| Literature DB >> 29614649 |
Giancarlo de Mattos Cardillo1, Vanessa de Jesus Rodrigues De-Paula1,2, Eliza Hiromi Ikenaga1, Luciana Rodrigues Costa1, Sergio Catanozi3, Evelin Lisete Schaeffer1, Wagner Farid Gattaz1, Daniel Shikanai Kerr1,4, Orestes Vicente Forlenza1.
Abstract
Telomere length (TL) is a biomarker of cell aging, and its shortening has been linked to several age-related diseases. In Alzheimer's disease (AD), telomere shortening has been associated with neuroinflammation and oxidative stress. The majority of studies on TL in AD were based on leucocyte DNA, with little information about its status in the central nervous system. In addition to other neuroprotective effects, lithium has been implicated in the maintenance of TL. The present study aims to determine the effect of chronic lithium treatment on TL in different regions of the mouse brain, using a triple-transgenic mouse model (3xTg-AD). Eighteen transgenic and 22 wild-type (Wt) male mice were treated for eight months with chow containing 1.0 g (Li1) or 2.0 g (Li2) of lithium carbonate/kg, or standard chow (Li0). DNA was extracted from parietal cortex, hippocampus and olfactory epithelium and TL was quantified by real-time PCR. Chronic lithium treatment was associated with longer telomeres in the hippocampus (Li2, p = 0.0159) and in the parietal cortex (Li1, p = 0.0375) of 3xTg-AD compared to Wt. Our findings suggest that chronic lithium treatment does affect telomere maintenance, but the magnitude and nature of this effect depend on the working concentrations of lithium and characteristics of the tissue. This effect was observed when comparing 3xTg-AD with Wt mice, suggesting that the presence of AD pathology was required for the lithium modulation of TL.Entities:
Keywords: Alzheimer’s disease; hippocampus; lithium; olfactory epithelium; parietal cortex; telomere; transgenic mice
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Year: 2018 PMID: 29614649 DOI: 10.3233/JAD-170838
Source DB: PubMed Journal: J Alzheimers Dis ISSN: 1387-2877 Impact factor: 4.472