-hydroxyethyl methacrylate) sponge pieces were implanted into rabbit corneas. Prednisolone, tetracycline, medroxyprogesterone, acetylcysteine, and sodium citrate were assessed for effects on gelatinolytic activity and stromal collagenase [matrix metalloprotease-1 (MMP-1)] production in vivo and in vitro by using zymography and Western blotting techniques.
RESULTSWhereas all five anticollagenase drugs were effective in reducing gelatinolytic activity in vitro, many were ineffective in vivo. However, medroxyprogesterone caused a reduction of gelatinolytic activity in vivo. The amount of MMP-1, as measured by immunoblotting, also was reduced by medroxyprogesterone treatment when compared with untreated controls. An increase in the apparent molecular weight of MMP-1 in operated corneas appears to be the result of the association of MMP-1 with collagen fragments resulting from the surgical trauma.
CONCLUSIONThis study indicates that topical medroxyprogesterone may be a useful adjunctive therapy after prosthokeratoplasty. |
doi_str_mv | 10.1097/00003226-199801000-00016 |
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METHODSPoly(2-hydroxyethyl methacrylate) sponge pieces were implanted into rabbit corneas. Prednisolone, tetracycline, medroxyprogesterone, acetylcysteine, and sodium citrate were assessed for effects on gelatinolytic activity and stromal collagenase [matrix metalloprotease-1 (MMP-1)] production in vivo and in vitro by using zymography and Western blotting techniques.
RESULTSWhereas all five anticollagenase drugs were effective in reducing gelatinolytic activity in vitro, many were ineffective in vivo. However, medroxyprogesterone caused a reduction of gelatinolytic activity in vivo. The amount of MMP-1, as measured by immunoblotting, also was reduced by medroxyprogesterone treatment when compared with untreated controls. An increase in the apparent molecular weight of MMP-1 in operated corneas appears to be the result of the association of MMP-1 with collagen fragments resulting from the surgical trauma.
CONCLUSIONThis study indicates that topical medroxyprogesterone may be a useful adjunctive therapy after prosthokeratoplasty.</description><identifier>ISSN: 0277-3740</identifier><identifier>EISSN: 1536-4798</identifier><identifier>DOI: 10.1097/00003226-199801000-00016</identifier><identifier>PMID: 9436888</identifier><language>eng</language><publisher>United States: Lippincott-Raven Publishers</publisher><subject>Acetylcysteine - administration & dosage ; Acetylcysteine - pharmacology ; Administration, Topical ; Animals ; Blotting, Western ; Citrates - administration & dosage ; Citrates - pharmacology ; Collagenases - metabolism ; Cornea - drug effects ; Cornea - enzymology ; Cornea - surgery ; Disease Models, Animal ; Electrophoresis, Polyacrylamide Gel ; Gelatinases - metabolism ; Graft Survival ; Implants, Experimental ; Matrix Metalloproteinase Inhibitors ; Medroxyprogesterone - administration & dosage ; Medroxyprogesterone - pharmacology ; Methacrylates ; Ophthalmic Solutions ; Prednisolone - administration & dosage ; Prednisolone - pharmacology ; Rabbits ; Tetracycline - administration & dosage ; Tetracycline - pharmacology ; Treatment Outcome</subject><ispartof>Cornea, 1998-01, Vol.17 (1), p.108-108</ispartof><rights>Lippincott-Raven Publishers.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3556-4182e3d381a75b02638eafb7b0c3f636d92053d7aada10335b19e53176c424c83</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>315,781,785,27929,27930</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9436888$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Fitton, J Helen</creatorcontrib><creatorcontrib>Ziegelaar, Brian W</creatorcontrib><creatorcontrib>Hicks, Celia R</creatorcontrib><creatorcontrib>Clayton, Anthony B</creatorcontrib><creatorcontrib>Crawford, Geoffrey J</creatorcontrib><creatorcontrib>Constable, Ian J</creatorcontrib><creatorcontrib>Chirila, Traian V</creatorcontrib><title>Assessment of Anticollagenase Treatments After Insertion of a Keratoprosthetic Material in the Rabbit Cornea</title><title>Cornea</title><addtitle>Cornea</addtitle><description>PURPOSEThis study was performed to evaluate the enzyme production in response to implantation of the hydrogel material used in the experimental Chirila keratoprosthesis (KPro) and to assess the effects of five topical drugs on enzyme production and activity. KPros may be extruded from the cornea as a result of tissue melting, a process that involves excessive enzyme activity. To reduce the possibility of implant loss for the hydrogel Chirila KPro, a number of antiinflammatory drugs that have been used to treat other corneal melting conditions were investigated for their effect on initial collagenase activity after the implantation of KPro material into the rabbit cornea.
