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Time-Dependent Changes in Rat Brain Neuroactive Steroid Concentrations and GABA A Receptor Function after Acute Stress
Abstract
The time courses of changes in rat brain neuroactive steroid concentrations and gamma-aminobutyric acid type A (GABAA) receptor function elicited by acute stress were investigated in animals exposed to CO2 for 1 min, a treatment known to induce stress in rats and panic attacks in humans. Inhalation of CO2 induced increases in cerebral cortical steroid concentrations, the time dependence of which varied with the steroid examined. Thus, progesterone and deoxycorticosterone showed maximal increases (10- and 4-fold, respectively) 10 min after CO2 inhalation and had returned to basal values by 30 and 60 min, respectively. In contrast, pregnenolone and 3alpha-hydroxy-5alpha-pregnan-20-one (allopregnanolone) concentrations showed maximal increases (+174 and + 200%, respectively) at 30 min, were still higher than control at 60 min and returned to control values 120 min after stress. Inhalation of CO2 also resulted in increases in plasma steroid concentrations, most of which peaked at 30 min and had returned to control values by 60 min. A parallel analysis of the stress-induced changes in GABAA receptor function, assessed either biochemically by t-[35S]butylbicyclophosphorothionate ([35S]TBPS) binding to cerebral cortical membranes or behaviorally by the punished responding score in Vogel's test, showed that the effects of CO2 inhalation on both parameters were maximal (+51 and -40%, respectively) after 10 min; the behavioral reaction returned to normal after 60 min, whereas [35S]TBPS binding had returned to control values 120 min after stress. The results show that: (a) the maximal increase in the brain concentrations of allopregnanolone, a potent and efficacious positive modulator of GABAA receptors, occurred at a time (30 min) when both conflict behavior and [35S]TBPS binding begun to decrease, and (b) both allopregnanolone concentrations and [35S]TBPS binding had returned to control values 120 min after CO2 inhalation. The data are thus consistent with a physiological role of neuroactive steroids in restoring GABAergic tone after stress.
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“Accordingly, the first global effect of acute stress is a rapid decrease of GABAergic transmission together with an increase of glutamate transmission in brain areas involved in cognitive functions, such as prefrontal cortex and hippocampus [66,67].”
From Fibromyalgia pathogenesis explained by a neuroendocrine multistable model (2024) · cites this paper as [66]
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Neurosteroids: Endogenous Role in the Human Brian and Therapeutic Potentials
Reddy, D. (2010) · Progress in Brain Research · doi:10.1016/b978-0-444-53630-3.00008-7 · Cited by 556
“Acute stressors such as swimming, foot shock or carbon dioxide exposure elicit an increase in allopregnanolone and THDOC concentrations in plasma and in brain (Barbaccia et al., 1996; 1997).”
BackgroundConcas, A., Mostallino, M. C., Porcu, P., Follesa, P., Barbaccia, M., Trabucchi, M., Purdy, R., Grisenti, P., & Biggio, G. (1998) · Proceedings of the National Academy of Sciences of the United States of America · doi:10.1073/pnas.95.22.13284 · Cited by 432
Self-citationCirculating Levels of Allopregnanolone in Humans: Gender, Age, and Endocrine Influences
Genazzani, A. R., Petraglia, F., Bernardi, F., Casarosa, E., Salvestroni, C., Tonetti, A., Nappi, R. E., Luisi, S. V., Palumbo, M. A., Purdy, R. H., et al. (1998) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jcem.83.6.4905 · Cited by 392
Self-citationSchumacher, M., Mattern, C., Ghoumari, A. M., Oudinet, J., Lière, P., Labombarda, F., Sitruk-Ware, R. L., Nicola, A. F. D., & Guennoun, R. (2013) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2013.09.004 · Cited by 368
VanDoren, M. J., Matthews, D. B., Janis, G. C., Grobin, A. C., Devaud, L. L., & Morrow, A. L. (2000) · Journal of Neuroscience · doi:10.1523/jneurosci.20-05-01982.2000 · Cited by 314
“3a,5a-THP is increased in brain in many stress paradigms (Purdy et al., 1991; Barbaccia et al., 1996; Barbaccia et al., 1997), as well as during naturally occurring hormonal fluctuations such as the estrus cycle (Ichikawa et al., 1974; Paul and Purdy, 1992; Finn and Gee, 1993) and pregnancy (Concas…”
Background
Metadata
- Authors
- Barbaccia, M. L., Roscetti, G., Trabucchi, M., Mostallino, M. C., Concas, A., Purdy, R. H., & Biggio, G.
- Affiliations
- University of Rome Tor Vergata (IT)
- University of Cagliari (IT)
- University of California San Diego (US)
- ORCID
- Venue
- Neuroendocrinology
- Publisher
- S. Karger AG
- Published
- 2008-04-09
- Volume
- 63
- Issue
- 2
- Pages
- 166-172
- ISSN
- 0028-3835 (ISSN-L)
- 1423-0194
- OpenAlex
- W2084243951
- Cited by
- 303
- References
- 0
- Citations by year
- 2025: 3 · 2024: 9 · 2023: 3 · 2022: 7 · 2021: 6 · 2020: 7 · 2019: 5 · 2018: 5 · 2017: 2 · 2016: 9 · 2015: 4 · 2014: 17 · 2013: 7 · 2012: 13
- FWCI
- 6.12
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Neuroendocrinology (publishedVersion)
- PubMed (publishedVersion)
- Cineca Institutional Research Information System (Tor Vergata University) (submittedVersion)
- Topics
- Life Sciences › Neuroscience › Behavioral Neuroscience › Stress Responses and Cortisol
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuropeptides and Animal Physiology
- Keywords
- neurosteroids, GABAA receptor, acute stress, CO2 inhalation, allopregnanolone, progesterone, deoxycorticosterone, pregnenolone, cerebral cortex, GABAergic tone, panic attacks, [35S]TBPS binding
- MeSH terms
- Animals, Brain Chemistry, Carbon Dioxide, Cerebral Cortex, Conflict, Psychological, Male, Receptors, GABA-A, Steroids, Stress, Psychological, Time Factors, Rats, Sprague-Dawley, Bridged Bicyclo Compounds, Heterocyclic, Rats
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