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Changes in insulin and insulin signaling in Alzheimer’s disease: cause or consequence?
Individuals with type 2 diabetes have an increased risk for developing Alzheimer’s disease (AD), although the causal relationship remains poorly understood. Alterations in insulin signaling (IS) are reported in the AD brain. Moreover, oligomers/fibrils of amyloid-β (Aβ) can lead to neuronal insulin...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Rockefeller University Press
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4986537/ https://www.ncbi.nlm.nih.gov/pubmed/27432942 http://dx.doi.org/10.1084/jem.20160493 |
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author | Stanley, Molly Macauley, Shannon L. Holtzman, David M. |
author_facet | Stanley, Molly Macauley, Shannon L. Holtzman, David M. |
author_sort | Stanley, Molly |
collection | PubMed |
description | Individuals with type 2 diabetes have an increased risk for developing Alzheimer’s disease (AD), although the causal relationship remains poorly understood. Alterations in insulin signaling (IS) are reported in the AD brain. Moreover, oligomers/fibrils of amyloid-β (Aβ) can lead to neuronal insulin resistance and intranasal insulin is being explored as a potential therapy for AD. Conversely, elevated insulin levels (ins) are found in AD patients and high insulin has been reported to increase Aβ levels and tau phosphorylation, which could exacerbate AD pathology. Herein, we explore whether changes in ins and IS are a cause or consequence of AD. |
format | Online Article Text |
id | pubmed-4986537 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-49865372017-01-25 Changes in insulin and insulin signaling in Alzheimer’s disease: cause or consequence? Stanley, Molly Macauley, Shannon L. Holtzman, David M. J Exp Med Reviews Individuals with type 2 diabetes have an increased risk for developing Alzheimer’s disease (AD), although the causal relationship remains poorly understood. Alterations in insulin signaling (IS) are reported in the AD brain. Moreover, oligomers/fibrils of amyloid-β (Aβ) can lead to neuronal insulin resistance and intranasal insulin is being explored as a potential therapy for AD. Conversely, elevated insulin levels (ins) are found in AD patients and high insulin has been reported to increase Aβ levels and tau phosphorylation, which could exacerbate AD pathology. Herein, we explore whether changes in ins and IS are a cause or consequence of AD. The Rockefeller University Press 2016-07-25 /pmc/articles/PMC4986537/ /pubmed/27432942 http://dx.doi.org/10.1084/jem.20160493 Text en © 2016 Stanley et al. This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 3.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/3.0/). |
spellingShingle | Reviews Stanley, Molly Macauley, Shannon L. Holtzman, David M. Changes in insulin and insulin signaling in Alzheimer’s disease: cause or consequence? |
title | Changes in insulin and insulin signaling in Alzheimer’s disease:
cause or consequence? |
title_full | Changes in insulin and insulin signaling in Alzheimer’s disease:
cause or consequence? |
title_fullStr | Changes in insulin and insulin signaling in Alzheimer’s disease:
cause or consequence? |
title_full_unstemmed | Changes in insulin and insulin signaling in Alzheimer’s disease:
cause or consequence? |
title_short | Changes in insulin and insulin signaling in Alzheimer’s disease:
cause or consequence? |
title_sort | changes in insulin and insulin signaling in alzheimer’s disease:
cause or consequence? |
topic | Reviews |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4986537/ https://www.ncbi.nlm.nih.gov/pubmed/27432942 http://dx.doi.org/10.1084/jem.20160493 |
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