METHODSPoly(2-hydroxyethyl methacrylate) sponge pieces were implanted into rabbit corneas. Prednisolone, tetracycline, medroxyprogesterone, acetylcysteine, and sodium citrate were assessed for effects on gelatinolytic activity and stromal collagenase [matrix metalloprotease-1 (MMP-1)] production in vivo and in vitro by using zymography and Western blotting techniques.
RESULTSWhereas all five anticollagenase drugs were effective in reducing gelatinolytic activity in vitro, many were ineffective in vivo. However, medroxyprogesterone caused a reduction of gelatinolytic activity in vivo. The amount of MMP-1, as measured by immunoblotting, also was reduced by medroxyprogesterone treatment when compared with untreated controls. An increase in the apparent molecular weight of MMP-1 in operated corneas appears to be the result of the association of MMP-1 with collagen fragments resulting from the surgical trauma.
CONCLUSIONThis study indicates that topical medroxyprogesterone may be a useful adjunctive therapy after prosthokeratoplasty.</description><subject>Acetylcysteine - administration & dosage</subject><subject>Acetylcysteine - pharmacology</subject><subject>Administration, Topical</subject><subject>Animals</subject><subject>Blotting, Western</subject><subject>Citrates - administration & dosage</subject><subject>Citrates - pharmacology</subject><subject>Collagenases - metabolism</subject><subject>Cornea - drug effects</subject><subject>Cornea - enzymology</subject><subject>Cornea - surgery</subject><subject>Disease Models, Animal</subject><subject>Electrophoresis, Polyacrylamide Gel</subject><subject>Gelatinases - metabolism</subject><subject>Graft Survival</subject><subject>Implants, Experimental</subject><subject>Matrix Metalloproteinase Inhibitors</subject><subject>Medroxyprogesterone - administration & dosage</subject><subject>Medroxyprogesterone - pharmacology</subject><subject>Methacrylates</subject><subject>Ophthalmic Solutions</subject><subject>Prednisolone - administration & dosage</subject><subject>Prednisolone - pharmacology</subject><subject>Rabbits</subject><subject>Tetracycline - administration & dosage</subject><subject>Tetracycline - pharmacology</subject><subject>Treatment Outcome</subject><issn>0277-3740</issn><issn>1536-4798</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1998</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kUtLAzEUhYMotVZ_gpCVu9E8ZpLMshQfxYogdR3uzNyxo_OoSUrx35va6s5ACMk5J7n3CyGUs2vOcn3D4pBCqITnuWE87pI4uToiY55JlaQ6N8dkzITWidQpOyVn3r9Hi9ZKjMgoT6UyxoxJO_Ueve-wD3So6bQPTTm0LbxhDx7p0iGEnejptA7o6Lz36EIz9Ds30Ed0EIa1G3xYYYzSJ4iuBlra9DQe0RcoiibQ2eB6hHNyUkPr8eKwTsjr3e1y9pAsnu_ns-kiKWWWxeK5ESgraTjorGBCSYNQF7pgpayVVFUuWCYrDVABZ1JmBc8xk1yrMhVpaeSEXO3vjYV9btAH2zW-xNhWj8PGW50rJdLIYELM3ljGDrzD2q5d04H7spzZHWj7C9r-gbY_oGP08vDGpuiw-gseyEY93evboY1I_Ee72aKzK4Q2rOx__ye_AftMiMs</recordid><startdate>199801</startdate><enddate>199801</enddate><creator>Fitton, J Helen</creator><creator>Ziegelaar, Brian W</creator><creator>Hicks, Celia R</creator><creator>Clayton, Anthony B</creator><creator>Crawford, Geoffrey J</creator><creator>Constable, Ian J</creator><creator>Chirila, Traian V</creator><general>Lippincott-Raven Publishers</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>199801</creationdate><title>Assessment of Anticollagenase Treatments After Insertion of a Keratoprosthetic Material in the Rabbit Cornea</title><author>Fitton, J Helen ; Ziegelaar, Brian W ; Hicks, Celia R ; Clayton, Anthony B ; Crawford, Geoffrey J ; Constable, Ian J ; Chirila, Traian V</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3556-4182e3d381a75b02638eafb7b0c3f636d92053d7aada10335b19e53176c424c83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1998</creationdate><topic>Acetylcysteine - administration & dosage</topic><topic>Acetylcysteine - pharmacology</topic><topic>Administration, Topical</topic><topic>Animals</topic><topic>Blotting, Western</topic><topic>Citrates - administration & dosage</topic><topic>Citrates - pharmacology</topic><topic>Collagenases - metabolism</topic><topic>Cornea - drug effects</topic><topic>Cornea - enzymology</topic><topic>Cornea - surgery</topic><topic>Disease Models, Animal</topic><topic>Electrophoresis, Polyacrylamide Gel</topic><topic>Gelatinases - metabolism</topic><topic>Graft Survival</topic><topic>Implants, Experimental</topic><topic>Matrix