| Literature DB >> 26890784 |
Ryszard Pluta1, Janusz Kocki2, Marzena Ułamek-Kozioł, Alicja Petniak2, Paulina Gil-Kulik2, Sławomir Januszewski1, Jacek Bogucki3, Mirosław Jabłoński4, Judyta Brzozowska5, Wanda Furmaga-Jabłońska6, Anna Bogucka-Kocka7, Stanisław J Czuczwar8.
Abstract
Brain ischemia may be causally related with Alzheimer's disease. Presumably, β-secretase and amyloid-β protein precursor gene expression changes may be associated with Alzheimer's disease neuropathology. Consequently, we have examined quantitative changes in both β-secretase and amyloid-β protein precursor genes in the medial temporal lobe cortex with the use of quantitative rtPCR analysis following 10-min global brain ischemia in rats with survival of 2, 7, and 30 days. The greatest significant overexpression of β-secretase gene was noted on the 2nd day, while on days 7-30 the expression of this gene was only modestly downregulated. Amyloid-β protein precursor gene was downregulated on the 2nd day, but on days 7-30 postischemia, there was a significant reverse tendency. Thus, the demonstrated alterations indicate that the considerable changes of expression of β-secretase and amyloid-β protein precursor genes may be connected with a response of neurons in medial temporal lobe cortex to transient global brain ischemia. Finally, the ischemia-induced gene changes may play a key role in a late and slow onset of Alzheimer-type pathology.Entities:
Keywords: Alzheimer’s disease; amyloid-β protein precursor; brain ischemia; dementia; temporal cortex; β-secretase
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Year: 2016 PMID: 26890784 DOI: 10.3233/JAD-151102
Source DB: PubMed Journal: J Alzheimers Dis ISSN: 1387-2877 Impact factor: 4.472