GABA-A receptor modulating steroids in acute and chronic stress; relevance for cognition and dementia?
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Univ Arizona, Coll Med, Dept Pharmacol, Ctr Innovat Brain SciIssue Date
2019-12-20Keywords
AllopregnanoloneDementia
GABA-A receptor modulating steroid antagonists
GABA-A receptor modulating steroids
Learning
Memory
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ELSEVIER SCIENCE INCCitation
Bengtsson, S., Bäckström, T., Brinton, R., Irwin, R., Johansson, M., Sjöstedt, J., & Wang, M. (2020). GABA-A receptor modulating steroids in acute and chronic stress; relevance for cognition and dementia?. Neurobiology Of Stress, 12, 100206. doi: 10.1016/j.ynstr.2019.100206Journal
NEUROBIOLOGY OF STRESSRights
Copyright © 2019 The Author(s). Published by Elsevier Inc. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/BY-NC-ND/4.0/).Collection Information
This item from the UA Faculty Publications collection is made available by the University of Arizona with support from the University of Arizona Libraries. If you have questions, please contact us at repository@u.library.arizona.edu.Abstract
Cognitive dysfunction, dementia and Alzheimer's disease (AD) are increasing as the population worldwide ages. Therapeutics for these conditions is an unmet need. This review focuses on the role of the positive GABA-A receptor modulating steroid allopregnanolone (APa), it's role in underlying mechanisms for impaired cognition and of AD, and to determine options for therapy of AD. On one hand, APa given intermittently promotes neurogenesis, decreases AD-related pathology and improves cognition. On the other, continuous exposure of APa impairs cognition and deteriorates AD pathology. The disparity between these two outcomes led our groups to analyze the mechanisms underlying the difference. We conclude that the effects of APa depend on administration pattern and that chronic slightly increased APa exposure is harmful to cognitive function and worsens AD pathology whereas single administrations with longer intervals improve cognition and decrease AD pathology. These collaborative assessments provide insights for the therapeutic development of APa and APa antagonists for AD and provide a model for cross laboratory collaborations aimed at generating translatable data for human clinical trials.Note
Open access journalISSN
2352-2895PubMed ID
31921942Version
Final published versionae974a485f413a2113503eed53cd6c53
10.1016/j.ynstr.2019.100206
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Except where otherwise noted, this item's license is described as Copyright © 2019 The Author(s). Published by Elsevier Inc. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/BY-NC-ND/4.0/).
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