Evaluation of programmed cell death processes on the lens epithelium of older dogs with diabetic and hypermature cataracts

Detalhes bibliográficos
Autor(a) principal: Hvenegaard, Ana Paula Franco do Amaral
Data de Publicação: 2018
Outros Autores: Barros, Paulo Sergio de Moraes, Safatle, Angélica Mendonça Vaz, Braga-Sá, Michelle Barbosa Pereira, Melo, Luana Vicente, Santana, Ana Carolina, Hossy, Bryan Hudson, Miguel, Nadia Campos de Oliveira
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Brazilian Journal of Veterinary Research and Animal Science
Texto Completo: https://www.revistas.usp.br/bjvras/article/view/133668
Resumo: It is well known that posterior capsule opacification (PCO), one of the most common late postoperative complications of cataract surgery, is mainly caused by proliferation and differentiation of remaining lens epithelial cells (LECs) on the posterior lens capsule. Many authors suggest that alterations induced by the pathophysiology of cataracts, its metabolism and the use of 0.1% trypan blue (TB) must cause some degree of cellular damage on these cells, wicht would help to prevent and/or reduce the incidence of PCO after cataract surgery in humans. Therefore, the aim of this study was to evaluate the expression of cell death markers on LECs of older dogs with diabetic and hypermature cataracts, after capsulorhexis, both using 0.1% TB. Twenty samples collected from 13 dogs of different breeds, with ages varying from 8 to 12 years-old, with diabetic and hypermature cataracts, which had been subjected to phacoemulsification surgery (Phaco) using 0.1% TB for staining were studied. Animals were classified as dogs with diabetic (DC) and hypermature cataracts (HC), and expression of molecular markers for apoptosis and autophagy (caspase-3 and beclin-1) on LECs were obtained by immunofluorescence technique. The expression of caspase-3 and beclin-1 was observed in every studied sample and did not differ between groups. In conclusion, our findings suggest that apoptosis and autophagy processes occur to LECs in older dogs presenting diabetic and hypermature cataracts after Phaco utilizing 0.1% TB. Our results may be helpful to future studies of PCO in post-phacoemulsification surgery patients.
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spelling Evaluation of programmed cell death processes on the lens epithelium of older dogs with diabetic and hypermature cataractsAvaliação dos processos de morte celular programada no epitélio da lente de cães idosos com catarata diabética e hipermaduraCataractsDiabetesApoptosisAutophagyLens epithelium cellsCatarataDiabetesApoptoseAutofagiaEpitélio anterior da lenteIt is well known that posterior capsule opacification (PCO), one of the most common late postoperative complications of cataract surgery, is mainly caused by proliferation and differentiation of remaining lens epithelial cells (LECs) on the posterior lens capsule. Many authors suggest that alterations induced by the pathophysiology of cataracts, its metabolism and the use of 0.1% trypan blue (TB) must cause some degree of cellular damage on these cells, wicht would help to prevent and/or reduce the incidence of PCO after cataract surgery in humans. Therefore, the aim of this study was to evaluate the expression of cell death markers on LECs of older dogs with diabetic and hypermature cataracts, after capsulorhexis, both using 0.1% TB. Twenty samples collected from 13 dogs of different breeds, with ages varying from 8 to 12 years-old, with diabetic and hypermature cataracts, which had been subjected to phacoemulsification surgery (Phaco) using 0.1% TB for staining were studied. Animals were classified as dogs with diabetic (DC) and hypermature cataracts (HC), and expression of molecular markers for apoptosis and autophagy (caspase-3 and beclin-1) on LECs were obtained by immunofluorescence technique. The expression of caspase-3 and beclin-1 was observed in every studied sample and did not differ between groups. In conclusion, our findings suggest that apoptosis and autophagy processes occur to LECs in older dogs presenting diabetic and hypermature cataracts after Phaco utilizing 0.1% TB. Our results may be helpful to future studies of PCO in post-phacoemulsification surgery patients.A opacificação da cápsula posterior da lente do globo ocular é a complicação mais observada após a remoção da lente. Essa patologia é causada principalmente pela proliferação e diferenciação das células do epitélio anterior da lente em sua cápsula posterior. Muitos autores sugerem que alterações induzidas pelo