Regulation of hepatic TRB3/Akt interaction induced by physical exercise and its effect on the hepatic glucose production in an insulin resistance state
Autor(a) principal: | |
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Data de Publicação: | 2015 |
Outros Autores: | , , , , |
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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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) |
repository.mail.fl_str_mv |
|
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1808129099385798656 |