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Curcumin regulates insulin pathways and glucose metabolism in the brains of APPswe/PS1dE9 mice
Recent studies have shown the therapeutic potential of curcumin in Alzheimer’s disease (AD). In 2014, our lab found that curcumin reduced Aβ40, Aβ42 and Aβ-derived diffusible ligands in the mouse hippocampus, and improved learning and memory. However, the mechanisms underlying this biological effect...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5806780/ https://www.ncbi.nlm.nih.gov/pubmed/28124574 http://dx.doi.org/10.1177/0394632016688025 |
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author | Wang, Pengwen Su, Caixin Feng, Huili Chen, Xiaopei Dong, Yunfang Rao, Yingxue Ren, Ying Yang, Jinduo Shi, Jing Tian, Jinzhou Jiang, Shucui |
author_facet | Wang, Pengwen Su, Caixin Feng, Huili Chen, Xiaopei Dong, Yunfang Rao, Yingxue Ren, Ying Yang, Jinduo Shi, Jing Tian, Jinzhou Jiang, Shucui |
author_sort | Wang, Pengwen |
collection | PubMed |
description | Recent studies have shown the therapeutic potential of curcumin in Alzheimer’s disease (AD). In 2014, our lab found that curcumin reduced Aβ40, Aβ42 and Aβ-derived diffusible ligands in the mouse hippocampus, and improved learning and memory. However, the mechanisms underlying this biological effect are only partially known. There is considerable evidence in brain metabolism studies indicating that AD might be a brain-specific type of diabetes with progressive impairment of glucose utilisation and insulin signalling. We hypothesised that curcumin might target both the glucose metabolism and insulin signalling pathways. In this study, we monitored brain glucose metabolism in living APPswe/PS1dE9 double transgenic mice using a micro-positron emission tomography (PET) technique. The study showed an improvement in cerebral glucose uptake in AD mice. For a more in-depth study, we used immunohistochemical (IHC) staining and western blot techniques to examine key factors in both glucose metabolism and brain insulin signalling pathways. The results showed that curcumin ameliorated the defective insulin signalling pathway by upregulating insulin-like growth factor (IGF)-1R, IRS-2, PI3K, p-PI3K, Akt and p-Akt protein expression while downregulating IR and IRS-1. Our study found that curcumin improved spatial learning and memory, at least in part, by increasing glucose metabolism and ameliorating the impaired insulin signalling pathways in the brain. |
format | Online Article Text |
id | pubmed-5806780 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-58067802018-02-28 Curcumin regulates insulin pathways and glucose metabolism in the brains of APPswe/PS1dE9 mice Wang, Pengwen Su, Caixin Feng, Huili Chen, Xiaopei Dong, Yunfang Rao, Yingxue Ren, Ying Yang, Jinduo Shi, Jing Tian, Jinzhou Jiang, Shucui Int J Immunopathol Pharmacol Original Articles Recent studies have shown the therapeutic potential of curcumin in Alzheimer’s disease (AD). In 2014, our lab found that curcumin reduced Aβ40, Aβ42 and Aβ-derived diffusible ligands in the mouse hippocampus, and improved learning and memory. However, the mechanisms underlying this biological effect are only partially known. There is considerable evidence in brain metabolism studies indicating that AD might be a brain-specific type of diabetes with progressive impairment of glucose utilisation and insulin signalling. We hypothesised that curcumin might target both the glucose metabolism and insulin signalling pathways. In this study, we monitored brain glucose metabolism in living APPswe/PS1dE9 double transgenic mice using a micro-positron emission tomography (PET) technique. The study showed an improvement in cerebral glucose uptake in AD mice. For a more in-depth study, we used immunohistochemical (IHC) staining and western blot techniques to examine key factors in both glucose metabolism and brain insulin signalling pathways. The results showed that curcumin ameliorated the defective insulin signalling pathway by upregulating insulin-like growth factor (IGF)-1R, IRS-2, PI3K, p-PI3K, Akt and p-Akt protein expression while downregulating IR and IRS-1. Our study found that curcumin improved spatial learning and memory, at least in part, by increasing glucose metabolism and ameliorating the impaired insulin signalling pathways in the brain. SAGE Publications 2017-01-26 2017-03 /pmc/articles/PMC5806780/ /pubmed/28124574 http://dx.doi.org/10.1177/0394632016688025 Text en © The Author(s) 2017 http://creativecommons.org/licenses/by-nc/3.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 3.0 License (http://www.creativecommons.org/licenses/by-nc/3.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access page(https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Original Articles Wang, Pengwen Su, Caixin Feng, Huili Chen, Xiaopei Dong, Yunfang Rao, Yingxue Ren, Ying Yang, Jinduo Shi, Jing Tian, Jinzhou Jiang, Shucui Curcumin regulates insulin pathways and glucose metabolism in the brains of APPswe/PS1dE9 mice |
title | Curcumin regulates insulin pathways and glucose metabolism in the brains of APPswe/PS1dE9 mice |
title_full | Curcumin regulates insulin pathways and glucose metabolism in the brains of APPswe/PS1dE9 mice |
title_fullStr | Curcumin regulates insulin pathways and glucose metabolism in the brains of APPswe/PS1dE9 mice |
title_full_unstemmed | Curcumin regulates insulin pathways and glucose metabolism in the brains of APPswe/PS1dE9 mice |
title_short | Curcumin regulates insulin pathways and glucose metabolism in the brains of APPswe/PS1dE9 mice |
title_sort | curcumin regulates insulin pathways and glucose metabolism in the brains of appswe/ps1de9 mice |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5806780/ https://www.ncbi.nlm.nih.gov/pubmed/28124574 http://dx.doi.org/10.1177/0394632016688025 |
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