Avaliação de bolha fistulante antiglaucomatosa em olhos de coelhos após administração de Bevacizumabe, Acetato de Triancinolona e Mitomicina-C

Detalhes bibliográficos
Autor(a) principal: Hayana Marques do Aragão Rangel
Data de Publicação: 2017
Tipo de documento: Tese
Idioma: por
Título da fonte: Repositório Institucional da UFMG
Texto Completo: http://hdl.handle.net/1843/BUOS-B4WJC2
Resumo: PURPOSE: To investigate the individual and synergistic mechanism of action of bevacizumab, mitomycin C (MMC), and triamcinolone acetonide (TA) during postoperative healing after glaucoma filtration surgery (GFS) in rabbits. METHODS: Both eyes of 45 rabbits of New Zealand breed were subjected to GFS. The rabbits received different treatments during the surgery, including saline solution, MMC, TA, TA + MMC, bevacizumab, and bevacizumab + MMC. MMC and saline solution were used below the conjunctival flap. TA and bevacizumab were used immediately after surgery as subconjunctival injections. The rabbits were evaluated on different days postoperatively. Intraocular pressure (IOP) was measured, and analysis of the bleb was done based on the Moorfields Grading System. The animals were sacrificed on postoperative days (PD) 3, 14, and 30. Histological and immunohistochemical examinations were conducted to assess healing. RESULTS: The bevacizumab + MMC group displayed the lowest IOP at the end of the study (7.7 ± 0.8 mm Hg), followed by MMC (8.8 ± 1.85 mm Hg) and AT + MMC (8.9 ± 0.9 mm Hg) (P = 0.001). The bevacizumab + MMC group displayed the best clinical results in relation to maximum height, central area, and maximum area of the bleb (P < 0.05). The TA + MMC group displayed higher blebs than the MMC group (P < 0.05). Analysis of vascularization of the central and maximum areas of the bleb revealed smaller values in the groups that used MMC on PD 14 and PD 30. During assessment of inflammatory infiltrates, the bevacizumab + MMC group had lower indexes in the whole study, followed by the TA + MMC and MMC groups (P = 0.001). Initially, vascular proliferation was lower in the TA + MMC group. In the intermediary stage, it was lower in the bevacizumab + MMC group. At the end of this study, the MMC group had the lowest indexes (P = 0.001). CONCLUSIONS: The combination of bevacizumab and MMC was effective and safe as a GFS healing modulator in this animal model. The combination of triamcinolone and MMC was also effective, but not so effective as bevacizumab + MMC. The isolated alternative modulators were not as effective as MMC monotherapy.
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spelling Avaliação de bolha fistulante antiglaucomatosa em olhos de coelhos após administração de Bevacizumabe, Acetato de Triancinolona e Mitomicina-CGlaucomaCicatrizaçãoTrabeculectomia ExperimentalAntimitóticosGlaucomaTriancinolona acetonida/uso terapêuticoTrabeculectomiaCicatrizaçãoBevacizumab/uso terapêuticoMedicinaAntimitóticosPURPOSE: To investigate the individual and synergistic mechanism of action of bevacizumab, mitomycin C (MMC), and triamcinolone acetonide (TA) during postoperative healing after glaucoma filtration surgery (GFS) in rabbits. METHODS: Both eyes of 45 rabbits of New Zealand breed were subjected to GFS. The rabbits received different treatments during the surgery, including saline solution, MMC, TA, TA + MMC, bevacizumab, and bevacizumab + MMC. MMC and saline solution were used below the conjunctival flap. TA and bevacizumab were used immediately after surgery as subconjunctival injections. The rabbits were evaluated on different days postoperatively. Intraocular pressure (IOP) was measured, and analysis of the bleb was done based on the Moorfields Grading System. The animals were sacrificed on postoperative days (PD) 3, 14, and 30. Histological and immunohistochemical examinations were conducted to assess healing. RESULTS: The bevacizumab + MMC group displayed the lowest IOP at the end of the study (7.7 ± 0.8 mm Hg), followed by MMC (8.8 ± 1.85 mm Hg) and AT + MMC (8.9 ± 0.9 mm Hg) (P = 0.001). The bevacizumab + MMC group displayed the best clinical results in relation to maximum height, central area, and maximum area of the bleb (P < 0.05). The TA + MMC group displayed higher blebs than the MMC group (P < 0.05). Analysis of vascularization of the central and maximum areas of the bleb revealed smaller values in the groups that used MMC on PD 14 and PD 30. During assessment of inflammatory infiltrates, the bevacizumab + MMC