Cited by 66Neuroscience and Neuropharmacology ResearchNeurotransmitter Receptor Influence on BehaviorAnxiety, Depression, Psychometrics, Treatment, Cognitive Processes

Chronic inhibition of GABA synthesis in the bed nucleus of the stria terminalis elicits anxiety-like behavior

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Sajdyk, TJ, Johnson, PL, Fitz, SD, Shekhar, A.·2008·Journal of Psychopharmacology

Abstract

The current study tested the hypothesis that chronic loss of inhibitory GABAergic tone in the bed nucleus of the stria terminalis (BNST), a region implicated in anxiety behavior, results in generalized anxiety disorder-like behaviors without panic-like responses (i.e., tachycardia, hypertension and tachypnea) following panicogenic stimuli (e.g., sodium lactate infusions). To test this hypothesis, the GABA synthesis inhibitor L-allylglycine (L-AG) or its inactive isomer D-AG was chronically infused into the BNST of male rats via osmotic mini-pumps. L-AG, but not D-AG, treated rats had increased anxiety-like behavior as measured by social interaction (SI) and elevated-plus maze paradigms. Restoring GABAergic tone, with 100pmoles/100nl of muscimol (a GABA A receptor agonist), in the BNST of L-AG treated rats attenuated L-AG-induced anxiety-like behavior in the SI test. To assess panic-like states, L-AG treated rats were intravenously infused with 0.5 M sodium lactate, a panicogenic agent, prior to assessing SI and cardiorespiratory responses. L-AG decreased SI duration again; however, sodium lactate did not induce panic-like cardiorespiratory responses. These findings demonstrate that GABA inhibition in the BNST elicits anxiety-like behavior without increasing sensitivity to lactate, thus suggesting a behavioral profile similar to that of generalized anxiety-like behavior rather than that of panic.

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  • Inhibition of GABA synthesis in the bed nucleus of the stria terminalis produced an anxiogenic effect in the plus-maze and social interaction test, reversed by local infusion of muscimol in the bed nucleus of the stria terminalis.

    “Inhibition of GABA synthesis in the BNST produced an anxiogenic effect in the plus-maze and social interaction test, another measure of sustained fear in which rats exposed to novel places under high illumination tend not to interact with each other; this effect was reversed by local infusion of muscimol in the BNST (Sajdyk et al, 2008).”

    From Phasic vs Sustained Fear in Rats and Humans: Role of the Extended Amygdala in Fear vs Anxiety (2010) · cites this paper as Sajdyk et al, 2008

    The Elevated Plus-Maze, Social Interaction, and Discussion sections report anxiety-like effects after GABA-synthesis inhibition in the BNST; the Social Interaction results report reversal by local muscimol. However, the Social Interaction methods say testing occurred under low light in familiar conditions, not in novel places under high illumination. The paper describes the test as measuring anxiety-like behavior, not specifically sustained fear. (LLM, conf=0.90)

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  • Chronic inhibition of GABA synthesis in the bed nucleus of the stria terminalis produces anxiogenic effects that are reversible by local muscimol infusion into the bed nucleus of the stria terminalis.

    “Anxiogenic effects were also found after chronic inhibition of GABA synthesis in the BNST, and these effects were reversible by local infusion of muscimol into the BNST (Sajdyk et al, 2008).”

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References 67 · Cited by 66

Research works printed but not linked: 2

  1. Egli RE, Winder DG. Dorsal and ventral distribution of excitable and synaptic properties of neurons of the bed nucleus of the stria terminalis. J Neurophysiol. 2003; 90:405-414. [PubMed: 12649311]
  2. Shekhar, AKS.; Simon, JR.; McBride, WJ. Pharmacology Biochemistry & Behavior. Vol. 55. 1996. Dorsomedial Hypothalamic GABA Dysfunction Produces Physiological Arousal Following Sodium Lactate Infusions; p. 249-256.

Authors
Sajdyk, T., Johnson, P., Fitz, S., & Shekhar, A.
Affiliations
  • Departments of Psychiatry and Biochemistry, Indiana University School of Medicine, Indianapolis, IN 46202, USA
  • Department of Psychiatry, Indiana University School of Medicine, Indianapolis, IN 46202, USA
  • Indiana University Indianapolis (US)
Corresponding author
Shekhar, A.
Venue
Journal of Psychopharmacology
Published
2008-05-30
Volume
22
Issue
6
Pages
633-641
ISSN
  • 0269-8811 (ISSN-L)
  • 1461-7285
OpenAlex
W2013513295
Cited by
66
References
67
Citations by year
2026: 2 · 2025: 4 · 2024: 3 · 2023: 5 · 2022: 1 · 2021: 2 · 2020: 2 · 2019: 5 · 2018: 6 · 2017: 2 · 2016: 4 · 2015: 3 · 2014: 6 · 2013: 5 · 2012: 7
FWCI
1.15
Type
journal article
Language
en
Open access
Locations
  • Journal of Psychopharmacology (publishedVersion)
  • PubMed (publishedVersion)
  • PubMed Central (acceptedVersion)
  • IUScholarWorks (Indiana University) (submittedVersion)
Funders
  • National Institutes of Health (UL1TR001108)
  • National Institute of Mental Health (R01-MH52619, MH-65702, R01MH052619, R01MH065702, MH 52619)
  • National Center for Advancing Translational Sciences
Topics
  • Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
  • Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neurotransmitter Receptor Influence on Behavior
  • Social Sciences › Psychology › Experimental and Cognitive Psychology › Anxiety, Depression, Psychometrics, Treatment, Cognitive Processes
Keywords
bed nucleus of the stria terminalis, GABA synthesis inhibition, anxiety-like behavior, generalized anxiety disorder, panic, sodium lactate, muscimol, GABAergic tone, social interaction, elevated plus maze, cardiorespiratory responses
MeSH terms
Animals, Anxiety, Blood Pressure, gamma-Aminobutyric Acid, Heart Rate, Male, Septal Nuclei, Social Behavior, Rats, Sprague-Dawley, GABA Antagonists, Maze Learning, Sodium Lactate, Rats

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