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
Hauptverfasser: Fitton, J Helen, Ziegelaar, Brian W, Hicks, Celia R, Clayton, Anthony B, Crawford, Geoffrey J, Constable, Ian J, Chirila, Traian V
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container_end_page 108
container_issue 1
container_start_page 108
container_title Cornea
container_volume 17
creator Fitton, J Helen
Ziegelaar, Brian W
Hicks, Celia R
Clayton, Anthony B
Crawford, Geoffrey J
Constable, Ian J
Chirila, Traian V
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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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. 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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. 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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 &amp; dosage</topic><topic>Acetylcysteine - pharmacology</topic><topic>Administration, Topical</topic><topic>Animals</topic><topic>Blotting, Western</topic><topic>Citrates - administration &amp; 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 &amp; 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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. 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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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