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Bruce S. McEwen

Researcher at Rockefeller University

Publications -  1168
Citations -  214913

Bruce S. McEwen is an academic researcher from Rockefeller University. The author has contributed to research in topics: Hippocampus & Hippocampal formation. The author has an hindex of 215, co-authored 1163 publications receiving 200638 citations. Previous affiliations of Bruce S. McEwen include Yale University & National Institutes of Health.

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Steroid hormones: effect on brain development and function.

TL;DR: Hormones secreted by the adrenals, gonads and thyroid play an important role in mediating how the environment shapes the structure and function of the brain during early development, adult life and senescence.
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Testosterone cannot activate an adult-like stress response in prepubertal male rats.

TL;DR: It is concluded that the HPA neuroendocrine axis is further shaped during pubertal development to allow for the emergence of a more tightly regulated stress response in adulthood.
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Mitochondrial functions modulate neuroendocrine, metabolic, inflammatory, and transcriptional responses to acute psychological stress

TL;DR: The role of mitochondrial energetics and redox balance as modulators of key pathophysiological perturbations previously linked to disease is demonstrated, establishing mitochondria as stress-response modulators, with implications for understanding the mechanisms of stress pathophysiology and mitochondrial diseases.
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Autoradiographic localization of estradiol-binding neurons in the rat hippocampal formation and entorhinal cortex.

TL;DR: Because there is no significant nuclear accumulation of [3H]-alpha-testosterone in either the entorhinal cortex or hippocampal formation, it appears that aromatase enzyme activity is not a major contributor to estrogen receptor occupancy in adult rats.
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Estrogen Stimulates Postsynaptic Density-95 Rapid Protein Synthesis via the Akt/Protein Kinase B Pathway

TL;DR: An essential role for Akt is demonstrated in estrogen-stimulated dendritic spine protein expression, for the first time a signal transduction pathway in PSD-95 expression is described, and a novel, molecular mechanism by which ovarian hormones might translationally regulate synaptogenesis via activating protein synthesis for dendrite function is delineated.