TY - JOUR
T1 - Estrogen-induced plasticity from cells to circuits
T2 - predictions for cognitive function
AU - Brinton, Roberta Diaz
N1 - Funding Information:
The contributions of the Brinton laboratory estrogen research team, especially Jon Nilsen, Ronald Irwin, Shuhua Chen, Liqin Zhao, Ryan Hamilton and Jia Yao, and the graphic design by Kathy Cho are very gratefully acknowledged. I am indebted to the many important contributions generated by scientists working in the field and regret that much of the primary work could not be referenced owing to space limitations. Research and preparation of this review were supported by grants from the National Institute on Aging ( www.nia.nih.gov ; P01 AG026572; P01-AG014751; Project 2), National Institute of Mental Health ( www.nimh.nih.gov ; 1R01 MH67159), Kenneth T. and Eileen L. Norris Foundation ( www.ktn.org ) and Bensussen Translational Research Fund to R.D.B.
PY - 2009/4
Y1 - 2009/4
N2 - Controversy regarding estrogen action in the brain remains at the forefront of basic, translational and clinical science for women's health. Here, I provide an integrative analysis of estrogen-inducible plasticity and posit it as a strategy for predicting cognitive domains affected by estrogen in addition to sources of variability. Estrogen enhancement of plasticity is evidenced by increases in neurogenesis, neural network connectivity and synaptic transmission. In parallel, estrogen increases glucose transport, aerobic glycolysis and mitochondrial function to provide the ATP necessary to sustain increased energetic demand. The pattern of plasticity predicts that estrogen would preferentially affect cognitive tasks of greater complexity, temporal demand and associative challenge. Thus, estrogen deprivation should be associated with decrements in these functions. Estrogen regulation of plasticity and bioenergetics provides a framework for predicting estrogen-dependent cognitive functions while also identifying sources of variability and potential biomarkers for identifying women appropriate for hormone therapy.
AB - Controversy regarding estrogen action in the brain remains at the forefront of basic, translational and clinical science for women's health. Here, I provide an integrative analysis of estrogen-inducible plasticity and posit it as a strategy for predicting cognitive domains affected by estrogen in addition to sources of variability. Estrogen enhancement of plasticity is evidenced by increases in neurogenesis, neural network connectivity and synaptic transmission. In parallel, estrogen increases glucose transport, aerobic glycolysis and mitochondrial function to provide the ATP necessary to sustain increased energetic demand. The pattern of plasticity predicts that estrogen would preferentially affect cognitive tasks of greater complexity, temporal demand and associative challenge. Thus, estrogen deprivation should be associated with decrements in these functions. Estrogen regulation of plasticity and bioenergetics provides a framework for predicting estrogen-dependent cognitive functions while also identifying sources of variability and potential biomarkers for identifying women appropriate for hormone therapy.
UR - http://www.scopus.com/inward/record.url?scp=62949120140&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=62949120140&partnerID=8YFLogxK
U2 - 10.1016/j.tips.2008.12.006
DO - 10.1016/j.tips.2008.12.006
M3 - Review article
C2 - 19299024
AN - SCOPUS:62949120140
SN - 0165-6147
VL - 30
SP - 212
EP - 222
JO - Trends in Pharmacological Sciences
JF - Trends in Pharmacological Sciences
IS - 4
ER -