Metalloproteinase Inhibitors</topic><topic>Medroxyprogesterone - administration & dosage</topic><topic>Medroxyprogesterone - pharmacology</topic><topic>Methacrylates</topic><topic>Ophthalmic Solutions</topic><topic>Prednisolone - administration & dosage</topic><topic>Prednisolone - pharmacology</topic><topic>Rabbits</topic><topic>Tetracycline - administration & dosage</topic><topic>Tetracycline - pharmacology</topic><topic>Treatment Outcome</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Fitton, J Helen</creatorcontrib><creatorcontrib>Ziegelaar, Brian W</creatorcontrib><creatorcontrib>Hicks, Celia R</creatorcontrib><creatorcontrib>Clayton, Anthony B</creatorcontrib><creatorcontrib>Crawford, Geoffrey J</creatorcontrib><creatorcontrib>Constable, Ian J</creatorcontrib><creatorcontrib>Chirila, Traian V</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>Cornea</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Fitton, J Helen</au><au>Ziegelaar, Brian W</au><au>Hicks, Celia R</au><au>Clayton, Anthony B</au><au>Crawford, Geoffrey J</au><au>Constable, Ian J</au><au>Chirila, Traian V</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Assessment of Anticollagenase Treatments After Insertion of a Keratoprosthetic Material in the Rabbit Cornea</atitle><jtitle>Cornea</jtitle><addtitle>Cornea</addtitle><date>1998-01</date><risdate>1998</risdate><volume>17</volume><issue>1</issue><spage>108</spage><epage>108</epage><pages>108-108</pages><issn>0277-3740</issn><eissn>1536-4798</eissn><abstract>PURPOSEThis study was performed to evaluate the enzyme production in response to implantation of the hydrogel material used in the experimental Chirila keratoprosthesis (KPro) and to assess the effects of five topical drugs on enzyme production and activity. KPros may be extruded from the cornea as a result of tissue melting, a process that involves excessive enzyme activity. To reduce the possibility of implant loss for the hydrogel Chirila KPro, a number of antiinflammatory drugs that have been used to treat other corneal melting conditions were investigated for their effect on initial collagenase activity after the implantation of KPro material into the rabbit cornea.
METHODSPoly(2-hydroxyethyl methacrylate) sponge pieces were implanted into rabbit corneas. Prednisolone, tetracycline, medroxyprogesterone, acetylcysteine, and sodium citrate were assessed for effects on gelatinolytic activity and stromal collagenase [matrix metalloprotease-1 (MMP-1)] production in vivo and in vitro by using zymography and Western blotting techniques.
RESULTSWhereas all five anticollagenase drugs were effective in reducing gelatinolytic activity in vitro, many were ineffective in vivo. However, medroxyprogesterone caused a reduction of gelatinolytic activity in vivo. The amount of MMP-1, as measured by immunoblotting, also was reduced by medroxyprogesterone treatment when compared with untreated controls. An increase in the apparent molecular weight of MMP-1 in operated corneas appears to be the result of the association of MMP-1 with collagen fragments resulting from the surgical trauma.
CONCLUSIONThis study indicates that topical medroxyprogesterone may be a useful adjunctive therapy after prosthokeratoplasty.</abstract><cop>United States</cop><pub>Lippincott-Raven Publishers</pub><pmid>9436888</pmid><doi>10.1097/00003226-199801000-00016</doi><tpages>1</tpages></addata></record> |
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subjects | Acetylcysteine - administration & dosage Acetylcysteine - pharmacology Administration, Topical Animals Blotting, Western Citrates - administration & dosage Citrates - pharmacology Collagenases - metabolism Cornea - drug effects Cornea - enzymology Cornea - surgery Disease Models, Animal Electrophoresis, Polyacrylamide Gel Gelatinases - metabolism Graft Survival Implants, Experimental Matrix Metalloproteinase Inhibitors Medroxyprogesterone - administration & dosage Medroxyprogesterone - pharmacology Methacrylates Ophthalmic Solutions Prednisolone - administration & dosage Prednisolone - pharmacology Rabbits Tetracycline - administration & dosage Tetracycline - pharmacology Treatment Outcome |
title | Assessment of Anticollagenase Treatments After Insertion of a Keratoprosthetic Material in the Rabbit Cornea |
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