TY - CHAP
T1 - Spontaneous vertebrate models of Alzheimer dementia
T2 - Selectively bred strains (SAM strains)
AU - Sowell, Renã A.
AU - Butterfield, D. Allan
PY - 2011
Y1 - 2011
N2 - The senescence-accelerated mouse (SAM) strains, consisting of nine SAM-prone (SAMP) mice strains and three SAM-resistant (SAMR) strains, have been used extensively as models for various age-related disorders. SAMP mice undergo accelerated aging while SAMR mice undergo normal aging processes. One of the most employed SAM strains is SAMP8, which has deficits in learning and memory. Coupled to age-dependent deposition of amyloid β-peptide, such deficits allow it to serve as a good model of dementia-related disorders such as Alzheimer's disease (AD). Many studies have characterized the behavioral, pathological, genetic, and protein abnormalities of SAMP8 mice. Interestingly, genes and proteins that undergo significant alterations in SAMP8 brains are related to the following functional categories: neuroprotection, signal transduction, immune response, energy metabolism, mitochondrion, protein folding and degradation, reactive oxygen species production, cytoskeleton and transport, lipid abnormalities, and cholinergic dysfunction. This chapter provides a summary of these findings with regard to better understanding of AD pathogenesis.
AB - The senescence-accelerated mouse (SAM) strains, consisting of nine SAM-prone (SAMP) mice strains and three SAM-resistant (SAMR) strains, have been used extensively as models for various age-related disorders. SAMP mice undergo accelerated aging while SAMR mice undergo normal aging processes. One of the most employed SAM strains is SAMP8, which has deficits in learning and memory. Coupled to age-dependent deposition of amyloid β-peptide, such deficits allow it to serve as a good model of dementia-related disorders such as Alzheimer's disease (AD). Many studies have characterized the behavioral, pathological, genetic, and protein abnormalities of SAMP8 mice. Interestingly, genes and proteins that undergo significant alterations in SAMP8 brains are related to the following functional categories: neuroprotection, signal transduction, immune response, energy metabolism, mitochondrion, protein folding and degradation, reactive oxygen species production, cytoskeleton and transport, lipid abnormalities, and cholinergic dysfunction. This chapter provides a summary of these findings with regard to better understanding of AD pathogenesis.
KW - Alzheimer's disease
KW - Dementia
KW - Murine models
KW - SAMP8
KW - Senescence-accelerated mouse strain (SAM)
UR - http://www.scopus.com/inward/record.url?scp=78650933944&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=78650933944&partnerID=8YFLogxK
U2 - 10.1007/978-1-60761-898-0_15
DO - 10.1007/978-1-60761-898-0_15
M3 - Chapter
AN - SCOPUS:78650933944
SN - 9781607618973
T3 - Neuromethods
SP - 271
EP - 293
BT - Animal Models of Dementia
A2 - Deyn, Peter Paul
A2 - Dam, Debby
ER -