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Intranasal insulin in Alzheimer’s disease: Food for thought
Accumulating evidence suggests that disrupted brain insulin signaling promotes the development and progression of Alzheimer’s disease (AD), driving clinicians to target this circuitry. While both traditional and more modern antidiabetics show promise in combating insulin resistance, intranasal insul...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10523803/ https://www.ncbi.nlm.nih.gov/pubmed/29180222 http://dx.doi.org/10.1016/j.neuropharm.2017.11.037 |
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author | Chapman, Colin D. Schiöth, Helgi B. Grillo, Claudia A. Benedict, Christian |
author_facet | Chapman, Colin D. Schiöth, Helgi B. Grillo, Claudia A. Benedict, Christian |
author_sort | Chapman, Colin D. |
collection | PubMed |
description | Accumulating evidence suggests that disrupted brain insulin signaling promotes the development and progression of Alzheimer’s disease (AD), driving clinicians to target this circuitry. While both traditional and more modern antidiabetics show promise in combating insulin resistance, intranasal insulin appears to be the most efficient method of boosting brain insulin. Furthermore, intranasal delivery elegantly avoids adverse effects from peripheral insulin administration. However, there remain significant open questions regarding intranasal insulin’s efficacy, safety, and potential as an adjunct or mono-therapy. Thus, this review aims to critically evaluate the present evidence and future potential of intranasal insulin as a meaningful treatment for AD. This article is part of the Special Issue entitled ‘Metabolic Impairment as Risk Factors for Neurodegenerative Disorders.’ |
format | Online Article Text |
id | pubmed-10523803 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
record_format | MEDLINE/PubMed |
spelling | pubmed-105238032023-09-27 Intranasal insulin in Alzheimer’s disease: Food for thought Chapman, Colin D. Schiöth, Helgi B. Grillo, Claudia A. Benedict, Christian Neuropharmacology Article Accumulating evidence suggests that disrupted brain insulin signaling promotes the development and progression of Alzheimer’s disease (AD), driving clinicians to target this circuitry. While both traditional and more modern antidiabetics show promise in combating insulin resistance, intranasal insulin appears to be the most efficient method of boosting brain insulin. Furthermore, intranasal delivery elegantly avoids adverse effects from peripheral insulin administration. However, there remain significant open questions regarding intranasal insulin’s efficacy, safety, and potential as an adjunct or mono-therapy. Thus, this review aims to critically evaluate the present evidence and future potential of intranasal insulin as a meaningful treatment for AD. This article is part of the Special Issue entitled ‘Metabolic Impairment as Risk Factors for Neurodegenerative Disorders.’ 2018-07-01 2017-11-24 /pmc/articles/PMC10523803/ /pubmed/29180222 http://dx.doi.org/10.1016/j.neuropharm.2017.11.037 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) ). |
spellingShingle | Article Chapman, Colin D. Schiöth, Helgi B. Grillo, Claudia A. Benedict, Christian Intranasal insulin in Alzheimer’s disease: Food for thought |
title | Intranasal insulin in Alzheimer’s disease: Food for thought |
title_full | Intranasal insulin in Alzheimer’s disease: Food for thought |
title_fullStr | Intranasal insulin in Alzheimer’s disease: Food for thought |
title_full_unstemmed | Intranasal insulin in Alzheimer’s disease: Food for thought |
title_short | Intranasal insulin in Alzheimer’s disease: Food for thought |
title_sort | intranasal insulin in alzheimer’s disease: food for thought |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10523803/ https://www.ncbi.nlm.nih.gov/pubmed/29180222 http://dx.doi.org/10.1016/j.neuropharm.2017.11.037 |
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