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Changes in the Expression of Insulin Pathway, Neutrophil Elastase and Alpha 1 Antitrypsin Genes from Leukocytes of Young Individuals with Insulin Resistance

BACKGROUND: Chronic hyperinsulinemia is a hallmark of insulin resistance that affects a diversity of cells, including leukocytes modifying the expression of some genes involved in insulin signaling. PURPOSE: The aim of this study was to evaluate how hyperinsulinemia affects the expression of genes i...

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Autores principales: Cruz-Pineda, Walter David, Garibay-Cerdenares, Olga Lilia, Rodríguez-Ruíz, Hugo Alberto, Matia-García, Inés, Marino-Ortega, Linda Anahí, Espinoza-Rojo, Mónica, Reyes-Castillo, Zyanya, Castro-Alarcón, Natividad, Castañeda-Saucedo, Eduardo, Illades-Aguiar, Berenice, Parra-Rojas, Isela
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9215908/
https://www.ncbi.nlm.nih.gov/pubmed/35757193
http://dx.doi.org/10.2147/DMSO.S362881
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author Cruz-Pineda, Walter David
Garibay-Cerdenares, Olga Lilia
Rodríguez-Ruíz, Hugo Alberto
Matia-García, Inés
Marino-Ortega, Linda Anahí
Espinoza-Rojo, Mónica
Reyes-Castillo, Zyanya
Castro-Alarcón, Natividad
Castañeda-Saucedo, Eduardo
Illades-Aguiar, Berenice
Parra-Rojas, Isela
author_facet Cruz-Pineda, Walter David
Garibay-Cerdenares, Olga Lilia
Rodríguez-Ruíz, Hugo Alberto
Matia-García, Inés
Marino-Ortega, Linda Anahí
Espinoza-Rojo, Mónica
Reyes-Castillo, Zyanya
Castro-Alarcón, Natividad
Castañeda-Saucedo, Eduardo
Illades-Aguiar, Berenice
Parra-Rojas, Isela
author_sort Cruz-Pineda, Walter David
collection PubMed
description BACKGROUND: Chronic hyperinsulinemia is a hallmark of insulin resistance that affects a diversity of cells, including leukocytes modifying the expression of some genes involved in insulin signaling. PURPOSE: The aim of this study was to evaluate how hyperinsulinemia affects the expression of genes involved in the proximal insulin signaling pathway in leukocytes from 45 young individuals grouped: normal weight with not insulin resistance (NIR), with insulin resistance (IR) and with obesity (OB-IR). METHODS: qPCR was performed to analyze the expression of insulin receptor (INSR), insulin receptor substrate 1 and 2 (IRS-1 and IRS-2), neutrophil elastase (NE), alpha 1 antitrypsin (A1AT), glucose transporters 1, 3 and 4 (GLUT-1, GLUT-3 and GLUT-4) by the 2(−ΔCt) method, and the correlation between the genes was determined by Spearman’s test. RESULTS: The mRNA expression analysis of all genes between NIR and IR individuals revealed no differences. However, when comparing NIR and IR individuals with OB-IR, an increase in NE and A1AT expression and a clear trend towards a decrease in IRS-2 expression was observed, whereas the comparison of IR and OB-IR showed a decrease in GLUT-3 expression. Overall, the correlation analysis showed that in the IR group there was a positive correlation only between NE with IRS-1 (r = 0.72, p = 0.003), while in the OB-IR group, there was a positive correlation between the NE and A1AT with INSR (r = 0.62, p = 0.01 and r = 0.74, p = 0.002, respectively) and with IRS-2 (r = 0.74, p = 0.002 and r = 0.76, p = 0.001, respectively). CONCLUSION: These results suggest that hyperinsulinemia and obesity are associated with changes in the expression of genes in leukocytes involved in the insulin pathway that are related to NE and A1AT.
