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Deficient hippocampal insulin signaling and augmented Tau phosphorylation is related to obesity- and age-induced peripheral insulin resistance: a study in Zucker rats

BACKGROUND: Insulin signaling and Tau protein phosphorylation in the hippocampi of young and old obese Zucker fa/fa rats and their lean controls were assessed to determine whether obesity-induced peripheral insulin resistance and aging are risk factors for central insulin resistance and whether cent...

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Autores principales: Špolcová, Andrea, Mikulášková, Barbora, Kršková, Katarína, Gajdošechová, Lucia, Zórad, Štefan, Olszanecki, Rafał, Suski, Maciej, Bujak-Giżycka, Beata, Železná, Blanka, Maletínská, Lenka
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4261609/
https://www.ncbi.nlm.nih.gov/pubmed/25257559
http://dx.doi.org/10.1186/1471-2202-15-111
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author Špolcová, Andrea
Mikulášková, Barbora
Kršková, Katarína
Gajdošechová, Lucia
Zórad, Štefan
Olszanecki, Rafał
Suski, Maciej
Bujak-Giżycka, Beata
Železná, Blanka
Maletínská, Lenka
author_facet Špolcová, Andrea
Mikulášková, Barbora
Kršková, Katarína
Gajdošechová, Lucia
Zórad, Štefan
Olszanecki, Rafał
Suski, Maciej
Bujak-Giżycka, Beata
Železná, Blanka
Maletínská, Lenka
author_sort Špolcová, Andrea
collection PubMed
description BACKGROUND: Insulin signaling and Tau protein phosphorylation in the hippocampi of young and old obese Zucker fa/fa rats and their lean controls were assessed to determine whether obesity-induced peripheral insulin resistance and aging are risk factors for central insulin resistance and whether central insulin resistance is related to the pathologic phosphorylation of the Tau protein. RESULTS: Aging and obesity significantly attenuated the phosphorylation of the insulin cascade kinases Akt (protein kinase B, PKB) and GSK-3β (glycogen synthase kinase 3β) in the hippocampi of the fa/fa rats. Furthermore, the hyperphosphorylation of Tau Ser396 alone and both Tau Ser396 and Thr231 was significantly augmented by aging and obesity, respectively, in the hippocampi of these rats. CONCLUSIONS: Both age-induced and obesity-induced peripheral insulin resistance are associated with central insulin resistance that is linked to hyperTau phosphorylation. Peripheral hyperinsulinemia, rather than hyperglycemia, appears to promote central insulin resistance and the Tau pathology in fa/fa rats.
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spelling pubmed-42616092014-12-10 Deficient hippocampal insulin signaling and augmented Tau phosphorylation is related to obesity- and age-induced peripheral insulin resistance: a study in Zucker rats Špolcová, Andrea Mikulášková, Barbora Kršková, Katarína Gajdošechová, Lucia Zórad, Štefan Olszanecki, Rafał Suski, Maciej Bujak-Giżycka, Beata Železná, Blanka Maletínská, Lenka BMC Neurosci Research Article BACKGROUND: Insulin signaling and Tau protein phosphorylation in the hippocampi of young and old obese Zucker fa/fa rats and their lean controls were assessed to determine whether obesity-induced peripheral insulin resistance and aging are risk factors for central insulin resistance and whether central insulin resistance is related to the pathologic phosphorylation of the Tau protein. RESULTS: Aging and obesity significantly attenuated the phosphorylation of the insulin cascade kinases Akt (protein kinase B, PKB) and GSK-3β (glycogen synthase kinase 3β) in the hippocampi of the fa/fa rats. Furthermore, the hyperphosphorylation of Tau Ser396 alone and both Tau Ser396 and Thr231 was significantly augmented by aging and obesity, respectively, in the hippocampi of these rats. CONCLUSIONS: Both age-induced and obesity-induced peripheral insulin resistance are associated with central insulin resistance that is linked to hyperTau phosphorylation. Peripheral hyperinsulinemia, rather than hyperglycemia, appears to promote central insulin resistance and the Tau pathology in fa/fa rats. BioMed Central 2014-09-25 /pmc/articles/PMC4261609/ /pubmed/25257559 http://dx.doi.org/10.1186/1471-2202-15-111 Text en © Špolcová et al.; licensee BioMed Central Ltd. 2014 This article is published under license to BioMed Central Ltd. 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 credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Špolcová, Andrea
Mikulášková, Barbora
Kršková, Katarína
Gajdošechová, Lucia
Zórad, Štefan
Olszanecki, Rafał
Suski, Maciej
Bujak-Giżycka, Beata
Železná, Blanka
Maletínská, Lenka
Deficient hippocampal insulin signaling and augmented Tau phosphorylation is related to obesity- and age-induced peripheral insulin resistance: a study in Zucker rats
title Deficient hippocampal insulin signaling and augmented Tau phosphorylation is related to obesity- and age-induced peripheral insulin resistance: a study in Zucker rats
title_full Deficient hippocampal insulin signaling and augmented Tau phosphorylation is related to obesity- and age-induced peripheral insulin resistance: a study in Zucker rats
title_fullStr Deficient hippocampal insulin signaling and augmented Tau phosphorylation is related to obesity- and age-induced peripheral insulin resistance: a study in Zucker rats
title_full_unstemmed Deficient hippocampal insulin signaling and augmented Tau phosphorylation is related to obesity- and age-induced peripheral insulin resistance: a study in Zucker rats
title_short Deficient hippocampal insulin signaling and augmented Tau phosphorylation is related to obesity- and age-induced peripheral insulin resistance: a study in Zucker rats
title_sort deficient hippocampal insulin signaling and augmented tau phosphorylation is related to obesity- and age-induced peripheral insulin resistance: a study in zucker rats
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4261609/
https://www.ncbi.nlm.nih.gov/pubmed/25257559
http://dx.doi.org/10.1186/1471-2202-15-111
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