Nec-1 alleviates cognitive impairment with reduction of A and tau abnormalities in APP/PS1 mice

Authors
Yang, Seung-HoonLee, Dongkeun KennethShin, JisuLee, SejinBaek, SeungyeopKim, JiyoonJung, HoyongHah, Jung-MiKim, YoungSoo
Issue Date
2017-01
Publisher
WILEY
Citation
EMBO MOLECULAR MEDICINE, v.9, no.1, pp.61 - 77
Abstract
Alzheimer's disease (AD) is a neurodegenerative disorder characterized by cognitive symptoms of learning and memory deficits. Such cognitive impairments are attributed to brain atrophy resulting from progressive neuronal and synaptic loss; therefore, alleviation of neural cell death is as an important target of treatment as other classical hallmarks of AD, such as aggregation of amyloid- (A) and hyperphosphorylation of tau. Here, we found that an anti-necroptotic molecule necrostatin-1 (Nec-1) directly targets A and tau proteins, alleviates brain cell death and ameliorates cognitive impairment in AD models. In the cortex and hippocampus of APP/PS1 double-transgenic mice, Nec-1 treatment reduced the levels of A oligomers, plaques and hyperphosphorylated tau without affecting production of A, while it altered the levels of apoptotic marker proteins. Our results showing multiple beneficial modes of action of Nec-1 against AD provide evidence that Nec-1 may serve an important role in the development of preventive approach for AD.
Keywords
BETA-AMYLOID PEPTIDE; ALZHEIMERS-DISEASE; A-BETA; MOUSE MODEL; CELL-DEATH; HYPOTHETICAL MODEL; DIFFUSE PLAQUES; BRAIN ATROPHY; CROSS-LINKING; IN-VIVO; BETA-AMYLOID PEPTIDE; ALZHEIMERS-DISEASE; A-BETA; MOUSE MODEL; CELL-DEATH; HYPOTHETICAL MODEL; DIFFUSE PLAQUES; BRAIN ATROPHY; CROSS-LINKING; IN-VIVO; Alzheimer' s disease; A aggregation; cognitive deficit; necrostatin-1; tau hyperphosphorylation
ISSN
1757-4676
URI
https://pubs.kist.re.kr/handle/201004/123248
DOI
10.15252/emmm.201606566
Appears in Collections:
KIST Article > 2017
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