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Oral formulation of DPP-4 inhibitor plus Quercetin improves metabolic homeostasis in type 1 diabetic rats

This study aimed to investigate the potential of an oral formulation (QV formulation) containing Quercetin and a Dipeptidyl Peptidase-4 Inhibitor (DPP-4 inhibitor), Vildagliptin, in improving metabolic homeostasis in type 1 diabetes model. Female albino Fischer rats were divided into four groups: un...

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Autores principales: Miranda, Pedro Henrique de A., Lacerda, Kissyla Christine Duarte, Araújo, Carolina Morais, Barichello, José Mario, Lima, Wanderson Geraldo, Costa, Daniela Caldeira
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6192983/
https://www.ncbi.nlm.nih.gov/pubmed/30333575
http://dx.doi.org/10.1038/s41598-018-33727-x
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author Miranda, Pedro Henrique de A.
Lacerda, Kissyla Christine Duarte
Araújo, Carolina Morais
Barichello, José Mario
Lima, Wanderson Geraldo
Costa, Daniela Caldeira
author_facet Miranda, Pedro Henrique de A.
Lacerda, Kissyla Christine Duarte
Araújo, Carolina Morais
Barichello, José Mario
Lima, Wanderson Geraldo
Costa, Daniela Caldeira
author_sort Miranda, Pedro Henrique de A.
collection PubMed
description This study aimed to investigate the potential of an oral formulation (QV formulation) containing Quercetin and a Dipeptidyl Peptidase-4 Inhibitor (DPP-4 inhibitor), Vildagliptin, in improving metabolic homeostasis in type 1 diabetes model. Female albino Fischer rats were divided into four groups: untreated control animals (C), untreated diabetic animals (D), diabetic animals treated with QV formulation (DQV), and diabetic animals treated with insulin (DI). Diabetes was induced by injection of alloxan (135 mg kg body mass)(−1) and confirmed by glycemic test. After the 30-day treatment period, biochemical parameters were analyzed in the pancreas, liver, and serum. Histopathological changes in pancreatic tissue were examined by Hematoxyline & Eosin staining and the insulin content in the islet measured by immunohistochemistry with anti-insulin antibody. The glycogen content in the hepatocytes was quantified by Periodic Schiff Acid staining. The QV formulation reduced the glycemia, preserved the pancreatic architecture, increased insulin levels, furthermore ameliorated lipid profile and to promote higher survival rate of animals. Together, our data suggest that the QV formulation treatment was able to normalize metabolic homeostasis in type 1 diabetic rats.
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spelling pubmed-61929832018-10-23 Oral formulation of DPP-4 inhibitor plus Quercetin improves metabolic homeostasis in type 1 diabetic rats Miranda, Pedro Henrique de A. Lacerda, Kissyla Christine Duarte Araújo, Carolina Morais Barichello, José Mario Lima, Wanderson Geraldo Costa, Daniela Caldeira Sci Rep Article This study aimed to investigate the potential of an oral formulation (QV formulation) containing Quercetin and a Dipeptidyl Peptidase-4 Inhibitor (DPP-4 inhibitor), Vildagliptin, in improving metabolic homeostasis in type 1 diabetes model. Female albino Fischer rats were divided into four groups: untreated control animals (C), untreated diabetic animals (D), diabetic animals treated with QV formulation (DQV), and diabetic animals treated with insulin (DI). Diabetes was induced by injection of alloxan (135 mg kg body mass)(−1) and confirmed by glycemic test. After the 30-day treatment period, biochemical parameters were analyzed in the pancreas, liver, and serum. Histopathological changes in pancreatic tissue were examined by Hematoxyline & Eosin staining and the insulin content in the islet measured by immunohistochemistry with anti-insulin antibody. The glycogen content in the hepatocytes was quantified by Periodic Schiff Acid staining. The QV formulation reduced the glycemia, preserved the pancreatic architecture, increased insulin levels, furthermore ameliorated lipid profile and to promote higher survival rate of animals. Together, our data suggest that the QV formulation treatment was able to normalize metabolic homeostasis in type 1 diabetic rats. Nature Publishing Group UK 2018-10-17 /pmc/articles/PMC6192983/ /pubmed/30333575 http://dx.doi.org/10.1038/s41598-018-33727-x Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Miranda, Pedro Henrique de A.
Lacerda, Kissyla Christine Duarte
Araújo, Carolina Morais
Barichello, José Mario
Lima, Wanderson Geraldo
Costa, Daniela Caldeira
Oral formulation of DPP-4 inhibitor plus Quercetin improves metabolic homeostasis in type 1 diabetic rats
title Oral formulation of DPP-4 inhibitor plus Quercetin improves metabolic homeostasis in type 1 diabetic rats
title_full Oral formulation of DPP-4 inhibitor plus Quercetin improves metabolic homeostasis in type 1 diabetic rats
title_fullStr Oral formulation of DPP-4 inhibitor plus Quercetin improves metabolic homeostasis in type 1 diabetic rats
title_full_unstemmed Oral formulation of DPP-4 inhibitor plus Quercetin improves metabolic homeostasis in type 1 diabetic rats
title_short Oral formulation of DPP-4 inhibitor plus Quercetin improves metabolic homeostasis in type 1 diabetic rats
title_sort oral formulation of dpp-4 inhibitor plus quercetin improves metabolic homeostasis in type 1 diabetic rats
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6192983/
https://www.ncbi.nlm.nih.gov/pubmed/30333575
http://dx.doi.org/10.1038/s41598-018-33727-x
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