metabolismo e/ou patofisiologia da catarata e o uso do corante de azul de tripan a 0,1% devam causar algum dano a essas células, o que supostamente ajudaria a prevenir e reduzir a incidência de tal complicação em humanos. Este trabalho avaliou a expressão de marcadores de morte celular no epitélio anterior da lente de cães idosos com catarata diabética e hipermadura, após capsulorrexe realizada com o emprego do azul de tripan a 0,1%. Foram estudadas vinte amostras colhidas de treze cães de diferentes raças, com idades variando de oito a doze anos, que apresentavam catarata diabética ou hipermadura e que foram submetidos à facoemulsificação utilizando corante de azul de tripan a 0,1%. Foram designados dois grupos: com catarata diabética (DC) e com catarata hipermadura (HC). A expressão molecular dos marcadores de morte celular por apoptose a autofagia (caspase-3 e beclina-1) no epitélio anterior da lente foi avaliada pela técnica de imunofluorescência. Observou-se que a expressão de caspase-3 e beclina-1 ocorreu em todas as amostras e não foi diferente entre os grupos. Os achados deste estudo sugerem que o processo de morte celular por apoptose e autofagia ocorre no epitélio anterior da lente de cães idosos com catarata diabética e hipermadura submetidos à facoemulsificação com o corante de azul de tripan a 0,1%. Este resultado pode ser útil para estudos futuros da opacidade da cápsula posterior da lente em cães submetidos à facoemulsificação.Universidade de São Paulo. Faculdade de Medicina Veterinária e Zootecnia2018-07-26info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfhttps://www.revistas.usp.br/bjvras/article/view/13366810.11606/issn.1678-4456.bjvras.2018.133668Brazilian Journal of Veterinary Research and Animal Science; Vol. 55 Núm. 2 (2018); e133668Brazilian Journal of Veterinary Research and Animal Science; Vol. 55 No. 2 (2018); e133668Brazilian Journal of Veterinary Research and Animal Science; v. 55 n. 2 (2018); e133668Brazilian Journal of Veterinary Research and Animal Science; V. 55 N. 2 (2018); e1336681678-44561413-9596reponame:Brazilian Journal of Veterinary Research and Animal Scienceinstname:Faculdade de Medicina Veterinária e Zootecnia da Universidade de São Paulo (FMVZ-USP)instacron:USPenghttps://www.revistas.usp.br/bjvras/article/view/133668/141921Copyright (c) 2018 Brazilian Journal of Veterinary Research and Animal Scienceinfo:eu-repo/semantics/openAccessHvenegaard, Ana Paula Franco do AmaralBarros, Paulo Sergio de MoraesSafatle, Angélica Mendonça VazBraga-Sá, Michelle Barbosa PereiraMelo, Luana VicenteSantana, Ana CarolinaHossy, Bryan HudsonMiguel, Nadia Campos de Oliveira2020-06-23T04:03:01Zoai:revistas.usp.br:article/133668Revistahttps://www.revistas.usp.br/bjvrasPUBhttps://www.revistas.usp.br/bjvras/oaibjvras@usp.br1413-95961413-9596opendoar:https://www.revistas.usp.br/bjvras/index2023-01-12T16:44:00.698256Brazilian Journal of Veterinary Research and Animal Science - Faculdade de Medicina Veterinária e Zootecnia da Universidade de São Paulo (FMVZ-USP)false
dc.title.none.fl_str_mv Evaluation of programmed cell death processes on the lens epithelium of older dogs with diabetic and hypermature cataracts
Avaliação dos processos de morte celular programada no epitélio da lente de cães idosos com catarata diabética e hipermadura
title Evaluation of programmed cell death processes on the lens epithelium of older dogs with diabetic and hypermature cataracts
spellingShingle Evaluation of programmed cell death processes on the lens epithelium of older dogs with diabetic and hypermature cataracts
Hvenegaard, Ana Paula Franco do Amaral
Cataracts
Diabetes
Apoptosis
Autophagy
Lens epithelium cells
Catarata
Diabetes
Apoptose
Autofagia
Epitélio anterior da lente
title_short Evaluation of programmed cell death processes on the lens epithelium of older dogs with diabetic and hypermature cataracts
title_full Evaluation of programmed cell death processes on the lens epithelium of older dogs with diabetic and hypermature cataracts
title_fullStr Evaluation of programmed cell death processes on the lens epithelium of older dogs with diabetic and hypermature cataracts
title_full_unstemmed Evaluation of programmed cell death processes on the lens epithelium of older dogs with diabetic and hypermature cataracts
title_sort Evaluation of programmed cell death processes on the lens epithelium of older dogs with diabetic and hypermature cataracts
author Hvenegaard, Ana Paula Franco do Amaral
author_facet Hvenegaard, Ana Paula Franco do Amaral
Barros, Paulo Sergio de Moraes
Safatle, Angélica Mendonça Vaz