group had lower indexes in the whole study, followed by the TA + MMC and MMC groups (P = 0.001). Initially, vascular proliferation was lower in the TA + MMC group. In the intermediary stage, it was lower in the bevacizumab + MMC group. At the end of this study, the MMC group had the lowest indexes (P = 0.001). CONCLUSIONS: The combination of bevacizumab and MMC was effective and safe as a GFS healing modulator in this animal model. The combination of triamcinolone and MMC was also effective, but not so effective as bevacizumab + MMC. The isolated alternative modulators were not as effective as MMC monotherapy.OBJETIVOS: Investigar a ação do uso de Bevacizumabe, Mitomicina C (MMC) e Acetato de Triancinolona (AT) (isolados e em associação) na cicatrização pós-operatória após trabeculectomia (TREC) em coelhos. MÉTODOS: Quarenta e cinco coelhos albinos da raça Nova Zelândia foram submetidos à TREC em ambos os olhos e receberam, no transoperatório, tratamentos diferentes: solução salina; MMC; AT; AT+MMC; Bevacizumabe; Bevacizumabe+MMC. A MMC e a solução salina foram utilizadas abaixo do retalho conjuntival; AT e Bevacizumabe foram utilizados imediatamente após a cirurgia em injeção subconjuntival. Os coelhos foram avaliados em dias diferentes durante o pós-operatório; mediu-se a pressão intraocular (Po) e fez-se a análise da bolha baseada no sistema de classificação de bolha de Moorfields. Os animais foram mortos nos dias 3, 14 e 30 de pós-operatório (DPO). Histologia e imunohistoquímica foram realizadas para avaliar a cicatrização. RESULTADOS: O grupo Bevacizumabe+MMC apresentou menor Po ao final do estudo (7,7 ± 0,8 mmHg), seguido pelos grupos MMC (8,8 ± 1,85 mmHg) e AT+MMC (8,9 ± 0,9 mmHg) (p=0,001). O grupo Bevacizumabe+MMC apresentou melhores resultados clínicos em relação à altura máxima da bolha, à área central da bolha e à área máxima da bolha (p<0,05); o grupo AT+MMC apresentou bolhas mais altas que o grupo MMC (p<0,05). A análise de vascularização da área central e da área máxima da bolha mostrou resultados menores nos grupos que utilizaram MMC em 14DPO e 30DPO. Na avaliação do infiltrado inflamatório, o grupo Bevacizumabe+MMC apresentou menores índices em todo o estudo, seguido pelos grupos AT+MMC e MMC (p=0,001). A proliferação vascular inicialmente foi menor no grupo AT+MMC; na fase intermediária, foi menor no grupo Bevacizumabe+MMC; e ao final do estudo, o grupo com menores índices nesse critério foi o MMC (p=0,001). CONCLUSÕES: A associação Bevacizumabe à MMC é efetiva e segura como modulador da cicatrização da TREC neste modelo animal; como também a associação Acetato de Triancinolona a MMC, mas com efeito menor. Os moduladores alternativos isolados não foram tão eficazes como a MMC em monoterapia.Universidade Federal de Minas GeraisUFMGLuciana Bastos RodriguesIvana Duval de AraujoGalton Carvalho VasconcelosJoel Edmur BoteonHévila Tamar Rolim LimaIvana Duval de AraujoHayana Marques do Aragão Rangel2019-08-12T15:04:33Z2019-08-12T15:04:33Z2017-07-17info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/doctoralThesisapplication/pdfhttp://hdl.handle.net/1843/BUOS-B4WJC2info:eu-repo/semantics/openAccessporreponame:Repositório Institucional da UFMGinstname:Universidade Federal de Minas Gerais (UFMG)instacron:UFMG2019-11-14T21:21:11Zoai:repositorio.ufmg.br:1843/BUOS-B4WJC2Repositório InstitucionalPUBhttps://repositorio.ufmg.br/oairepositorio@ufmg.bropendoar:2019-11-14T21:21:11Repositório Institucional da UFMG - Universidade Federal de Minas Gerais (UFMG)false
dc.title.none.fl_str_mv Avaliação de bolha fistulante antiglaucomatosa em olhos de coelhos após administração de Bevacizumabe, Acetato de Triancinolona e Mitomicina-C
title Avaliação de bolha fistulante antiglaucomatosa em olhos de coelhos após administração de Bevacizumabe, Acetato de Triancinolona e Mitomicina-C
spellingShingle Avaliação de bolha fistulante antiglaucomatosa em olhos de coelhos após administração de Bevacizumabe, Acetato de Triancinolona e Mitomicina-C
Hayana Marques do Aragão Rangel
Glaucoma
Cicatrização
Trabeculectomia Experimental
Antimitóticos
Glaucoma
Triancinolona acetonida/uso terapêutico
Trabeculectomia
Cicatrização
Bevacizumab/uso terapêutico
Medicina
Antimitóticos
title_short Avaliação de bolha fistulante antiglaucomatosa em olhos de coelhos após administração de Bevacizumabe, Acetato de Triancinolona e Mitomicina-C
title_full Avaliação de bolha fistulante antiglaucomatosa em olhos de coelhos após administração de Bevacizumabe, Acetato de Triancinolona e Mitomicina-C
