Cited by 99Neuroscience and Neuropharmacology ResearchStress Responses and CortisolMemory and Neural Mechanisms

Chronic stress impairs GABAergic control of amygdala through suppressing the tonic GABAA receptor currents

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Liu, Zhi-Peng, Song, Chen, Wang, Min, He, Ye, Xu, Xiao-Bin, Pan, Han-Qing, Chen, Wen-Bing, Peng, Wei-Jie +1 more·2014·Molecular Brain

Abstract

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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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)
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
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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