Thalamo-Basal Ganglia Connectivity in Postmenopausal Women Receiving Estrogen Therapy |
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Authors: | Heather?A.?Kenna,Natalie?L.?Rasgon mailto:nrasgon@stanford.edu" title=" nrasgon@stanford.edu" itemprop=" email" data-track=" click" data-track-action=" Email author" data-track-label=" " >Email author,Cheri?Geist,Gary?Small,Daniel?Silverman |
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Affiliation: | (1) Department of Psychiatry and Behavioral Sciences, Stanford Center for Neuroscience in Women’s Health, Stanford University School of Medicine, 401 Quarry Road, Stanford, CA, USA;(2) Department of Molecular and Medical Pharmacology, University of California, Los Angeles, CA, USA;(3) UCLA Center on Aging, Memory & Aging Research Center, Jane & Terry Semel Institute for Neuroscience & Human Behavior, University of California, Los Angeles, CA, USA |
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Abstract: | ![]() Cumulative data on the effects of estrogen therapy (ET) on brain function in postmenopausal women suggests that ET influences cerebral metabolism and may protect against age-related declines in various domains of cognitive function. The beneficial cognitive effects of ET may relate to its modulation of the thalamic-striatum cholinergic and dopaminergic systems, as the activity of both neurotransmitter systems in the thalamus appears to be positively influenced by estrogen. In the current study, we attempted to evaluated regional cerebral brain metabolism utilizing [18F]-fluorodeoxyglucose positron emission tomography in 11 healthy recently-postmenopausal women on ET (ET+) in comparison to 11 recently-postmenopausal and ET-naïve women (ET?) in order to assess the effects of ET on cholinergic and dopaminergic system regulation. Results showed thalamo-basal ganglia connectivity among ET+ women but not among ET? women. The presence of connectivity in the thalamo-striatal pathway in recently postmenopausal women suggests estrogen effects in preserving integrity of the cholinergic and dopaminergic systems. The results also suggest that ET initiated at or near the menopausal transition may modulate brain aging by mediating complex sensory-motor functions. |
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Keywords: | Estrogen Connectivity Brain Menopause Cholinergic Dopaminergic |
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