title_fullStr Avaliação de bolha fistulante antiglaucomatosa em olhos de coelhos após administração de Bevacizumabe, Acetato de Triancinolona e Mitomicina-C
title_full_unstemmed Avaliação de bolha fistulante antiglaucomatosa em olhos de coelhos após administração de Bevacizumabe, Acetato de Triancinolona e Mitomicina-C
title_sort Avaliação de bolha fistulante antiglaucomatosa em olhos de coelhos após administração de Bevacizumabe, Acetato de Triancinolona e Mitomicina-C
author Hayana Marques do Aragão Rangel
author_facet Hayana Marques do Aragão Rangel
author_role author
dc.contributor.none.fl_str_mv Luciana Bastos Rodrigues
Ivana Duval de Araujo
Galton Carvalho Vasconcelos
Joel Edmur Boteon
Hévila Tamar Rolim Lima
Ivana Duval de Araujo
dc.contributor.author.fl_str_mv Hayana Marques do Aragão Rangel
dc.subject.por.fl_str_mv Glaucoma
Cicatrização
Trabeculectomia Experimental
Antimitóticos
Glaucoma
Triancinolona acetonida/uso terapêutico
Trabeculectomia
Cicatrização
Bevacizumab/uso terapêutico
Medicina
Antimitóticos
topic Glaucoma
Cicatrização
Trabeculectomia Experimental
Antimitóticos
Glaucoma
Triancinolona acetonida/uso terapêutico
Trabeculectomia
Cicatrização
Bevacizumab/uso terapêutico
Medicina
Antimitóticos
description PURPOSE: To investigate the individual and synergistic mechanism of action of bevacizumab, mitomycin C (MMC), and triamcinolone acetonide (TA) during postoperative healing after glaucoma filtration surgery (GFS) in rabbits. METHODS: Both eyes of 45 rabbits of New Zealand breed were subjected to GFS. The rabbits received different treatments during the surgery, including saline solution, MMC, TA, TA + MMC, bevacizumab, and bevacizumab + MMC. MMC and saline solution were used below the conjunctival flap. TA and bevacizumab were used immediately after surgery as subconjunctival injections. The rabbits were evaluated on different days postoperatively. Intraocular pressure (IOP) was measured, and analysis of the bleb was done based on the Moorfields Grading System. The animals were sacrificed on postoperative days (PD) 3, 14, and 30. Histological and immunohistochemical examinations were conducted to assess healing. RESULTS: The bevacizumab + MMC group displayed the lowest IOP at the end of the study (7.7 ± 0.8 mm Hg), followed by MMC (8.8 ± 1.85 mm Hg) and AT + MMC (8.9 ± 0.9 mm Hg) (P = 0.001). The bevacizumab + MMC group displayed the best clinical results in relation to maximum height, central area, and maximum area of the bleb (P < 0.05). The TA + MMC group displayed higher blebs than the MMC group (P < 0.05). Analysis of vascularization of the central and maximum areas of the bleb revealed smaller values in the groups that used MMC on PD 14 and PD 30. During assessment of inflammatory infiltrates, the bevacizumab + MMC group had lower indexes in the whole study, followed by the TA + MMC and MMC groups (P = 0.001). Initially, vascular proliferation was lower in the TA + MMC group. In the intermediary stage, it was lower in the bevacizumab + MMC group. At the end of this study, the MMC group had the lowest indexes (P = 0.001). CONCLUSIONS: The combination of bevacizumab and MMC was effective and safe as a GFS healing modulator in this animal model. The combination of triamcinolone and MMC was also effective, but not so effective as bevacizumab + MMC. The isolated alternative modulators were not as effective as MMC monotherapy.
publishDate 2017
dc.date.none.fl_str_mv 2017-07-17
2019-08-12T15:04:33Z
2019-08-12T15:04:33Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/doctoralThesis
format doctoralThesis
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://hdl.handle.net/1843/BUOS-B4WJC2
url http://hdl.handle.net/1843/BUOS-B4WJC2
dc.language.iso.fl_str_mv por
language por
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Universidade Federal de Minas Gerais
UFMG
publisher.none.fl_str_mv Universidade Federal de Minas Gerais
UFMG
dc.source.none.fl_str_mv reponame:Repositório Institucional da UFMG
instname:Universidade Federal de Minas Gerais (UFMG)
instacron:UFMG
instname_str Universidade Federal de Minas Gerais (UFMG)
instacron_str UFMG
institution UFMG
reponame_str Repositório Institucional da UFMG
collection Repositório Institucional da UFMG
repository.name.fl_str_mv Repositório Institucional da UFMG - Universidade Federal de Minas Gerais (UFMG)
repository.mail.fl_str_mv repositorio@ufmg.br
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