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spelling pubmed-92159082022-06-23 Changes in the Expression of Insulin Pathway, Neutrophil Elastase and Alpha 1 Antitrypsin Genes from Leukocytes of Young Individuals with Insulin Resistance Cruz-Pineda, Walter David Garibay-Cerdenares, Olga Lilia Rodríguez-Ruíz, Hugo Alberto Matia-García, Inés Marino-Ortega, Linda Anahí Espinoza-Rojo, Mónica Reyes-Castillo, Zyanya Castro-Alarcón, Natividad Castañeda-Saucedo, Eduardo Illades-Aguiar, Berenice Parra-Rojas, Isela Diabetes Metab Syndr Obes Original Research BACKGROUND: Chronic hyperinsulinemia is a hallmark of insulin resistance that affects a diversity of cells, including leukocytes modifying the expression of some genes involved in insulin signaling. PURPOSE: The aim of this study was to evaluate how hyperinsulinemia affects the expression of genes involved in the proximal insulin signaling pathway in leukocytes from 45 young individuals grouped: normal weight with not insulin resistance (NIR), with insulin resistance (IR) and with obesity (OB-IR). METHODS: qPCR was performed to analyze the expression of insulin receptor (INSR), insulin receptor substrate 1 and 2 (IRS-1 and IRS-2), neutrophil elastase (NE), alpha 1 antitrypsin (A1AT), glucose transporters 1, 3 and 4 (GLUT-1, GLUT-3 and GLUT-4) by the 2(−ΔCt) method, and the correlation between the genes was determined by Spearman’s test. RESULTS: The mRNA expression analysis of all genes between NIR and IR individuals revealed no differences. However, when comparing NIR and IR individuals with OB-IR, an increase in NE and A1AT expression and a clear trend towards a decrease in IRS-2 expression was observed, whereas the comparison of IR and OB-IR showed a decrease in GLUT-3 expression. Overall, the correlation analysis showed that in the IR group there was a positive correlation only between NE with IRS-1 (r = 0.72, p = 0.003), while in the OB-IR group, there was a positive correlation between the NE and A1AT with INSR (r = 0.62, p = 0.01 and r = 0.74, p = 0.002, respectively) and with IRS-2 (r = 0.74, p = 0.002 and r = 0.76, p = 0.001, respectively). CONCLUSION: These results suggest that hyperinsulinemia and obesity are associated with changes in the expression of genes in leukocytes involved in the insulin pathway that are related to NE and A1AT. Dove 2022-06-18 /pmc/articles/PMC9215908/ /pubmed/35757193 http://dx.doi.org/10.2147/DMSO.S362881 Text en © 2022 Cruz-Pineda et al. https://creativecommons.org/licenses/by-nc/3.0/This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/ (https://creativecommons.org/licenses/by-nc/3.0/) ). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Original Research
Cruz-Pineda, Walter David
Garibay-Cerdenares, Olga Lilia
Rodríguez-Ruíz, Hugo Alberto
Matia-García, Inés
Marino-Ortega, Linda Anahí
Espinoza-Rojo, Mónica
Reyes-Castillo, Zyanya
Castro-Alarcón, Natividad
Castañeda-Saucedo, Eduardo
Illades-Aguiar, Berenice
Parra-Rojas, Isela
Changes in the Expression of Insulin Pathway, Neutrophil Elastase and Alpha 1 Antitrypsin Genes from Leukocytes of Young Individuals with Insulin Resistance
title Changes in the Expression of Insulin Pathway, Neutrophil Elastase and Alpha 1 Antitrypsin Genes from Leukocytes of Young Individuals with Insulin Resistance
title_full Changes in the Expression of Insulin Pathway, Neutrophil Elastase and Alpha 1 Antitrypsin Genes from Leukocytes of Young Individuals with Insulin Resistance
title_fullStr Changes in the Expression of Insulin Pathway, Neutrophil Elastase and Alpha 1 Antitrypsin Genes from Leukocytes of Young Individuals with Insulin Resistance
title_full_unstemmed Changes in the Expression of Insulin Pathway, Neutrophil Elastase and Alpha 1 Antitrypsin Genes from Leukocytes of Young Individuals with Insulin Resistance
title_short Changes in the Expression of Insulin Pathway, Neutrophil Elastase and Alpha 1 Antitrypsin Genes from Leukocytes of Young Individuals with Insulin Resistance
title_sort changes in the expression of insulin pathway, neutrophil elastase and alpha 1 antitrypsin genes from leukocytes of young individuals with insulin resistance
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9215908/
https://www.ncbi.nlm.nih.gov/pubmed/35757193
http://dx.doi.org/10.2147/DMSO.S362881
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