Evaluation of programmed cell death processes on the lens epithelium of older dogs with diabetic and hypermature cataracts
Autor(a) principal: | |
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Data de Publicação: | 2018 |
Outros Autores: | , , , , , , |
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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Brazilian Journal of Veterinary Research and Animal Science |
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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 |
_version_ |
1797051567258468352 |