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Age-dependent increase of etheno-DNA-adducts in liver and brain of ROS overproducing OXYS rats

Reactive oxygen species (ROS) and lipid peroxidation (LPO) play a role in aging and degenerative diseases. To correlate oxidative stress and LPO-derived DNA damage, we determined etheno-DNA-adducts in liver and brain from ROS overproducing OXYS rats in comparison with age-matched Wistar rats. Liver...

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Bibliographic Details
Main Authors: Nair, Jagadeesan (Author) , Bartsch, Helmut (Author)
Format: Article (Journal)
Language:English
Published: 24 August 2005
In: Biochemical and biophysical research communications
Year: 2005, Volume: 336, Issue: 2, Pages: 478-482
ISSN:1090-2104
DOI:10.1016/j.bbrc.2005.08.114
Online Access:Verlag, Volltext: https://doi.org/10.1016/j.bbrc.2005.08.114
Verlag, Volltext: http://www.sciencedirect.com/science/article/pii/S0006291X05018279
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Author Notes:Jagadeesan Nair, Olga Sinitsina, Elena A. Vasunina, Georgy A. Nevinsky, Jacques Laval, Helmut Bartsch
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Summary:Reactive oxygen species (ROS) and lipid peroxidation (LPO) play a role in aging and degenerative diseases. To correlate oxidative stress and LPO-derived DNA damage, we determined etheno-DNA-adducts in liver and brain from ROS overproducing OXYS rats in comparison with age-matched Wistar rats. Liver DNA samples from 3- and 15-month-old OXYS and Wistar rats were analyzed for 1,N6-ethenodeoxyadenosine (εdA) and 3,N4-ethenodeoxycytidine (εdC) by immunoaffinity/32P-postlabelling. While εdA and εdC levels were not different in young rats, adduct levels were significantly higher in old OXYS rats when compared to old Wistar or young OXYS rats. Frozen rat brain sections were analyzed for εdA by immunostaining of nuclei. Brains from old OXYS rats accumulated εdA more frequently than age-matched Wistar rats. Our results demonstrate increased LPO-induced DNA damage in organs of OXYS rats which correlates with their known shorter life-span and elevated frequency of chronic degenerative diseases.
Item Description:Gesehen am 07.12.2020
Physical Description:Online Resource
ISSN:1090-2104
DOI:10.1016/j.bbrc.2005.08.114

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