Parkinsonia aculeata (Caesalpineaceae) improves high-fat diet-induced insulin resistance in mice through the enhancement of insulin signaling and mitochondrial biogenesis
Autor(a) principal: | |
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Data de Publicação: | 2016 |
Outros Autores: | , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UNESP |
DOI: | 10.1016/j.jep.2016.02.048 |
Texto Completo: | http://dx.doi.org/10.1016/j.jep.2016.02.048 http://hdl.handle.net/11449/168528 |
Resumo: | Ethnopharmacological relevance The search for natural agents that minimize obesity-associated disorders is receiving special attention. Parkinsonia aculeata L. (Caesalpineaceae) has long been used in Brazil as a hypoglycaemic herbal medicine, without any scientific basis. Aims of the study In this context, we aimed to use molecular and physiological methods to study the effect of a hydroethanolic extract partitioned with ethyl acetate from the aerial parts of Parkinsonia aculeata (HEPa/EtOAc) on insulin resistance in a mouse model of diet-induced obesity (DIO). Material and methods Firstly, C57BL/6J mice were fed either with standard rodent chow diet or a high-fat diet (HFD) for 12 consecutive weeks. Then, the animals were treated with HEPa/EtOAc at two doses (125 and 250 mg/kg/day) or metformin (200 mg/kg/day) for 16 days. At the end of the experiment, body weight, fat pad weight, fasting serum glucose (FSG), insulin (FSI) and leptin were measured. Homeostasis Model Assessment for Insulin Resistance (HOMA-IR) was also calculated. Glucose, insulin and pyruvate tolerance tests were performed. The expression and phosphorylation of IRβtyr, Aktser473, AMPKα and PGC1α in liver, muscle and adipose tissue were determined by Western blot analyses. Results Herein we demonstrate for the first time an improvement in insulin resistance following HEPa/EtOAc administration in obese mice, as shown by increased glucose, insulin and pyruvate tolerance, as well as an improvement in FSG, FSI, HOMA-IR and circulating leptin levels, which together are in part due to enhancement of the insulin signaling pathway in its main target tissues. Surprisingly, the increase in activation of the AMPKα-PGC1-α axis by HEPa/EtOAc was similar to that produced by metformin treatment in the liver and muscle tissues. Conclusion In conclusion, P. aculeata appears to be a source of therapeutic agent against obesity-related complications. |
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Parkinsonia aculeata (Caesalpineaceae) improves high-fat diet-induced insulin resistance in mice through the enhancement of insulin signaling and mitochondrial biogenesisAMPKαHerbal medicineInsulin resistanceMitochondrial biogenesisObesityParkinsonia aculeataEthnopharmacological relevance The search for natural agents that minimize obesity-associated disorders is receiving special attention. Parkinsonia aculeata L. (Caesalpineaceae) has long been used in Brazil as a hypoglycaemic herbal medicine, without any scientific basis. Aims of the study In this context, we aimed to use molecular and physiological methods to study the effect of a hydroethanolic extract partitioned with ethyl acetate from the aerial parts of Parkinsonia aculeata (HEPa/EtOAc) on insulin resistance in a mouse model of diet-induced obesity (DIO). Material and methods Firstly, C57BL/6J mice were fed either with standard rodent chow diet or a high-fat diet (HFD) for 12 consecutive weeks. Then, the animals were treated with HEPa/EtOAc at two doses (125 and 250 mg/kg/day) or metformin (200 mg/kg/day) for 16 days. At the end of the experiment, body weight, fat pad weight, fasting serum glucose (FSG), insulin (FSI) and leptin were measured. Homeostasis Model Assessment for Insulin Resistance (HOMA-IR) was also calculated. Glucose, insulin and pyruvate tolerance tests were performed. The expression and phosphorylation of IRβtyr, Aktser473, AMPKα and PGC1α in liver, muscle and adipose tissue were determined by Western blot analyses. Results Herein we demonstrate for the first time an improvement in insulin resistance