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Chronic Neuroinflammation in Alzheimer’s Disease : New Perspectives on Animal Models and Promising Candidate Drugs
by
Rangel, Alejandra
, Gyengesi, Erika
, Münch, Gerald
, Karunaweera, Niloo
, Millington, Christopher
, Campbell, Iain L.
, Aldrich-Wright, Janice R.
, Sonego, Sandra
in
Alzheimer Disease - drug therapy
/ Alzheimer Disease - genetics
/ Alzheimer Disease - pathology
/ Alzheimer's disease
/ Amyloid beta-Peptides - metabolism
/ Animal cognition
/ Animals
/ Astrocytes - metabolism
/ Astrocytes - pathology
/ Brain
/ Clinical trials
/ Cytokines
/ Development and progression
/ Disease Models, Animal
/ Drug therapy
/ Glial Fibrillary Acidic Protein
/ Humans
/ Hypotheses
/ Inflammation
/ Inflammation - drug therapy
/ Inflammation - genetics
/ Inflammation - pathology
/ Interleukin-6 - genetics
/ Medical research
/ Medicine, Experimental
/ Mice
/ Mice, Transgenic
/ Nerve Tissue Proteins - genetics
/ Neurodegeneration
/ Proteins
/ Review
/ Rodents
/ Studies
2014
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Chronic Neuroinflammation in Alzheimer’s Disease : New Perspectives on Animal Models and Promising Candidate Drugs
by
Rangel, Alejandra
, Gyengesi, Erika
, Münch, Gerald
, Karunaweera, Niloo
, Millington, Christopher
, Campbell, Iain L.
, Aldrich-Wright, Janice R.
, Sonego, Sandra
in
Alzheimer Disease - drug therapy
/ Alzheimer Disease - genetics
/ Alzheimer Disease - pathology
/ Alzheimer's disease
/ Amyloid beta-Peptides - metabolism
/ Animal cognition
/ Animals
/ Astrocytes - metabolism
/ Astrocytes - pathology
/ Brain
/ Clinical trials
/ Cytokines
/ Development and progression
/ Disease Models, Animal
/ Drug therapy
/ Glial Fibrillary Acidic Protein
/ Humans
/ Hypotheses
/ Inflammation
/ Inflammation - drug therapy
/ Inflammation - genetics
/ Inflammation - pathology
/ Interleukin-6 - genetics
/ Medical research
/ Medicine, Experimental
/ Mice
/ Mice, Transgenic
/ Nerve Tissue Proteins - genetics
/ Neurodegeneration
/ Proteins
/ Review
/ Rodents
/ Studies
2014
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Chronic Neuroinflammation in Alzheimer’s Disease : New Perspectives on Animal Models and Promising Candidate Drugs
by
Rangel, Alejandra
, Gyengesi, Erika
, Münch, Gerald
, Karunaweera, Niloo
, Millington, Christopher
, Campbell, Iain L.
, Aldrich-Wright, Janice R.
, Sonego, Sandra
in
Alzheimer Disease - drug therapy
/ Alzheimer Disease - genetics
/ Alzheimer Disease - pathology
/ Alzheimer's disease
/ Amyloid beta-Peptides - metabolism
/ Animal cognition
/ Animals
/ Astrocytes - metabolism
/ Astrocytes - pathology
/ Brain
/ Clinical trials
/ Cytokines
/ Development and progression
/ Disease Models, Animal
/ Drug therapy
/ Glial Fibrillary Acidic Protein
/ Humans
/ Hypotheses
/ Inflammation
/ Inflammation - drug therapy
/ Inflammation - genetics
/ Inflammation - pathology
/ Interleukin-6 - genetics
/ Medical research
/ Medicine, Experimental
/ Mice
/ Mice, Transgenic
/ Nerve Tissue Proteins - genetics
/ Neurodegeneration
/ Proteins
/ Review
/ Rodents
/ Studies
2014
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Chronic Neuroinflammation in Alzheimer’s Disease : New Perspectives on Animal Models and Promising Candidate Drugs
Journal Article
Chronic Neuroinflammation in Alzheimer’s Disease : New Perspectives on Animal Models and Promising Candidate Drugs
2014
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Overview
Chronic neuroinflammation is now considered one of the major factors in the pathogenesis of Alzheimer’s disease (AD). However, the most widely used transgenic AD models (overexpressing mutated forms of amyloid precursor protein, presenilin, and/or tau) do not demonstrate the degree of inflammation, neurodegeneration (particularly of the cholinergic system), and cognitive decline that is comparable with the human disease. Hence a more suitable animal model is needed to more closely mimic the resulting cognitive decline and memory loss in humans in order to investigate the effects of neuroinflammation on neurodegeneration. One of these models is the glial fibrillary acidic protein-interleukin 6 (GFAP-IL6) mouse, in which chronic neuroinflammation triggered constitutive expression of the cytokine interleukin-6 (IL-6) in astrocytes. These transgenic mice show substantial and progressive neurodegeneration as well as a decline in motor skills and cognitive function, starting from 6 months of age. This animal model could serve as an excellent tool for drug discovery and validation in vivo. In this review, we have also selected three potential anti-inflammatory drugs, curcumin, apigenin, and tenilsetam, as candidate drugs, which could be tested in this model.
Publisher
Hindawi Puplishing Corporation,Hindawi Publishing Corporation,John Wiley & Sons, Inc
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