Short-term treatment with metformin reduces hepatic lipid accumulation but induces liver inflammation in obese mice

Detalhes bibliográficos
Autor(a) principal: de Souza Teixeira, Alexandre Abilio
Data de Publicação: 2018
Outros Autores: Souza, Camila O., Biondo, Luana A., Sanches Silveira, Loreana [UNESP], Lima, Edson A., Batatinha, Helena A., Araujo, Adriane Pereira, Alves, Michele Joana, Hirabara, Sandro Massao, Curi, Rui, Neto, José Cesar Rosa
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.1007/s10787-018-0443-7
http://hdl.handle.net/11449/170674
Resumo: The study aimed to evaluate the metabolic and inflammatory effects of short-term treatments (10 days) with metformin (MET) on the NAFLD caused by a high-fat diet (HFD) in C57BL/6 mice. After the treatment, histological liver slices were obtained, hepatocytes and macrophages were extracted and cultured with phosphate buffered saline, LPS (2.5 µg/mL) and MET (1 µM) for 24 h. Cytokine levels were determined by ELISA. NAFLD caused by the HFD was partially reduced by MET. The lipid accumulation induced by the HFD was not associated with liver inflammation; however, MET seemed to promote pro-inflammatory effects in liver, since it increased hepatic concentration of IL-1β, TNF-α, IL-6, MCP-1 and IFN-γ. Similarly, MET increased the concentration of IL-1β, IL-6 in hepatocyte cultures. However, in macrophages culture, MET lowered levels of IL-1β, IL-6 and TNF-α stimulated by LPS. Overall, MET reduced liver NAFLD but promoted hepatocyte increase in pro-inflammatory cytokines, thus, leading to liver inflammation.
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spelling Short-term treatment with metformin reduces hepatic lipid accumulation but induces liver inflammation in obese miceInflammationLiverMetforminObesityThe study aimed to evaluate the metabolic and inflammatory effects of short-term treatments (10 days) with metformin (MET) on the NAFLD caused by a high-fat diet (HFD) in C57BL/6 mice. After the treatment, histological liver slices were obtained, hepatocytes and macrophages were extracted and cultured with phosphate buffered saline, LPS (2.5 µg/mL) and MET (1 µM) for 24 h. Cytokine levels were determined by ELISA. NAFLD caused by the HFD was partially reduced by MET. The lipid accumulation induced by the HFD was not associated with liver inflammation; however, MET seemed to promote pro-inflammatory effects in liver, since it increased hepatic concentration of IL-1β, TNF-α, IL-6, MCP-1 and IFN-γ. Similarly, MET increased the concentration of IL-1β, IL-6 in hepatocyte cultures. However, in macrophages culture, MET lowered levels of IL-1β, IL-6 and TNF-α stimulated by LPS. Overall, MET reduced liver NAFLD but promoted hepatocyte increase in pro-inflammatory cytokines, thus, leading to liver inflammation.Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Immunometabolism Research Group Department of Cell Biology and Development Institute of Biomedical Sciences University of São PauloExercise and Immunometabolism Research Group Department of Physical Education UNESPDepartment of Physiology and Biophysics Institute of Biomedical Sciences University of São PauloCruzeiro do Sul UniversityExercise and Immunometabolism Research Group Department of Physical Education UNESPFAPESP: 2015/16777-0FAPESP: 2016/01409-8Universidade de São Paulo (USP)Universidade Estadual Paulista (Unesp)Cruzeiro do Sul Universityde Souza Teixeira, Alexandre AbilioSouza, Camila O.Biondo, Luana A.Sanches Silveira, Loreana [UNESP]Lima, Edson A.Batatinha, Helena A.Araujo, Adriane PereiraAlves, Michele JoanaHirabara, Sandro MassaoCuri, RuiNeto, José Cesar Rosa2018-12-11T16:51:56Z2018-12-11T16:51:56Z2018-08-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article1103-1115application/pdfhttp://dx.doi.org/10.1007/s10787-018-0443-7Inflammopharmacology, v. 26, n. 4, p. 1103-1115, 2018.1568-56080925-4692http://hdl.handle.net/11449/17067410.1007/s10787-018-0443-72-s2.0-850421368212-s2.0-85042136821.pdfScopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengInflammopharmacology0,9250,925info:eu-repo/semantics/openAccess2023-11-24T06:13:42Zoai:repositorio.unesp.br:11449/170674Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-05T18:35:11.655956Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Short-term treatment with metformin reduces hepatic lipid accumulation but induces liver inflammation in obese mice
title Short-term treatment with metformin reduces hepatic lipid accumulation but induces liver inflammation in obese mice
spellingShingle Short-term treatment with metformin reduces hepatic lipid accumulation but induces liver inflammation in obese mice
de Souza Teixeira, Alexandre Abilio
Inflammation
Liver
Metformin
Obesity
title_short Short-term treatment with metformin reduces hepatic lipid accumulation but induces liver inflammation in obese mice
title_full Short-term treatment with metformin reduces hepatic lipid accumulation but induces liver inflammation in obese mice
title_fullStr Short-term treatment with metformin reduces hepatic lipid accumulation but induces liver inflammation in obese mice
title_full_unstemmed Short-term treatment with metformin reduces hepatic lipid accumulation but induces liver inflammation in obese mice
title_sort Short-term treatment with metformin reduces hepatic lipid accumulation but induces liver inflammation in obese mice
author de Souza Teixeira, Alexandre Abilio
author_facet de Souza Teixeira, Alexandre Abilio
Souza, Camila O.
