Literature DB >> 20880504

Astrocytes in Alzheimer's disease.

Alexei Verkhratsky1, Markel Olabarria, Harun N Noristani, Chia-Yu Yeh, Jose Julio Rodriguez.   

Abstract

The circuitry of the human brain is formed by neuronal networks embedded into astroglial syncytia. The astrocytes perform numerous functions, providing for the overall brain homeostasis, assisting in neurogenesis, determining the micro-architecture of the grey matter, and defending the brain through evolutionary conserved astrogliosis programs. Astroglial cells are engaged in neurological diseases by determining the progression and outcome of neuropathological process. Astrocytes are specifically involved in various neurodegenerative diseases, including Alzheimer's disease, amyotrophic lateral sclerosis, Parkinson's disease, and various forms of dementia. Recent evidence suggest that early stages of neurodegenerative processes are associated with atrophy of astroglia, which causes disruptions in synaptic connectivity, disbalance in neurotransmitter homeostasis, and neuronal death through increased excitotoxicity. At the later stages, astrocytes become activated and contribute to the neuroinflammatory component of neurodegeneration.
Copyright © 2010 The American Society for Experimental NeuroTherapeutics, Inc. Published by Elsevier Inc. All rights reserved.

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Year:  2010        PMID: 20880504      PMCID: PMC5084302          DOI: 10.1016/j.nurt.2010.05.017

Source DB:  PubMed          Journal:  Neurotherapeutics        ISSN: 1878-7479            Impact factor:   7.620


  205 in total

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5.  Concomitant astroglial atrophy and astrogliosis in a triple transgenic animal model of Alzheimer's disease.

Authors:  Markel Olabarria; Harun N Noristani; Alexei Verkhratsky; José J Rodríguez
Journal:  Glia       Date:  2010-05       Impact factor: 7.452

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  149 in total

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6.  Astrocytic changes with aging and Alzheimer's disease-type pathology in chimpanzees.

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8.  The Effects of Alpha Boswellic Acid on Reelin Expression and Tau Phosphorylation in Human Astrocytes.

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9.  ProNGF\NGF imbalance triggers learning and memory deficits, neurodegeneration and spontaneous epileptic-like discharges in transgenic mice.

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10.  KCa3.1 constitutes a pharmacological target for astrogliosis associated with Alzheimer's disease.

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