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Insulin signaling pathways in a patient with insulin resistance of difficult management - a case report

Insulin signalling pathways were investigated in a 33 year-old woman with immunologic insulin resistance. Her past medical history was remarkable for intermittent use of insulin and allergic reactions to several drugs, and measure of plasma anti-insulin antibodies level corroborated the clinical sus...

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Autores principales: Taboada, Giselle F, de Freitas, Marta S, da S Corrêa, Fernanda H, Junior, Carlos RMA, de B Gomes, Marília
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2789034/
https://www.ncbi.nlm.nih.gov/pubmed/19941665
http://dx.doi.org/10.1186/1758-5996-1-23
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author Taboada, Giselle F
de Freitas, Marta S
da S Corrêa, Fernanda H
Junior, Carlos RMA
de B Gomes, Marília
author_facet Taboada, Giselle F
de Freitas, Marta S
da S Corrêa, Fernanda H
Junior, Carlos RMA
de B Gomes, Marília
author_sort Taboada, Giselle F
collection PubMed
description Insulin signalling pathways were investigated in a 33 year-old woman with immunologic insulin resistance. Her past medical history was remarkable for intermittent use of insulin and allergic reactions to several drugs, and measure of plasma anti-insulin antibodies level corroborated the clinical suspicion of immune mediated insulin resistance (8074 nU/ml - RIA - Ref value: <60). Treatment with several immunosuppressive regimens was tried, however the results were disappointing. Possible subcellular mechanisms of insulin resistance were investigated by performing analysis of insulin receptor and post receptor signaling in skeletal muscle biopsy. The expression of insulin receptor (IR), insulin receptor substrate 1 (IRS-1) and glucose transporter 4 (GLUT-4) was evaluated in total extract from muscle tissue by Western blotting. Basal IR, IRS-1 and GLUT-4 expression was detected, however receptor autophosphorylation was not observed. A study of translocation of GLUT-4 to plasma membrane showed that tissue presented low levels of membrane-associated GLUT-4. When in vitro stimulation was undertaken, tissue was capable to be responsive to insulin. Our results suggest that even though IR expression was normally occurring, IR β-subunit tyrosine kinase activity in muscle was down-regulated leading to alterations in insulin post receptor signaling. Consistent with normal insulin receptor and post receptor signaling, our results were compatible with decreased insulin binding to IR probably due to neutralization by anti-insulin antibodies. In conclusion, this patient has immunologic insulin resistance and treatment should be based on immunosuppressive drugs as tolerated.
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spelling pubmed-27890342009-12-05 Insulin signaling pathways in a patient with insulin resistance of difficult management - a case report Taboada, Giselle F de Freitas, Marta S da S Corrêa, Fernanda H Junior, Carlos RMA de B Gomes, Marília Diabetol Metab Syndr Short Report Insulin signalling pathways were investigated in a 33 year-old woman with immunologic insulin resistance. Her past medical history was remarkable for intermittent use of insulin and allergic reactions to several drugs, and measure of plasma anti-insulin antibodies level corroborated the clinical suspicion of immune mediated insulin resistance (8074 nU/ml - RIA - Ref value: <60). Treatment with several immunosuppressive regimens was tried, however the results were disappointing. Possible subcellular mechanisms of insulin resistance were investigated by performing analysis of insulin receptor and post receptor signaling in skeletal muscle biopsy. The expression of insulin receptor (IR), insulin receptor substrate 1 (IRS-1) and glucose transporter 4 (GLUT-4) was evaluated in total extract from muscle tissue by Western blotting. Basal IR, IRS-1 and GLUT-4 expression was detected, however receptor autophosphorylation was not observed. A study of translocation of GLUT-4 to plasma membrane showed that tissue presented low levels of membrane-associated GLUT-4. When in vitro stimulation was undertaken, tissue was capable to be responsive to insulin. Our results suggest that even though IR expression was normally occurring, IR β-subunit tyrosine kinase activity in muscle was down-regulated leading to alterations in insulin post receptor signaling. Consistent with normal insulin receptor and post receptor signaling, our results were compatible with decreased insulin binding to IR probably due to neutralization by anti-insulin antibodies. In conclusion, this patient has immunologic insulin resistance and treatment should be based on immunosuppressive drugs as tolerated. BioMed Central 2009-11-26 /pmc/articles/PMC2789034/ /pubmed/19941665 http://dx.doi.org/10.1186/1758-5996-1-23 Text en Copyright ©2009 Taboada et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Short Report
Taboada, Giselle F
de Freitas, Marta S
da S Corrêa, Fernanda H
Junior, Carlos RMA
de B Gomes, Marília
Insulin signaling pathways in a patient with insulin resistance of difficult management - a case report
title Insulin signaling pathways in a patient with insulin resistance of difficult management - a case report
title_full Insulin signaling pathways in a patient with insulin resistance of difficult management - a case report
title_fullStr Insulin signaling pathways in a patient with insulin resistance of difficult management - a case report
title_full_unstemmed Insulin signaling pathways in a patient with insulin resistance of difficult management - a case report
title_short Insulin signaling pathways in a patient with insulin resistance of difficult management - a case report
title_sort insulin signaling pathways in a patient with insulin resistance of difficult management - a case report
topic Short Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2789034/
https://www.ncbi.nlm.nih.gov/pubmed/19941665
http://dx.doi.org/10.1186/1758-5996-1-23
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