Biondo, Luana A.
Sanches Silveira, Loreana [UNESP]
Lima, Edson A.
Batatinha, Helena A.
Araujo, Adriane Pereira
Alves, Michele Joana
Hirabara, Sandro Massao
Curi, Rui
Neto, José Cesar Rosa
author_role author
author2 Souza, Camila O.
Biondo, Luana A.
Sanches Silveira, Loreana [UNESP]
Lima, Edson A.
Batatinha, Helena A.
Araujo, Adriane Pereira
Alves, Michele Joana
Hirabara, Sandro Massao
Curi, Rui
Neto, José Cesar Rosa
author2_role author
author
author
author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade de São Paulo (USP)
Universidade Estadual Paulista (Unesp)
Cruzeiro do Sul University
dc.contributor.author.fl_str_mv de Souza Teixeira, Alexandre Abilio
Souza, Camila O.
Biondo, Luana A.
Sanches Silveira, Loreana [UNESP]
Lima, Edson A.
Batatinha, Helena A.
Araujo, Adriane Pereira
Alves, Michele Joana
Hirabara, Sandro Massao
Curi, Rui
Neto, José Cesar Rosa
dc.subject.por.fl_str_mv Inflammation
Liver
Metformin
Obesity
topic Inflammation
Liver
Metformin
Obesity
description The study aimed to evaluate the metabolic and inflammatory effects of short-term treatments (10 days) with metformin (MET) on the NAFLD caused by a high-fat diet (HFD) in C57BL/6 mice. After the treatment, histological liver slices were obtained, hepatocytes and macrophages were extracted and cultured with phosphate buffered saline, LPS (2.5 µg/mL) and MET (1 µM) for 24 h. Cytokine levels were determined by ELISA. NAFLD caused by the HFD was partially reduced by MET. The lipid accumulation induced by the HFD was not associated with liver inflammation; however, MET seemed to promote pro-inflammatory effects in liver, since it increased hepatic concentration of IL-1β, TNF-α, IL-6, MCP-1 and IFN-γ. Similarly, MET increased the concentration of IL-1β, IL-6 in hepatocyte cultures. However, in macrophages culture, MET lowered levels of IL-1β, IL-6 and TNF-α stimulated by LPS. Overall, MET reduced liver NAFLD but promoted hepatocyte increase in pro-inflammatory cytokines, thus, leading to liver inflammation.
publishDate 2018
dc.date.none.fl_str_mv 2018-12-11T16:51:56Z
2018-12-11T16:51:56Z
2018-08-01
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://dx.doi.org/10.1007/s10787-018-0443-7
Inflammopharmacology, v. 26, n. 4, p. 1103-1115, 2018.
1568-5608
0925-4692
http://hdl.handle.net/11449/170674
10.1007/s10787-018-0443-7
2-s2.0-85042136821
2-s2.0-85042136821.pdf
url http://dx.doi.org/10.1007/s10787-018-0443-7
http://hdl.handle.net/11449/170674
identifier_str_mv Inflammopharmacology, v. 26, n. 4, p. 1103-1115, 2018.
1568-5608
0925-4692
10.1007/s10787-018-0443-7
2-s2.0-85042136821
2-s2.0-85042136821.pdf
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Inflammopharmacology
0,925
0,925
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 1103-1115
application/pdf
dc.source.none.fl_str_mv Scopus
reponame:Repositório Institucional da UNESP
instname:Universidade Estadual Paulista (UNESP)
instacron:UNESP
instname_str Universidade Estadual Paulista (UNESP)
instacron_str UNESP
institution UNESP
reponame_str Repositório Institucional da UNESP
collection Repositório Institucional da UNESP
repository.name.fl_str_mv Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)
repository.mail.fl_str_mv
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