following HEPa/EtOAc administration in obese mice, as shown by increased glucose, insulin and pyruvate tolerance, as well as an improvement in FSG, FSI, HOMA-IR and circulating leptin levels, which together are in part due to enhancement of the insulin signaling pathway in its main target tissues. Surprisingly, the increase in activation of the AMPKα-PGC1-α axis by HEPa/EtOAc was similar to that produced by metformin treatment in the liver and muscle tissues. Conclusion In conclusion, P. aculeata appears to be a source of therapeutic agent against obesity-related complications.Department of Physiology and Pharmacology Federal University of PernambucoDepartment of Internal Medicine State University of CampinasDepartment of Physical Education São Paulo State University (UNESP)Department of Physical Education São Paulo State University (UNESP)Universidade Federal de Pernambuco (UFPE)Universidade Estadual de Campinas (UNICAMP)Universidade Estadual Paulista (Unesp)Araújo, Tiago GomesDe Oliveira, Alexandre Gabarra [UNESP]Vecina, Juliana FalcatoMarin, Rodrigo MiguelFranco, Eryvelton SouzaAbdalla Saad, Mario J.De Sousa Maia, Maria Bernadete2018-12-11T16:41:39Z2018-12-11T16:41:39Z2016-05-13info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article95-102application/pdfhttp://dx.doi.org/10.1016/j.jep.2016.02.048Journal of Ethnopharmacology, v. 183, p. 95-102.1872-75730378-8741http://hdl.handle.net/11449/16852810.1016/j.jep.2016.02.0482-s2.0-849623093922-s2.0-84962309392.pdfScopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengJournal of Ethnopharmacology1,150info:eu-repo/semantics/openAccess2024-01-17T06:29:35Zoai:repositorio.unesp.br:11449/168528Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-05T23:18:14.651430Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false |
dc.title.none.fl_str_mv |
Parkinsonia aculeata (Caesalpineaceae) improves high-fat diet-induced insulin resistance in mice through the enhancement of insulin signaling and mitochondrial biogenesis |
title |
Parkinsonia aculeata (Caesalpineaceae) improves high-fat diet-induced insulin resistance in mice through the enhancement of insulin signaling and mitochondrial biogenesis |
spellingShingle |
Parkinsonia aculeata (Caesalpineaceae) improves high-fat diet-induced insulin resistance in mice through the enhancement of insulin signaling and mitochondrial biogenesis Parkinsonia aculeata (Caesalpineaceae) improves high-fat diet-induced insulin resistance in mice through the enhancement of insulin signaling and mitochondrial biogenesis Araújo, Tiago Gomes AMPKα Herbal medicine Insulin resistance Mitochondrial biogenesis Obesity Parkinsonia aculeata Araújo, Tiago Gomes AMPKα Herbal medicine Insulin resistance Mitochondrial biogenesis Obesity Parkinsonia aculeata |
title_short |
Parkinsonia aculeata (Caesalpineaceae) improves high-fat diet-induced insulin resistance in mice through the enhancement of insulin signaling and mitochondrial biogenesis |
title_full |
Parkinsonia aculeata (Caesalpineaceae) improves high-fat diet-induced insulin resistance in mice through the enhancement of insulin signaling and mitochondrial biogenesis |
title_fullStr |
Parkinsonia aculeata (Caesalpineaceae) improves high-fat diet-induced insulin resistance in mice through the enhancement of insulin signaling and mitochondrial biogenesis Parkinsonia aculeata (Caesalpineaceae) improves high-fat diet-induced insulin resistance in mice through the enhancement of insulin signaling and mitochondrial biogenesis |
title_full_unstemmed |
Parkinsonia aculeata (Caesalpineaceae) improves high-fat diet-induced insulin resistance in mice through the enhancement of insulin signaling and mitochondrial biogenesis Parkinsonia aculeata (Caesalpineaceae) improves high-fat diet-induced insulin resistance in mice through the enhancement of insulin signaling and mitochondrial biogenesis |
title_sort |
Parkinsonia aculeata (Caesalpineaceae) improves high-fat diet-induced insulin resistance in mice through the enhancement of insulin signaling and mitochondrial biogenesis |
author |
Araújo, Tiago Gomes |
