TY - JOUR
T1 - Characterizing cognitive aging of working memory and executive function in animal models
AU - Bizon, Jennifer L.
AU - Foster, Thomas C.
AU - Alexander, Gene E.
AU - Glisky, Elizabeth L.
PY - 2012
Y1 - 2012
N2 - Executive functions supported by prefrontal cortical (PFC) systems provide essential control and planning mechanisms to guide goal-directed behavior. As such, age-related alterations in executive functions can mediate profound and widespread deficits on a diverse array of neurocognitive processes. Many of the critical neuroanatomical and functional characteristics of prefrontal cortex are preserved in rodents, allowing for meaningful cross species comparisons relevant to the study of cognitive aging. In particular, as rodents lend themselves to genetic, cellular and biochemical approaches, rodent models of executive function stand to significantly contribute to our understanding of the critical neurobiological mechanisms that mediate decline of executive processes across the lifespan. Moreover, rodent analogs of executive functions that decline in human aging represent an essential component of a targeted, rational approach for developing and testing effective treatment and prevention therapies for age-related cognitive decline. This paper reviews behavioral approaches used to study executive function in rodents, with a focus on those assays that share a foundation in the psychological and neuroanatomical constructs important for human aging. A particular emphasis is placed on behavioral approaches used to assess working memory and cognitive flexibility, which are sensitive to decline with age across species and for which strong rodent models currently exist. In addition, other approaches in rodent behavior that have potential for providing analogs to functions that reliably decline to human aging (e.g., information processing speed) are discussed.
AB - Executive functions supported by prefrontal cortical (PFC) systems provide essential control and planning mechanisms to guide goal-directed behavior. As such, age-related alterations in executive functions can mediate profound and widespread deficits on a diverse array of neurocognitive processes. Many of the critical neuroanatomical and functional characteristics of prefrontal cortex are preserved in rodents, allowing for meaningful cross species comparisons relevant to the study of cognitive aging. In particular, as rodents lend themselves to genetic, cellular and biochemical approaches, rodent models of executive function stand to significantly contribute to our understanding of the critical neurobiological mechanisms that mediate decline of executive processes across the lifespan. Moreover, rodent analogs of executive functions that decline in human aging represent an essential component of a targeted, rational approach for developing and testing effective treatment and prevention therapies for age-related cognitive decline. This paper reviews behavioral approaches used to study executive function in rodents, with a focus on those assays that share a foundation in the psychological and neuroanatomical constructs important for human aging. A particular emphasis is placed on behavioral approaches used to assess working memory and cognitive flexibility, which are sensitive to decline with age across species and for which strong rodent models currently exist. In addition, other approaches in rodent behavior that have potential for providing analogs to functions that reliably decline to human aging (e.g., information processing speed) are discussed.
KW - Aged
KW - Cognitive flexibility
KW - Delayed match-to-place
KW - Prefrontal cortex
KW - Rat
KW - Rodents
KW - Set-shifting
KW - Water maze
UR - http://www.scopus.com/inward/record.url?scp=84870495282&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84870495282&partnerID=8YFLogxK
U2 - 10.3389/fnagi.2012.00019
DO - 10.3389/fnagi.2012.00019
M3 - Article
C2 - 22988438
AN - SCOPUS:84870495282
SN - 1663-4365
VL - 4
JO - Frontiers in Aging Neuroscience
JF - Frontiers in Aging Neuroscience
IS - SEP
M1 - Article 19
ER -