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IGF‐1 deficiency impairs neurovascular coupling in mice: implications for cerebromicrovascular aging

Aging is associated with marked deficiency in circulating IGF‐1, which has been shown to contribute to age‐related cognitive decline. Impairment of moment‐to‐moment adjustment of cerebral blood flow (CBF) via neurovascular coupling is thought to play a critical role in the genesis of age‐related cog...

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Autores principales: Toth, Peter, Tarantini, Stefano, Ashpole, Nicole M., Tucsek, Zsuzsanna, Milne, Ginger L., Valcarcel‐Ares, Noa M., Menyhart, Akos, Farkas, Eszter, Sonntag, William E., Csiszar, Anna, Ungvari, Zoltan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4693458/
https://www.ncbi.nlm.nih.gov/pubmed/26172407
http://dx.doi.org/10.1111/acel.12372
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author Toth, Peter
Tarantini, Stefano
Ashpole, Nicole M.
Tucsek, Zsuzsanna
Milne, Ginger L.
Valcarcel‐Ares, Noa M.
Menyhart, Akos
Farkas, Eszter
Sonntag, William E.
Csiszar, Anna
Ungvari, Zoltan
author_facet Toth, Peter
Tarantini, Stefano
Ashpole, Nicole M.
Tucsek, Zsuzsanna
Milne, Ginger L.
Valcarcel‐Ares, Noa M.
Menyhart, Akos
Farkas, Eszter
Sonntag, William E.
Csiszar, Anna
Ungvari, Zoltan
author_sort Toth, Peter
collection PubMed
description Aging is associated with marked deficiency in circulating IGF‐1, which has been shown to contribute to age‐related cognitive decline. Impairment of moment‐to‐moment adjustment of cerebral blood flow (CBF) via neurovascular coupling is thought to play a critical role in the genesis of age‐related cognitive impairment. To establish the link between IGF‐1 deficiency and cerebromicrovascular impairment, neurovascular coupling mechanisms were studied in a novel mouse model of IGF‐1 deficiency (Igf1 (f/f)‐TBG‐Cre‐AAV8) and accelerated vascular aging. We found that IGF‐1‐deficient mice exhibit neurovascular uncoupling and show a deficit in hippocampal‐dependent spatial memory test, mimicking the aging phenotype. IGF‐1 deficiency significantly impaired cerebromicrovascular endothelial function decreasing NO mediation of neurovascular coupling. IGF‐1 deficiency also impaired glutamate‐mediated CBF responses, likely due to dysregulation of astrocytic expression of metabotropic glutamate receptors and impairing mediation of CBF responses by eicosanoid gliotransmitters. Collectively, we demonstrate that IGF‐1 deficiency promotes cerebromicrovascular dysfunction and neurovascular uncoupling mimicking the aging phenotype, which are likely to contribute to cognitive impairment.
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spelling pubmed-46934582016-01-04 IGF‐1 deficiency impairs neurovascular coupling in mice: implications for cerebromicrovascular aging Toth, Peter Tarantini, Stefano Ashpole, Nicole M. Tucsek, Zsuzsanna Milne, Ginger L. Valcarcel‐Ares, Noa M. Menyhart, Akos Farkas, Eszter Sonntag, William E. Csiszar, Anna Ungvari, Zoltan Aging Cell Original Articles Aging is associated with marked deficiency in circulating IGF‐1, which has been shown to contribute to age‐related cognitive decline. Impairment of moment‐to‐moment adjustment of cerebral blood flow (CBF) via neurovascular coupling is thought to play a critical role in the genesis of age‐related cognitive impairment. To establish the link between IGF‐1 deficiency and cerebromicrovascular impairment, neurovascular coupling mechanisms were studied in a novel mouse model of IGF‐1 deficiency (Igf1 (f/f)‐TBG‐Cre‐AAV8) and accelerated vascular aging. We found that IGF‐1‐deficient mice exhibit neurovascular uncoupling and show a deficit in hippocampal‐dependent spatial memory test, mimicking the aging phenotype. IGF‐1 deficiency significantly impaired cerebromicrovascular endothelial function decreasing NO mediation of neurovascular coupling. IGF‐1 deficiency also impaired glutamate‐mediated CBF responses, likely due to dysregulation of astrocytic expression of metabotropic glutamate receptors and impairing mediation of CBF responses by eicosanoid gliotransmitters. Collectively, we demonstrate that IGF‐1 deficiency promotes cerebromicrovascular dysfunction and neurovascular uncoupling mimicking the aging phenotype, which are likely to contribute to cognitive impairment. John Wiley and Sons Inc. 2015-07-14 2015-12 /pmc/articles/PMC4693458/ /pubmed/26172407 http://dx.doi.org/10.1111/acel.12372 Text en © 2015 The Authors. Aging Cell published by the Anatomical Society and John Wiley & Sons Ltd. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Toth, Peter
Tarantini, Stefano
Ashpole, Nicole M.
Tucsek, Zsuzsanna
Milne, Ginger L.
Valcarcel‐Ares, Noa M.
Menyhart, Akos
Farkas, Eszter
Sonntag, William E.
Csiszar, Anna
Ungvari, Zoltan
IGF‐1 deficiency impairs neurovascular coupling in mice: implications for cerebromicrovascular aging
title IGF‐1 deficiency impairs neurovascular coupling in mice: implications for cerebromicrovascular aging
title_full IGF‐1 deficiency impairs neurovascular coupling in mice: implications for cerebromicrovascular aging
title_fullStr IGF‐1 deficiency impairs neurovascular coupling in mice: implications for cerebromicrovascular aging
title_full_unstemmed IGF‐1 deficiency impairs neurovascular coupling in mice: implications for cerebromicrovascular aging
title_short IGF‐1 deficiency impairs neurovascular coupling in mice: implications for cerebromicrovascular aging
title_sort igf‐1 deficiency impairs neurovascular coupling in mice: implications for cerebromicrovascular aging
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4693458/
https://www.ncbi.nlm.nih.gov/pubmed/26172407
http://dx.doi.org/10.1111/acel.12372
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