| Literature DB >> 33671097 |
Ryszard Pluta1, Liang Ouyang2, Sławomir Januszewski1, Yang Li2, Stanisław J Czuczwar3.
Abstract
Recent evidence suggests that amyloid and tau protein are of vital importance in post-ischemic death of CA1 pyramidal neurons of the hippocampus. In this review, we summarize protein alterations associated with Alzheimer's disease and their gene expression (amyloid protein precursor and tau protein) after cerebral ischemia, as well as their roles in post-ischemic hippocampus neurodegeneration. In recent years, multiple studies aimed to elucidate the post-ischemic processes in the development of hippocampus neurodegeneration. Their findings have revealed the dysregulation of genes for amyloid protein precursor, β-secretase, presenilin 1 and 2, tau protein, autophagy, mitophagy, and apoptosis identical in nature to Alzheimer's disease. Herein, we present the latest data showing that amyloid and tau protein associated with Alzheimer's disease and their genes play a key role in post-ischemic neurodegeneration of the hippocampus with subsequent development of dementia. Therefore, understanding the underlying process for the development of post-ischemic CA1 area neurodegeneration in the hippocampus in conjunction with Alzheimer's disease-related proteins and genes will provide the most important therapeutic development goals to date.Entities:
Keywords: amyloid; amyloid plaques; brain ischemia; dementia; genes; hippocampus; neurodegeneration; neurofibrillary tangles; neuronal death; presenilin; secretases; tau protein; α-synuclein
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Year: 2021 PMID: 33671097 PMCID: PMC7957532 DOI: 10.3390/ijms22052460
Source DB: PubMed Journal: Int J Mol Sci ISSN: 1422-0067 Impact factor: 5.923