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Noradrenergic dysfunction in Alzheimer's disease

The brain noradrenergic system supplies the neurotransmitter norepinephrine throughout the brain via widespread efferent projections, and plays a pivotal role in modulating cognitive activities in the cortex. Profound noradrenergic degeneration in Alzheimer's disease (AD) patients has been obse...

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Autores principales: Gannon, Mary, Che, Pulin, Chen, Yunjia, Jiao, Kai, Roberson, Erik D., Wang, Qin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4469831/
https://www.ncbi.nlm.nih.gov/pubmed/26136654
http://dx.doi.org/10.3389/fnins.2015.00220
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author Gannon, Mary
Che, Pulin
Chen, Yunjia
Jiao, Kai
Roberson, Erik D.
Wang, Qin
author_facet Gannon, Mary
Che, Pulin
Chen, Yunjia
Jiao, Kai
Roberson, Erik D.
Wang, Qin
author_sort Gannon, Mary
collection PubMed
description The brain noradrenergic system supplies the neurotransmitter norepinephrine throughout the brain via widespread efferent projections, and plays a pivotal role in modulating cognitive activities in the cortex. Profound noradrenergic degeneration in Alzheimer's disease (AD) patients has been observed for decades, with recent research suggesting that the locus coeruleus (where noradrenergic neurons are mainly located) is a predominant site where AD-related pathology begins. Mounting evidence indicates that the loss of noradrenergic innervation greatly exacerbates AD pathogenesis and progression, although the precise roles of noradrenergic components in AD pathogenesis remain unclear. The aim of this review is to summarize current findings on noradrenergic dysfunction in AD, as well as to point out deficiencies in our knowledge where more research is needed.
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spelling pubmed-44698312015-07-01 Noradrenergic dysfunction in Alzheimer's disease Gannon, Mary Che, Pulin Chen, Yunjia Jiao, Kai Roberson, Erik D. Wang, Qin Front Neurosci Psychiatry The brain noradrenergic system supplies the neurotransmitter norepinephrine throughout the brain via widespread efferent projections, and plays a pivotal role in modulating cognitive activities in the cortex. Profound noradrenergic degeneration in Alzheimer's disease (AD) patients has been observed for decades, with recent research suggesting that the locus coeruleus (where noradrenergic neurons are mainly located) is a predominant site where AD-related pathology begins. Mounting evidence indicates that the loss of noradrenergic innervation greatly exacerbates AD pathogenesis and progression, although the precise roles of noradrenergic components in AD pathogenesis remain unclear. The aim of this review is to summarize current findings on noradrenergic dysfunction in AD, as well as to point out deficiencies in our knowledge where more research is needed. Frontiers Media S.A. 2015-06-17 /pmc/articles/PMC4469831/ /pubmed/26136654 http://dx.doi.org/10.3389/fnins.2015.00220 Text en Copyright © 2015 Gannon, Che, Chen, Jiao, Roberson and Wang. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Psychiatry
Gannon, Mary
Che, Pulin
Chen, Yunjia
Jiao, Kai
Roberson, Erik D.
Wang, Qin
Noradrenergic dysfunction in Alzheimer's disease
title Noradrenergic dysfunction in Alzheimer's disease
title_full Noradrenergic dysfunction in Alzheimer's disease
title_fullStr Noradrenergic dysfunction in Alzheimer's disease
title_full_unstemmed Noradrenergic dysfunction in Alzheimer's disease
title_short Noradrenergic dysfunction in Alzheimer's disease
title_sort noradrenergic dysfunction in alzheimer's disease
topic Psychiatry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4469831/
https://www.ncbi.nlm.nih.gov/pubmed/26136654
http://dx.doi.org/10.3389/fnins.2015.00220
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