Experimental model of hepatic steatosis by fructose in adult zebrafish: A pilot study
Autor(a) principal: | |
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Data de Publicação: | 2018 |
Outros Autores: | , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Clinical and Biomedical Research |
Texto Completo: | https://seer.ufrgs.br/index.php/hcpa/article/view/77997 |
Resumo: | Introduction: The consumption of fructose has been questioned, since its increase has led to an associated increase in steatosis caused by nonalcoholic fatty liver disease. Despite the advantages presented by the zebrafish as an animal model, at present there are no models of steatosis by fructose in adult zebrafish. The aim of this study is to establish a model of hepatic steatosis by fructose in adult zebrafish.Methods: Firstly, adult zebrafish were daily exposed to 4% or 6% fructose. Then, animals were exposed to 6% fructose every 2 days. The hepatic lipid accumulation was analyzed by Nile Red and Oil Red O staining.Results: The daily exposure to 6% fructose showed increased accumulation of hepatic lipids when compared to 4% and control groups, but the same concentration showed no difference when the exposure happened every 2 days.Conclusion: We can suggest the daily exposure to a concentration of 6% fructose can be considered as a new experimental model of adult zebrafish.Keywords: Fatty liver; fructose; zebrafish |
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Clinical and Biomedical Research |
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Experimental model of hepatic steatosis by fructose in adult zebrafish: A pilot studyFatty liverfructosezebrafishIntroduction: The consumption of fructose has been questioned, since its increase has led to an associated increase in steatosis caused by nonalcoholic fatty liver disease. Despite the advantages presented by the zebrafish as an animal model, at present there are no models of steatosis by fructose in adult zebrafish. The aim of this study is to establish a model of hepatic steatosis by fructose in adult zebrafish.Methods: Firstly, adult zebrafish were daily exposed to 4% or 6% fructose. Then, animals were exposed to 6% fructose every 2 days. The hepatic lipid accumulation was analyzed by Nile Red and Oil Red O staining.Results: The daily exposure to 6% fructose showed increased accumulation of hepatic lipids when compared to 4% and control groups, but the same concentration showed no difference when the exposure happened every 2 days.Conclusion: We can suggest the daily exposure to a concentration of 6% fructose can be considered as a new experimental model of adult zebrafish.Keywords: Fatty liver; fructose; zebrafishHCPA/FAMED/UFRGS2018-07-19info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionPeer-reviewed Articleapplication/pdfhttps://seer.ufrgs.br/index.php/hcpa/article/view/77997Clinical & Biomedical Research; Vol. 38 No. 2 (2018): Clinical and Biomedical ResearchClinical and Biomedical Research; v. 38 n. 2 (2018): Clinical and Biomedical Research2357-9730reponame:Clinical and Biomedical Researchinstname:Universidade Federal do Rio Grande do Sul (UFRGS)instacron:UFRGSenghttps://seer.ufrgs.br/index.php/hcpa/article/view/77997/pdfCopyright (c) 2018 Jéssica Tonin Ferrari, Raquel Ayres, Themis Reverbel da Silveira, Carolina Uribe-Cruzinfo:eu-repo/semantics/openAccessTonin Ferrari, JéssicaAyres, RaquelOrtiz Hammes, ThaisReverbel da Silveira, ThemisUribe-Cruz, Carolina2024-01-19T14:23:02Zoai:seer.ufrgs.br:article/77997Revistahttps://www.seer.ufrgs.br/index.php/hcpaPUBhttps://seer.ufrgs.br/index.php/hcpa/oai||cbr@hcpa.edu.br2357-97302357-9730opendoar:2024-01-19T14:23:02Clinical and Biomedical Research - Universidade Federal do Rio Grande do Sul (UFRGS)false |
