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Insulin action in adipose tissue in type 1 diabetes

BACKGROUND: Insulin action has been reported to be normal in type 1 diabetic patients. However, some studies have reported an insulin resistance state in these patients. The aim of this study was to investigate insulin resistance in a group of type 1 diabetic patients. We studied the insulin action...

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Autores principales: Arrieta-Blanco, Francisco, Botella-Carretero, Jose Ignacio, Iglesias, Pedro, Balsa, José Antonio, Zamarrón, Isabel, De la Puerta, Cristina, Arrieta, Juan José, Ramos, Francisco, Vázquez, Clotilde, Rovira, Adela
Formato: Texto
Lenguaje:English
Publicado: Dove Medical Press 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3068878/
https://www.ncbi.nlm.nih.gov/pubmed/21475629
http://dx.doi.org/10.2147/IJGM.S15809
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author Arrieta-Blanco, Francisco
Botella-Carretero, Jose Ignacio
Iglesias, Pedro
Balsa, José Antonio
Zamarrón, Isabel
De la Puerta, Cristina
Arrieta, Juan José
Ramos, Francisco
Vázquez, Clotilde
Rovira, Adela
author_facet Arrieta-Blanco, Francisco
Botella-Carretero, Jose Ignacio
Iglesias, Pedro
Balsa, José Antonio
Zamarrón, Isabel
De la Puerta, Cristina
Arrieta, Juan José
Ramos, Francisco
Vázquez, Clotilde
Rovira, Adela
author_sort Arrieta-Blanco, Francisco
collection PubMed
description BACKGROUND: Insulin action has been reported to be normal in type 1 diabetic patients. However, some studies have reported an insulin resistance state in these patients. The aim of this study was to investigate insulin resistance in a group of type 1 diabetic patients. We studied the insulin action in adipose tissue and analyzed the effects of duration of disease, body mass index (BMI), and glycosylated hemoglobin on insulin action at the receptor and postreceptor levels in adipocytes. METHODS: Nine female type 1 diabetic patients with different durations of disease and eight nondiabetic female patients of comparable age and BMI were studied. (125)I-insulin binding and U-[(14)C]-D-glucose transport was measured in a sample of subcutaneous gluteus adipose tissue obtained by open surgical biopsy from each subject. RESULTS: The duration of disease was negatively correlated with both (125)I-insulin binding capacity (r = −0.70, P < 0.05) and basal and maximum insulin-stimulated glucose transport (r = −0.87, P < 0.01, and r = −0.88, P < 0.01, respectively). Maximum specific (125)I-insulin binding to the receptors in adipocytes was higher in the group of patients with a shorter duration of disease (P < 0.01). Basal and maximum insulin-stimulated glucose transport was significantly higher in the group with less than 5 years of disease (P < 0.01). No correlation was found between BMI and insulin action. CONCLUSION: Female type 1 diabetic patients have normal insulin action. There is a high glucose uptake in the early phase of the disease, although a longer duration of disease appears to be a contributing factor to a decrease in insulin action in these patients, and involving both receptor and postreceptor mechanisms.
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spelling pubmed-30688782011-04-07 Insulin action in adipose tissue in type 1 diabetes Arrieta-Blanco, Francisco Botella-Carretero, Jose Ignacio Iglesias, Pedro Balsa, José Antonio Zamarrón, Isabel De la Puerta, Cristina Arrieta, Juan José Ramos, Francisco Vázquez, Clotilde Rovira, Adela Int J Gen Med Original Research BACKGROUND: Insulin action has been reported to be normal in type 1 diabetic patients. However, some studies have reported an insulin resistance state in these patients. The aim of this study was to investigate insulin resistance in a group of type 1 diabetic patients. We studied the insulin action in adipose tissue and analyzed the effects of duration of disease, body mass index (BMI), and glycosylated hemoglobin on insulin action at the receptor and postreceptor levels in adipocytes. METHODS: Nine female type 1 diabetic patients with different durations of disease and eight nondiabetic female patients of comparable age and BMI were studied. (125)I-insulin binding and U-[(14)C]-D-glucose transport was measured in a sample of subcutaneous gluteus adipose tissue obtained by open surgical biopsy from each subject. RESULTS: The duration of disease was negatively correlated with both (125)I-insulin binding capacity (r = −0.70, P < 0.05) and basal and maximum insulin-stimulated glucose transport (r = −0.87, P < 0.01, and r = −0.88, P < 0.01, respectively). Maximum specific (125)I-insulin binding to the receptors in adipocytes was higher in the group of patients with a shorter duration of disease (P < 0.01). Basal and maximum insulin-stimulated glucose transport was significantly higher in the group with less than 5 years of disease (P < 0.01). No correlation was found between BMI and insulin action. CONCLUSION: Female type 1 diabetic patients have normal insulin action. There is a high glucose uptake in the early phase of the disease, although a longer duration of disease appears to be a contributing factor to a decrease in insulin action in these patients, and involving both receptor and postreceptor mechanisms. Dove Medical Press 2011-02-22 /pmc/articles/PMC3068878/ /pubmed/21475629 http://dx.doi.org/10.2147/IJGM.S15809 Text en © 2011 Arrieta-Blanco et al, publisher and licensee Dove Medical Press Ltd. This is an Open Access article which permits unrestricted noncommercial use, provided the original work is properly cited.
spellingShingle Original Research
Arrieta-Blanco, Francisco
Botella-Carretero, Jose Ignacio
Iglesias, Pedro
Balsa, José Antonio
Zamarrón, Isabel
De la Puerta, Cristina
Arrieta, Juan José
Ramos, Francisco
Vázquez, Clotilde
Rovira, Adela
Insulin action in adipose tissue in type 1 diabetes
title Insulin action in adipose tissue in type 1 diabetes
title_full Insulin action in adipose tissue in type 1 diabetes
title_fullStr Insulin action in adipose tissue in type 1 diabetes
title_full_unstemmed Insulin action in adipose tissue in type 1 diabetes
title_short Insulin action in adipose tissue in type 1 diabetes
title_sort insulin action in adipose tissue in type 1 diabetes
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3068878/
https://www.ncbi.nlm.nih.gov/pubmed/21475629
http://dx.doi.org/10.2147/IJGM.S15809
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