TY - JOUR
T1 - The healthy cell bias of estrogen action
T2 - mitochondrial bioenergetics and neurological implications
AU - Brinton, Roberta Diaz
N1 - Funding Information:
The many contributions of the Brinton laboratory estrogen and mitochondria research team, especially Jon Nilsen, Ronald Irwin, Jia Yao, Shuhua Chen, Liqin Zhao and Ryan Hamilton are gratefully acknowledged. I also thank Enrique Cadenas for critique of this manuscript and helpful discussions. Graphic contributions by Kathy Cho, Syeda Ahmed and Karren Wong are gratefully acknowledged. Research from our laboratory and preparation of this review were supported by grants from the National Institute of Mental Health (1R01 MH67159), National Institute on Aging (P01 AG026572) and the Kenneth T. and Eileen L. Norris Foundation to R.D.B.
PY - 2008/10
Y1 - 2008/10
N2 - The 'healthy cell bias of estrogen action' hypothesis examines the role that regulating mitochondrial function and bioenergetics play in promoting neural health and the mechanistic crossroads that lead to divergent outcomes following estrogen exposure. Estrogen-induced signaling pathways in hippocampal and cortical neurons converge upon the mitochondria to enhance aerobic glycolysis coupled to the citric acid cycle, mitochondrial respiration and ATP generation. Convergence of estrogen-induced signaling onto mitochondria is also a point of vulnerability when activated in diseased neurons which exacerbates degeneration through increased load on dysregulated calcium homeostasis. As the continuum of neurological health progresses from healthy to unhealthy so too do the benefits of estrogen or hormone therapy. The healthy cell bias of estrogen action hypothesis provides a lens through which to assess disparities in outcomes across basic and clinical science and on which to predict outcomes of estrogen interventions for sustaining neurological health and preventing age-associated neurodegenerative diseases such as Alzheimer's.
AB - The 'healthy cell bias of estrogen action' hypothesis examines the role that regulating mitochondrial function and bioenergetics play in promoting neural health and the mechanistic crossroads that lead to divergent outcomes following estrogen exposure. Estrogen-induced signaling pathways in hippocampal and cortical neurons converge upon the mitochondria to enhance aerobic glycolysis coupled to the citric acid cycle, mitochondrial respiration and ATP generation. Convergence of estrogen-induced signaling onto mitochondria is also a point of vulnerability when activated in diseased neurons which exacerbates degeneration through increased load on dysregulated calcium homeostasis. As the continuum of neurological health progresses from healthy to unhealthy so too do the benefits of estrogen or hormone therapy. The healthy cell bias of estrogen action hypothesis provides a lens through which to assess disparities in outcomes across basic and clinical science and on which to predict outcomes of estrogen interventions for sustaining neurological health and preventing age-associated neurodegenerative diseases such as Alzheimer's.
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U2 - 10.1016/j.tins.2008.07.003
DO - 10.1016/j.tins.2008.07.003
M3 - Review article
C2 - 18774188
AN - SCOPUS:52049083656
SN - 0166-2236
VL - 31
SP - 529
EP - 537
JO - Trends in Neurosciences
JF - Trends in Neurosciences
IS - 10
ER -