dc.title.none.fl_str_mv |
Experimental model of hepatic steatosis by fructose in adult zebrafish: A pilot study |
title |
Experimental model of hepatic steatosis by fructose in adult zebrafish: A pilot study |
spellingShingle |
Experimental model of hepatic steatosis by fructose in adult zebrafish: A pilot study Tonin Ferrari, Jéssica Fatty liver fructose zebrafish |
title_short |
Experimental model of hepatic steatosis by fructose in adult zebrafish: A pilot study |
title_full |
Experimental model of hepatic steatosis by fructose in adult zebrafish: A pilot study |
title_fullStr |
Experimental model of hepatic steatosis by fructose in adult zebrafish: A pilot study |
title_full_unstemmed |
Experimental model of hepatic steatosis by fructose in adult zebrafish: A pilot study |
title_sort |
Experimental model of hepatic steatosis by fructose in adult zebrafish: A pilot study |
author |
Tonin Ferrari, Jéssica |
author_facet |
Tonin Ferrari, Jéssica Ayres, Raquel Ortiz Hammes, Thais Reverbel da Silveira, Themis Uribe-Cruz, Carolina |
author_role |
author |
author2 |
Ayres, Raquel Ortiz Hammes, Thais Reverbel da Silveira, Themis Uribe-Cruz, Carolina |
author2_role |
author author author author |
dc.contributor.author.fl_str_mv |
Tonin Ferrari, Jéssica Ayres, Raquel Ortiz Hammes, Thais Reverbel da Silveira, Themis Uribe-Cruz, Carolina |
dc.subject.por.fl_str_mv |
Fatty liver fructose zebrafish |
topic |
Fatty liver fructose zebrafish |
description |
Introduction: The consumption of fructose has been questioned, since its increase has led to an associated increase in steatosis caused by nonalcoholic fatty liver disease. Despite the advantages presented by the zebrafish as an animal model, at present there are no models of steatosis by fructose in adult zebrafish. The aim of this study is to establish a model of hepatic steatosis by fructose in adult zebrafish.Methods: Firstly, adult zebrafish were daily exposed to 4% or 6% fructose. Then, animals were exposed to 6% fructose every 2 days. The hepatic lipid accumulation was analyzed by Nile Red and Oil Red O staining.Results: The daily exposure to 6% fructose showed increased accumulation of hepatic lipids when compared to 4% and control groups, but the same concentration showed no difference when the exposure happened every 2 days.Conclusion: We can suggest the daily exposure to a concentration of 6% fructose can be considered as a new experimental model of adult zebrafish.Keywords: Fatty liver; fructose; zebrafish |
publishDate |
2018 |
dc.date.none.fl_str_mv |
2018-07-19 |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion Peer-reviewed Article |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
https://seer.ufrgs.br/index.php/hcpa/article/view/77997 |
url |
https://seer.ufrgs.br/index.php/hcpa/article/view/77997 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
https://seer.ufrgs.br/index.php/hcpa/article/view/77997/pdf |
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 |
HCPA/FAMED/UFRGS |
publisher.none.fl_str_mv |
HCPA/FAMED/UFRGS |
dc.source.none.fl_str_mv |
Clinical & Biomedical Research; Vol. 38 No. 2 (2018): Clinical and Biomedical Research Clinical and Biomedical Research; v. 38 n. 2 (2018): Clinical and Biomedical Research 2357-9730 reponame:Clinical and Biomedical Research instname:Universidade Federal do Rio Grande do Sul (UFRGS) instacron:UFRGS |
instname_str |
Universidade Federal do Rio Grande do Sul (UFRGS) |
instacron_str |
UFRGS |
institution |
UFRGS |
reponame_str |
Clinical and Biomedical Research |
collection |
Clinical and Biomedical Research |
repository.name.fl_str_mv |
Clinical and Biomedical Research - Universidade Federal do Rio Grande do Sul (UFRGS) |
repository.mail.fl_str_mv |
||cbr@hcpa.edu.br |
_version_ |
1799767054580973568 |