Pathology of nNOS-Expressing GABAergic Neurons in Mouse Model of Alzheimer's Disease. (1st August 2018)
- Record Type:
- Journal Article
- Title:
- Pathology of nNOS-Expressing GABAergic Neurons in Mouse Model of Alzheimer's Disease. (1st August 2018)
- Main Title:
- Pathology of nNOS-Expressing GABAergic Neurons in Mouse Model of Alzheimer's Disease
- Authors:
- Choi, Seungho
Won, Je-Seong
Carroll, Steven L.
Annamalai, Balasubramaniam
Singh, Inderjit
Singh, Avtar K. - Abstract:
- Graphical abstract: Highlights: APPSwDI transgenic mice develop early loss of GAD67 expression in CA1 of hippocampus. GAD67 + neurons exhibit high basal expression of nNOS and nitrosative stress. These neurons are highly vulnerable to Aβ due to the high intrinsic nitrosative stress. The loss of GAD67 + neurons correlates with cognitive and neuropsychiatric deficits. These suggest a role of nitrosative stress in of Alzheimer's GABAergic pathology. Abstract: Alzheimer's disease (AD) is the most common form of dementia that is often accompanied by mood and emotional disturbances and seizures. There is growing body of evidence that neurons expressing γ-aminobutyric acid (GABA) play an important role in regulation of cognition, mood, and emotion as well as seizure susceptibility, but participation of GABAergic neuronal pathology in Alzheimer's disease (AD) is not understood well at present. Here, we report that transgenic mice expressing human amyloid precursor protein Swedish–Dutch–Iowa mutant (APPSweDI ) exhibit early loss of neurons expressing GAD67, a GABA-synthesizing enzyme, in advance of the loss of pyramidal neurons in hippocampal CA1 region. The loss of GAD67 + neurons in APPSweDI mice accompanied with decreased spatial cognition as well as increased anxiety-like behaviors and kainic acid-induced seizure susceptibility at early phase. In the hippocampal CA1 region, GAD67 + neurons expressed high basal levels of neuronal nitric oxide synthase (nNOS) and nitrosative stressGraphical abstract: Highlights: APPSwDI transgenic mice develop early loss of GAD67 expression in CA1 of hippocampus. GAD67 + neurons exhibit high basal expression of nNOS and nitrosative stress. These neurons are highly vulnerable to Aβ due to the high intrinsic nitrosative stress. The loss of GAD67 + neurons correlates with cognitive and neuropsychiatric deficits. These suggest a role of nitrosative stress in of Alzheimer's GABAergic pathology. Abstract: Alzheimer's disease (AD) is the most common form of dementia that is often accompanied by mood and emotional disturbances and seizures. There is growing body of evidence that neurons expressing γ-aminobutyric acid (GABA) play an important role in regulation of cognition, mood, and emotion as well as seizure susceptibility, but participation of GABAergic neuronal pathology in Alzheimer's disease (AD) is not understood well at present. Here, we report that transgenic mice expressing human amyloid precursor protein Swedish–Dutch–Iowa mutant (APPSweDI ) exhibit early loss of neurons expressing GAD67, a GABA-synthesizing enzyme, in advance of the loss of pyramidal neurons in hippocampal CA1 region. The loss of GAD67 + neurons in APPSweDI mice accompanied with decreased spatial cognition as well as increased anxiety-like behaviors and kainic acid-induced seizure susceptibility at early phase. In the hippocampal CA1 region, GAD67 + neurons expressed high basal levels of neuronal nitric oxide synthase (nNOS) and nitrosative stress (nitrotyrosine). Similarly, GAD67 + neurons in primary cortical and hippocampal neuron cultures also expressed high basal levels of nNOS and degenerated in response to lower Aβ concentrations due to their high basal levels of nitrosative stress. Given the role of GABAergic neurons in cognitive and neuropsychiatric functions, this study reports the role of nNOS-mediated nitrosative stress in dysfunction of GABAergic neurons and its potential participation in early development of cognitive and neuropsychiatric symptoms in AD. … (more)
- Is Part Of:
- Neuroscience. Volume 384(2018)
- Journal:
- Neuroscience
- Issue:
- Volume 384(2018)
- Issue Display:
- Volume 384, Issue 2018 (2018)
- Year:
- 2018
- Volume:
- 384
- Issue:
- 2018
- Issue Sort Value:
- 2018-0384-2018-0000
- Page Start:
- 41
- Page End:
- 53
- Publication Date:
- 2018-08-01
- Subjects:
- AD Alzheimer's disease -- APPSweDI human amyloid precursor protein Swedish–Dutch–Iowa mutant -- Aβ amyloid-β -- GABA γ-aminobutyric acid -- KA kainic acid -- nNOS neuronal nitric oxide synthase -- NO nitric oxide -- NPLA Nω-Propyl-L-arginine hydrochloride -- NRGN neurogranin -- N-Tyr nitrotyrosine -- O2− superoxide anion -- ONOO− peroxynitrite -- RLD repeated low dose -- SIN-1 3-morpholinosydnonimine -- WT wild type
GABAergic neurons -- hippocampus -- nNOS -- nitrosative stress -- amyloid-β (Aβ)
Neurochemistry -- Periodicals
Neurophysiology -- Periodicals
Neurology -- Periodicals
Neurochimie -- Périodiques
Neurophysiologie -- Périodiques
Neurochemistry
Neurophysiology
Electronic journals
Periodicals
Electronic journals
612.8 - Journal URLs:
- http://www.sciencedirect.com/science/journal/03064522 ↗
http://www.clinicalkey.com/dura/browse/journalIssue/03064522 ↗
http://www.clinicalkey.com.au/dura/browse/journalIssue/03064522 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.neuroscience.2018.05.013 ↗
- Languages:
- English
- ISSNs:
- 0306-4522
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6081.559000
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