TY - JOUR
T1 - Oxidative damage in brain from human mutant APP/PS-1 double knock-in mice as a function of age{star, open}[1]This manuscript is dedicated to the life of Earl R. Stadtman (1919-2008), a dear friend who gave such elegant understanding of protein oxidation to the scientific community.
AU - Abdul, Hafiz Mohmmad
AU - Sultana, Rukhsana
AU - St. Clair, Daret K.
AU - Markesbery, William R.
AU - Butterfield, D. Allan
N1 - Funding Information:
This research was supported in part by NIH Grants AG-10836 and AG-029839 to D.A.B. and AG-05119 to D.A.B., D.S.C., and W.R.M. We thank Cephalon, Inc., Frazer, PA, for the donation of the animals used in this study.
PY - 2008/11/15
Y1 - 2008/11/15
N2 - Oxidative stress is strongly implicated in the progressive decline of cognition associated with aging and neurodegenerative disorders. In the brain, free radical-mediated oxidative stress plays a critical role in the age-related decline of cellular function as a result of the oxidation of proteins, lipids, and nucleic acids. A number of studies indicate that an increase in protein oxidation and lipid peroxidation is associated with age-related neurodegenerative diseases and cellular dysfunction observed in aging brains. Oxidative stress is one of the important factors contributing to Alzheimer's disease (AD), one of whose major hallmarks includes brain depositions of amyloid beta-peptide (Aβ) derived from amyloid precursor protein (APP). Mutation in APP and PS-1 genes, which increases production of the highly amyloidogenic amyloid β-peptide (Aβ42), is the major cause of familial AD. In the present study, protein oxidation and lipid peroxidation in the brain from knock-in mice expressing human mutant APP and PS-1 were compared with brain from wild type, as a function of age. The results suggest that there is an increased oxidative stress in the brain of wild-type mice as a function of age. In APP/PS-1 mouse brain, there is a basal increase (at 1 month) in oxidative stress compared to the wild type (1 month), as measured by protein oxidation and lipid peroxidation. In addition, age-related elevation of oxidative damage was observed in APP/PS-1 mice brain compared to that of wild-type mice brain. These results are discussed with reference to the importance of Aβ42-associated oxidative stress in the pathogenesis of AD.
AB - Oxidative stress is strongly implicated in the progressive decline of cognition associated with aging and neurodegenerative disorders. In the brain, free radical-mediated oxidative stress plays a critical role in the age-related decline of cellular function as a result of the oxidation of proteins, lipids, and nucleic acids. A number of studies indicate that an increase in protein oxidation and lipid peroxidation is associated with age-related neurodegenerative diseases and cellular dysfunction observed in aging brains. Oxidative stress is one of the important factors contributing to Alzheimer's disease (AD), one of whose major hallmarks includes brain depositions of amyloid beta-peptide (Aβ) derived from amyloid precursor protein (APP). Mutation in APP and PS-1 genes, which increases production of the highly amyloidogenic amyloid β-peptide (Aβ42), is the major cause of familial AD. In the present study, protein oxidation and lipid peroxidation in the brain from knock-in mice expressing human mutant APP and PS-1 were compared with brain from wild type, as a function of age. The results suggest that there is an increased oxidative stress in the brain of wild-type mice as a function of age. In APP/PS-1 mouse brain, there is a basal increase (at 1 month) in oxidative stress compared to the wild type (1 month), as measured by protein oxidation and lipid peroxidation. In addition, age-related elevation of oxidative damage was observed in APP/PS-1 mice brain compared to that of wild-type mice brain. These results are discussed with reference to the importance of Aβ42-associated oxidative stress in the pathogenesis of AD.
KW - APP/PS-1 human double mutant knock-in mouse
KW - Aging
KW - Alzheimer's disease
KW - Oxidative stress
UR - http://www.scopus.com/inward/record.url?scp=54349104874&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=54349104874&partnerID=8YFLogxK
U2 - 10.1016/j.freeradbiomed.2008.08.012
DO - 10.1016/j.freeradbiomed.2008.08.012
M3 - Article
C2 - 18762245
AN - SCOPUS:54349104874
SN - 0891-5849
VL - 45
SP - 1420
EP - 1425
JO - Free Radical Biology and Medicine
JF - Free Radical Biology and Medicine
IS - 10
ER -