Regulation of hepatic TRB3/Akt interaction induced by physical exercise and its effect on the hepatic glucose production in an insulin resistance state

Detalhes bibliográficos
Autor(a) principal: Marinho, Rodolfo [UNESP]
Data de Publicação: 2015
Outros Autores: Mekary, Rania A., Muñoz, Vitor Rosetto, Gomes, Ricardo José, Pauli, José Rodrigo [UNESP], Moura, Leandro Pereira de [UNESP]
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.1186/s13098-015-0064-x
http://hdl.handle.net/11449/131460
Resumo: To maintain euglycemia in healthy organisms, hepatic glucose production is increased during fasting and decreased during the postprandial period. This whole process is supported by insulin levels. These responses are associated with the insulin signaling pathway and the reduction in the activity of key gluconeogenic enzymes, resulting in a decrease of hepatic glucose production. On the other hand, defects in the liver insulin signaling pathway might promote inadequate suppression of gluconeogenesis, leading to hyperglycemia during fasting and after meals. The hepatocyte nuclear factor 4, the transcription cofactor PGC1-α, and the transcription factor Foxo1 have fundamental roles in regulating gluconeogenesis. The loss of insulin action is associated with the production of pro-inflammatory biomolecules in obesity conditions. Among the molecular mechanisms involved, we emphasize in this review the participation of TRB3 protein (a mammalian homolog of Drosophila tribbles), which is able to inhibit Akt activity and, thereby, maintain Foxo1 activity in the nucleus of hepatocytes, inducing hyperglycemia. In contrast, physical exercise has been shown as an important tool to reduce insulin resistance in the liver by reducing the inflammatory process, including the inhibition of TRB3 and, therefore, suppressing gluconeogenesis. The understanding of these new mechanisms by which physical exercise regulates glucose homeostasis has critical importance for the understanding and prevention of diabetes.
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spelling Regulation of hepatic TRB3/Akt interaction induced by physical exercise and its effect on the hepatic glucose production in an insulin resistance stateHepatic glucose productionInsulin resistanceLiverPhysical exerciseTrb3To maintain euglycemia in healthy organisms, hepatic glucose production is increased during fasting and decreased during the postprandial period. This whole process is supported by insulin levels. These responses are associated with the insulin signaling pathway and the reduction in the activity of key gluconeogenic enzymes, resulting in a decrease of hepatic glucose production. On the other hand, defects in the liver insulin signaling pathway might promote inadequate suppression of gluconeogenesis, leading to hyperglycemia during fasting and after meals. The hepatocyte nuclear factor 4, the transcription cofactor PGC1-α, and the transcription factor Foxo1 have fundamental roles in regulating gluconeogenesis. The loss of insulin action is associated with the production of pro-inflammatory biomolecules in obesity conditions. Among the molecular mechanisms involved, we emphasize in this review the participation of TRB3 protein (a mammalian homolog of Drosophila tribbles), which is able to inhibit Akt activity and, thereby, maintain Foxo1 activity in the nucleus of hepatocytes, inducing hyperglycemia. In contrast, physical exercise has been shown as an important tool to reduce insulin resistance in the liver by reducing the inflammatory process, including the inhibition of TRB3 and, therefore, suppressing gluconeogenesis. The understanding of these new mechanisms by which physical exercise regulates glucose homeostasis has critical importance for the understanding and prevention of diabetes.São Paulo State University, UNESP, Rio Claro, SP Brazil ; Faculty of Applied Science, University of Campinas (UNICAMP), Rua Pedro Zaccaria, 1300, Jardim Santa Luzia, Limeira, SP Brazil.Department of Social and Administrative Sciences, MCPHS University, Boston, MA USA ; Department of Nutrition, Harvard T. Chan School of Public Health, Boston, MA USA.Faculty of Applied Science, University of Campinas (UNICAMP), Rua Pedro Zaccaria, 1300, Jardim Santa Luzia, Limeira, SP Brazil.Department of Biosciences, São Paulo Federal University (UNIFESP), Santos, SP Brazil.São Paulo State University, UNESP, Rio Claro, SP Brazil ; Faculty of Applied Science, University of Campinas (UNICAMP), Rua Pedro Zaccaria, 1300, Jardim Santa Luzia, Limeira, SP Brazil.Universidade Estadual Paulista (Unesp)Department of Social and Administrative Sciences, MCPHS University, Boston, MA USA ; Department of Nutrition, Harvard T. Chan School of Public Health, Boston, MA USA.Universidade Estadual de Campinas (UNICAMP)Universidade Federal de São Paulo (UNIFESP)Marinho, Rodolfo [UNESP]Mekary, Rania A.Muñoz, Vitor RosettoGomes, Ricardo JoséPauli, José Rodrigo [UNESP]Moura, Leandro Pereira de [UNESP]2015-12-07T15:35:53Z2015-12-07T15:35:53Z2015info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article67application/pdfhttp://dx.doi.org/10.1186/s13098-015-0064-xDiabetology & Metabolic Syndrome, v. 7, p. 67, 2015.1758-5996http://hdl.handle.net/11449/13146010.1186/s13098-015-0064-xPMC4539706.pdf26288661PMC4539706PubMedreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengDiabetology & Metabolic Syndrome2.4130,943info:eu-repo/semantics/openAccess2023-12-06T06:19:35Zoai:repositorio.unesp.br:11449/131460Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-05T19:38:22.385172Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Regulation of hepatic TRB3/Akt interaction induced by physical exercise and its effect on the hepatic glucose production in an insulin resistance state
