Article (Scientific journals)
Noradrenaline deficiency in brain increases beta-amyloid plaque burden in an animal model of Alzheimer's disease.
Kalinin, Sergey; Gavrilyuk, Vitaliy; Polak, Paul E et al.
2007In Neurobiology of Aging, 28 (8), p. 1206 - 1214
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Keywords :
Amyloid beta-Protein Precursor; Benzylamines; Neurotransmitter Uptake Inhibitors; Neprilysin; Isoproterenol; DSP 4; Norepinephrine; Alzheimer Disease/genetics; Alzheimer Disease/metabolism; Alzheimer Disease/pathology; Amyloid beta-Protein Precursor/genetics; Amyloid beta-Protein Precursor/metabolism; Animals; Animals, Newborn; Benzylamines/toxicity; Brain/pathology; Cells, Cultured; Disease Models, Animal; Dose-Response Relationship, Drug; Humans; Isoproterenol/pharmacology; Locus Coeruleus/drug effects; Locus Coeruleus/injuries; Locus Coeruleus/metabolism; Male; Mice; Mice, Inbred C57BL; Mice, Transgenic; Microglia/drug effects; Microglia/metabolism; Neprilysin/metabolism; Neurotransmitter Uptake Inhibitors/toxicity; Norepinephrine/deficiency; Norepinephrine/pharmacology; Phagocytosis/drug effects; Plaque, Amyloid/drug effects; Plaque, Amyloid/metabolism; Amyloid; Inflammation; Locus coeruleus; Nitric oxide; Noradrenaline; Neuroscience (all); Aging; Neurology (clinical); Developmental Biology; Geriatrics and Gerontology; General Neuroscience
Abstract :
[en] Loss of Locus coeruleus (LC) noradrenergic (NA) neurons occurs in several neurodegenerative conditions including Alzheimer's disease (AD). In vitro and in vivo studies have shown that NA influences several features of AD disease including inflammation, neurodegeneration, and cognitive function. In the current study we tested if LC loss influenced beta amyloid (Abeta) plaque deposition. LC neuronal degeneration was induced in transgenic mice expressing mutant V717F human amyloid precursor protein (APP) by treatment with the selective neurotoxin N-(2-chloroethyl)-N-ethyl-2-bromobenzylamine DSP4 (5mg/kg every 2 weeks beginning at age 3 months). At 9 months of age, when control mice show low amyloid load, DSP4-treated mice showed an approximately 5-fold increase in the average number of Abeta plaques. This was accompanied by an increase in the levels of APP C-terminal cleavage fragments. DSP4-treatment increased both microglial and astroglial activation. In vivo, DSP4-treatment decreased expression and activity of the Abeta degrading enzyme neprilysin, while in vitro NA increased phagocytosis of Abeta1-42 by microglia. These findings suggest that noradrenergic innervation from LC are needed to maintain adequate Abeta clearance, and therefore that LC degeneration could contribute to AD pathogenesis.
Disciplines :
Neurology
Author, co-author :
Kalinin, Sergey;  Department of Anesthesiology, University of Illinois, & Jesse Brown Veteran's Affairs Research Division, Chicago, IL 60612, United States
Gavrilyuk, Vitaliy;  Department of Anesthesiology, University of Illinois, Jesse Brown Veteran's Affairs Research Division, Chicago, IL 60612, United States
Polak, Paul E;  Department of Anesthesiology, University of Illinois, Jesse Brown Veteran's Affairs Research Division, Chicago, IL 60612, United States
Vasser, Robert;  Northwestern University, Chicago, IL 60611, United States
Zhao, Jie;  Northwestern University, Chicago, IL 60611, United States
HENEKA, Michael  ;  Department of Neurology, University of Muenster, Muenster, Germany
Feinstein, Douglas L;  Department of Anesthesiology, University of Illinois, Jesse Brown Veteran's Affairs Research Division, Chicago, IL 60612, United States
External co-authors :
yes
Language :
English
Title :
Noradrenaline deficiency in brain increases beta-amyloid plaque burden in an animal model of Alzheimer's disease.
Publication date :
August 2007
Journal title :
Neurobiology of Aging
ISSN :
0197-4580
eISSN :
1558-1497
Publisher :
Elsevier BV, United States
Volume :
28
Issue :
8
Pages :
1206 - 1214
Peer reviewed :
Peer Reviewed verified by ORBi
Funding text :
This work was funded in part by a VA MERIT grant (DLF), a grant from the American Alzheimer's Association (DLF) and from NIA (P01 AG021184, RV). We would like to thank Anthony Sharp for assistance with animal care, Dr. Elena Galea for assistance with histochemistry, and Dr. Cinzia Dello Russo for assistance with microglia preparation.
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