author_facet |
Araújo, Tiago Gomes Araújo, Tiago Gomes De Oliveira, Alexandre Gabarra [UNESP] Vecina, Juliana Falcato Marin, Rodrigo Miguel Franco, Eryvelton Souza Abdalla Saad, Mario J. De Sousa Maia, Maria Bernadete De Oliveira, Alexandre Gabarra [UNESP] Vecina, Juliana Falcato Marin, Rodrigo Miguel Franco, Eryvelton Souza Abdalla Saad, Mario J. De Sousa Maia, Maria Bernadete |
author_role |
author |
author2 |
De Oliveira, Alexandre Gabarra [UNESP] Vecina, Juliana Falcato Marin, Rodrigo Miguel Franco, Eryvelton Souza Abdalla Saad, Mario J. De Sousa Maia, Maria Bernadete |
author2_role |
author author author author author author |
dc.contributor.none.fl_str_mv |
Universidade Federal de Pernambuco (UFPE) Universidade Estadual de Campinas (UNICAMP) Universidade Estadual Paulista (Unesp) |
dc.contributor.author.fl_str_mv |
Araújo, Tiago Gomes De Oliveira, Alexandre Gabarra [UNESP] Vecina, Juliana Falcato Marin, Rodrigo Miguel Franco, Eryvelton Souza Abdalla Saad, Mario J. De Sousa Maia, Maria Bernadete |
dc.subject.por.fl_str_mv |
AMPKα Herbal medicine Insulin resistance Mitochondrial biogenesis Obesity Parkinsonia aculeata |
topic |
AMPKα Herbal medicine Insulin resistance Mitochondrial biogenesis Obesity Parkinsonia aculeata |
description |
Ethnopharmacological relevance The search for natural agents that minimize obesity-associated disorders is receiving special attention. Parkinsonia aculeata L. (Caesalpineaceae) has long been used in Brazil as a hypoglycaemic herbal medicine, without any scientific basis. Aims of the study In this context, we aimed to use molecular and physiological methods to study the effect of a hydroethanolic extract partitioned with ethyl acetate from the aerial parts of Parkinsonia aculeata (HEPa/EtOAc) on insulin resistance in a mouse model of diet-induced obesity (DIO). Material and methods Firstly, C57BL/6J mice were fed either with standard rodent chow diet or a high-fat diet (HFD) for 12 consecutive weeks. Then, the animals were treated with HEPa/EtOAc at two doses (125 and 250 mg/kg/day) or metformin (200 mg/kg/day) for 16 days. At the end of the experiment, body weight, fat pad weight, fasting serum glucose (FSG), insulin (FSI) and leptin were measured. Homeostasis Model Assessment for Insulin Resistance (HOMA-IR) was also calculated. Glucose, insulin and pyruvate tolerance tests were performed. The expression and phosphorylation of IRβtyr, Aktser473, AMPKα and PGC1α in liver, muscle and adipose tissue were determined by Western blot analyses. Results Herein we demonstrate for the first time an improvement in insulin resistance following HEPa/EtOAc administration in obese mice, as shown by increased glucose, insulin and pyruvate tolerance, as well as an improvement in FSG, FSI, HOMA-IR and circulating leptin levels, which together are in part due to enhancement of the insulin signaling pathway in its main target tissues. Surprisingly, the increase in activation of the AMPKα-PGC1-α axis by HEPa/EtOAc was similar to that produced by metformin treatment in the liver and muscle tissues. Conclusion In conclusion, P. aculeata appears to be a source of therapeutic agent against obesity-related complications. |
publishDate |
2016 |
dc.date.none.fl_str_mv |
2016-05-13 2018-12-11T16:41:39Z 2018-12-11T16:41:39Z |
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/10.1016/j.jep.2016.02.048 Journal of Ethnopharmacology, v. 183, p. 95-102. 1872-7573 0378-8741 http://hdl.handle.net/11449/168528 10.1016/j.jep.2016.02.048 2-s2.0-84962309392 2-s2.0-84962309392.pdf |
url |
http://dx.doi.org/10.1016/j.jep.2016.02.048 http://hdl.handle.net/11449/168528 |
identifier_str_mv |
Journal of Ethnopharmacology, v. 183, p. 95-102. 1872-7573 0378-8741 10.1016/j.jep.2016.02.048 2-s2.0-84962309392 2-s2.0-84962309392.pdf |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Journal of Ethnopharmacology 1,150 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
95-102 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 |
|
_version_ |
1822182552560992256 |
dc.identifier.doi.none.fl_str_mv |
10.1016/j.jep.2016.02.048 |