Braga-Sá, Michelle Barbosa Pereira
Melo, Luana Vicente
Santana, Ana Carolina
Hossy, Bryan Hudson
Miguel, Nadia Campos de Oliveira
author_role author
author2 Barros, Paulo Sergio de Moraes
Safatle, Angélica Mendonça Vaz
Braga-Sá, Michelle Barbosa Pereira
Melo, Luana Vicente
Santana, Ana Carolina
Hossy, Bryan Hudson
Miguel, Nadia Campos de Oliveira
author2_role author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Hvenegaard, Ana Paula Franco do Amaral
Barros, Paulo Sergio de Moraes
Safatle, Angélica Mendonça Vaz
Braga-Sá, Michelle Barbosa Pereira
Melo, Luana Vicente
Santana, Ana Carolina
Hossy, Bryan Hudson
Miguel, Nadia Campos de Oliveira
dc.subject.por.fl_str_mv Cataracts
Diabetes
Apoptosis
Autophagy
Lens epithelium cells
Catarata
Diabetes
Apoptose
Autofagia
Epitélio anterior da lente
topic Cataracts
Diabetes
Apoptosis
Autophagy
Lens epithelium cells
Catarata
Diabetes
Apoptose
Autofagia
Epitélio anterior da lente
description It is well known that posterior capsule opacification (PCO), one of the most common late postoperative complications of cataract surgery, is mainly caused by proliferation and differentiation of remaining lens epithelial cells (LECs) on the posterior lens capsule. Many authors suggest that alterations induced by the pathophysiology of cataracts, its metabolism and the use of 0.1% trypan blue (TB) must cause some degree of cellular damage on these cells, wicht would help to prevent and/or reduce the incidence of PCO after cataract surgery in humans. Therefore, the aim of this study was to evaluate the expression of cell death markers on LECs of older dogs with diabetic and hypermature cataracts, after capsulorhexis, both using 0.1% TB. Twenty samples collected from 13 dogs of different breeds, with ages varying from 8 to 12 years-old, with diabetic and hypermature cataracts, which had been subjected to phacoemulsification surgery (Phaco) using 0.1% TB for staining were studied. Animals were classified as dogs with diabetic (DC) and hypermature cataracts (HC), and expression of molecular markers for apoptosis and autophagy (caspase-3 and beclin-1) on LECs were obtained by immunofluorescence technique. The expression of caspase-3 and beclin-1 was observed in every studied sample and did not differ between groups. In conclusion, our findings suggest that apoptosis and autophagy processes occur to LECs in older dogs presenting diabetic and hypermature cataracts after Phaco utilizing 0.1% TB. Our results may be helpful to future studies of PCO in post-phacoemulsification surgery patients.
publishDate 2018
dc.date.none.fl_str_mv 2018-07-26
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv https://www.revistas.usp.br/bjvras/article/view/133668
10.11606/issn.1678-4456.bjvras.2018.133668
url https://www.revistas.usp.br/bjvras/article/view/133668
identifier_str_mv 10.11606/issn.1678-4456.bjvras.2018.133668
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv https://www.revistas.usp.br/bjvras/article/view/133668/141921
dc.rights.driver.fl_str_mv Copyright (c) 2018 Brazilian Journal of Veterinary Research and Animal Science
info:eu-repo/semantics/openAccess
rights_invalid_str_mv Copyright (c) 2018 Brazilian Journal of Veterinary Research and Animal Science
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Universidade de São Paulo. Faculdade de Medicina Veterinária e Zootecnia
publisher.none.fl_str_mv Universidade de São Paulo. Faculdade de Medicina Veterinária e Zootecnia
dc.source.none.fl_str_mv Brazilian Journal of Veterinary Research and Animal Science; Vol. 55 Núm. 2 (2018); e133668
Brazilian Journal of Veterinary Research and Animal Science; Vol. 55 No. 2 (2018); e133668
Brazilian Journal of Veterinary Research and Animal Science; v. 55 n. 2 (2018); e133668
Brazilian Journal of Veterinary Research and Animal Science; V. 55 N. 2 (2018); e133668
1678-4456
1413-9596
reponame:Brazilian Journal of Veterinary Research and Animal Science
instname:Faculdade de Medicina Veterinária e Zootecnia da Universidade de São Paulo (FMVZ-USP)
instacron:USP
instname_str Faculdade de Medicina Veterinária e Zootecnia da Universidade de São Paulo (FMVZ-USP)
instacron_str USP
institution USP
reponame_str Brazilian Journal of Veterinary Research and Animal Science
collection Brazilian Journal of Veterinary Research and Animal Science
repository.name.fl_str_mv Brazilian Journal of Veterinary Research and Animal Science - Faculdade de Medicina Veterinária e Zootecnia da Universidade de São Paulo (FMVZ-USP)
repository.mail.fl_str_mv bjvras@usp.br
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