Chronic stress impairs GABAergic control of amygdala through suppressing the tonic GABAA receptor currents
Open accessAbstract
BACKGROUND: Chronic stress is generally known to exacerbate the development of numerous neuropsychiatric diseases such as fear and anxiety disorders, which is at least partially due to the disinhibition of amygdala subsequent to the prolonged stress exposure. GABA receptor A (GABAAR) mediates the primary component of inhibition in brain and its activation produces two forms of inhibition: the phasic and tonic inhibition. While both of them are critically engaged in limiting the activity of amygdala, their roles in the amygdala disinhibition subsequent to chronic stress exposure are largely unknown. RESULTS: We investigated the possible alterations of phasic and tonic GABAAR currents and their roles in the amygdala disinhibition subsequent to chronic stress. We found that both chronic immobilization and unpredictable stress led to long lasting loss of tonic GABAAR currents in the projection neurons of lateral amygdala. By contrast, the phasic GABAAR currents, as measured by the spontaneous inhibitory postsynaptic currents, were virtually unaltered. The loss of tonic inhibition varied with the duration of daily stress and the total days of stress exposure. It was prevented by pretreatment with metyrapone to block corticosterone synthesis or RU 38486, a glucocorticoid receptor antagonist, suggesting the critical involvement of glucocorticoid receptor activation. Moreover, chronic treatment with corticosterone mimicked the effect of chronic stress and reduced the tonic inhibition in lateral amygdala of control mice. The loss of tonic inhibition resulted in the impaired GABAergic gating on neuronal excitability in amygdala, which was prevented by metyrapone pretreatment. CONCLUSIONS: Our study suggests that enduring loss of tonic but not phasic GABAAR currents critically contributes to the prolonged amygdala disinhibition subsequent to chronic stress. We propose that the preferential loss of tonic inhibition may account for the development of stress-related neuropsychiatric diseases.
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The BLA is generally hyperactive following chronic stress.
“The stress-induced attenuation of BLA→DMS activity was surprising because the BLA is, generally, hyperactive following chronic stress54–61 (c.f.62).”
From A dual-pathway architecture for stress to disrupt agency and promote habit (2025) · cites this paper as [55]
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References 56 · Cited by 99
- Authors
- Liu, Z.-P., Song, C., Wang, M., He, Y., Xu, X.-B., Pan, H.-Q., Chen, W.-B., Peng, W.-J., & Pan, B.-X.
- Affiliations
- Nanchang University (CN)
- Corresponding author
- Pan, Bing-Xing
- Venue
- Molecular Brain
- Published
- 2014-04-24
- Volume
- 7
- Issue
- 1
- Pages
- 32-32
- ISSN
- 1756-6606 (ISSN-L)
- PMC
- PMC4012764
- OpenAlex
- W2105616924
- Cited by
- 99
- References
- 56
- Citations by year
- 2026: 10 · 2025: 9 · 2024: 9 · 2023: 4 · 2022: 2 · 2021: 9 · 2020: 10 · 2019: 8 · 2018: 8 · 2017: 15 · 2016: 8 · 2015: 6 · 2014: 1
- FWCI
- 4.57
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- cc-by
- Locations
- Molecular Brain (publishedVersion, cc-by)
- Europe PMC (PubMed Central) (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- Funders
- Major State Basic Research Development Program of China (2014CB846100)
- Program for New Century Excellent Talents in University
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Neuroscience › Behavioral Neuroscience › Stress Responses and Cortisol
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
- Keywords
- chronic stress, phasic inhibition, lateral amygdala, glucocorticoid receptor, corticosterone, metyrapone, mifepristone, restraint stress, unpredictable stress, spontaneous inhibitory postsynaptic currents, anxiety disorders, neuronal excitability
- MeSH terms
- Action Potentials, Amygdala, Animals, Chronic Disease, Corticosterone, gamma-Aminobutyric Acid, Immobilization, Inhibition, Psychological, Male, Mice, Inbred C57BL, Neurons, Receptors, GABA-A, Receptors, Glucocorticoid, Stress, Psychological, Ion Channel Gating, Mice, Inhibitory Postsynaptic Potentials
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