title Regulation of hepatic TRB3/Akt interaction induced by physical exercise and its effect on the hepatic glucose production in an insulin resistance state
spellingShingle Regulation of hepatic TRB3/Akt interaction induced by physical exercise and its effect on the hepatic glucose production in an insulin resistance state
Marinho, Rodolfo [UNESP]
Hepatic glucose production
Insulin resistance
Liver
Physical exercise
Trb3
title_short Regulation of hepatic TRB3/Akt interaction induced by physical exercise and its effect on the hepatic glucose production in an insulin resistance state
title_full Regulation of hepatic TRB3/Akt interaction induced by physical exercise and its effect on the hepatic glucose production in an insulin resistance state
title_fullStr Regulation of hepatic TRB3/Akt interaction induced by physical exercise and its effect on the hepatic glucose production in an insulin resistance state
title_full_unstemmed Regulation of hepatic TRB3/Akt interaction induced by physical exercise and its effect on the hepatic glucose production in an insulin resistance state
title_sort Regulation of hepatic TRB3/Akt interaction induced by physical exercise and its effect on the hepatic glucose production in an insulin resistance state
author Marinho, Rodolfo [UNESP]
author_facet Marinho, Rodolfo [UNESP]
Mekary, Rania A.
Muñoz, Vitor Rosetto
Gomes, Ricardo José
Pauli, José Rodrigo [UNESP]
Moura, Leandro Pereira de [UNESP]
author_role author
author2 Mekary, Rania A.
Muñoz, Vitor Rosetto
Gomes, Ricardo José
Pauli, José Rodrigo [UNESP]
Moura, Leandro Pereira de [UNESP]
author2_role author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade Estadual Paulista (Unesp)
Department of Social and Administrative Sciences, MCPHS University, Boston, MA USA ; Department of Nutrition, Harvard T. Chan School of Public Health, Boston, MA USA.
Universidade Estadual de Campinas (UNICAMP)
Universidade Federal de São Paulo (UNIFESP)
dc.contributor.author.fl_str_mv Marinho, Rodolfo [UNESP]
Mekary, Rania A.
Muñoz, Vitor Rosetto
Gomes, Ricardo José
Pauli, José Rodrigo [UNESP]
Moura, Leandro Pereira de [UNESP]
dc.subject.por.fl_str_mv Hepatic glucose production
Insulin resistance
Liver
Physical exercise
Trb3
topic Hepatic glucose production
Insulin resistance
Liver
Physical exercise
Trb3
description To maintain euglycemia in healthy organisms, hepatic glucose production is increased during fasting and decreased during the postprandial period. This whole process is supported by insulin levels. These responses are associated with the insulin signaling pathway and the reduction in the activity of key gluconeogenic enzymes, resulting in a decrease of hepatic glucose production. On the other hand, defects in the liver insulin signaling pathway might promote inadequate suppression of gluconeogenesis, leading to hyperglycemia during fasting and after meals. The hepatocyte nuclear factor 4, the transcription cofactor PGC1-α, and the transcription factor Foxo1 have fundamental roles in regulating gluconeogenesis. The loss of insulin action is associated with the production of pro-inflammatory biomolecules in obesity conditions. Among the molecular mechanisms involved, we emphasize in this review the participation of TRB3 protein (a mammalian homolog of Drosophila tribbles), which is able to inhibit Akt activity and, thereby, maintain Foxo1 activity in the nucleus of hepatocytes, inducing hyperglycemia. In contrast, physical exercise has been shown as an important tool to reduce insulin resistance in the liver by reducing the inflammatory process, including the inhibition of TRB3 and, therefore, suppressing gluconeogenesis. The understanding of these new mechanisms by which physical exercise regulates glucose homeostasis has critical importance for the understanding and prevention of diabetes.
publishDate 2015
dc.date.none.fl_str_mv 2015-12-07T15:35:53Z
2015-12-07T15:35:53Z
2015
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/10.1186/s13098-015-0064-x
Diabetology & Metabolic Syndrome, v. 7, p. 67, 2015.
1758-5996
http://hdl.handle.net/11449/131460
10.1186/s13098-015-0064-x
PMC4539706.pdf
26288661
PMC4539706
url http://dx.doi.org/10.1186/s13098-015-0064-x
http://hdl.handle.net/11449/131460
identifier_str_mv Diabetology & Metabolic Syndrome, v. 7, p. 67, 2015.
1758-5996
10.1186/s13098-015-0064-x
PMC4539706.pdf
26288661
PMC4539706
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Diabetology & Metabolic Syndrome
2.413
0,943
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 67
application/pdf
dc.source.none.fl_str_mv PubMed
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)
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