» Articles » PMID: 30186100

Traumatic Stress Produces Distinct Activations of GABAergic and Glutamatergic Neurons in Amygdala

Overview
Journal Front Neurosci
Date 2018 Sep 7
PMID 30186100
Citations 17
Authors
Affiliations
Soon will be listed here.
Abstract

Posttraumatic stress disorder (PTSD) is an anxiety disorder characterized by intrusive recollections of a severe traumatic event and hyperarousal following exposure to the event. Human and animal studies have shown that the change of amygdala activity after traumatic stress may contribute to occurrences of some symptoms or behaviors of the patients or animals with PTSD. However, it is still unknown how the neuronal activation of different sub-regions in amygdala changes during the development of PTSD. In the present study, we used single prolonged stress (SPS) procedure to obtain the animal model of PTSD, and found that 1 day after SPS, there were normal anxiety behavior and extinction of fear memory in rats which were accompanied by a reduced proportion of activated glutamatergic neurons and increased proportion of activated GABAergic neurons in basolateral amygdala (BLA). About 10 days after SPS, we observed enhanced anxiety and impaired extinction of fear memory with increased activated both glutamatergic and GABAergic neurons in BLA and increased activated GABAergic neurons in central amygdala (CeA). These results indicate that during early and late phase after traumatic stress, distinct patterns of activation of glutamatergic neurons and GABAergic neurons are displayed in amygdala, which may be implicated in the development of PTSD.

Citing Articles

Effects of TrkB-related induced metaplasticity within the BLA on anxiety, extinction learning, and plasticity in BLA-modulated brain regions.

Hazra J, Shrivastava K, Wustner L, Anunu R, Chervinsky E, Hazra S Behav Brain Funct. 2025; 21(1):4.

PMID: 40033342 PMC: 11874401. DOI: 10.1186/s12993-025-00267-0.


Temporal-Posterior Alpha Power in Resting-State Electroencephalography as a Potential Marker of Complex Childhood Trauma in Institutionalized Adolescents.

Marcu G, Bacila C, Zagrean A Brain Sci. 2024; 14(6).

PMID: 38928584 PMC: 11201643. DOI: 10.3390/brainsci14060584.


The Relationship between Post-Traumatic Stress Disorder Due to Brain Injury and Glutamate Intake: A Systematic Review.

Gruenbaum B, Zlotnik A, Oleshko A, Matalon F, Shiyntum H, Frenkel A Nutrients. 2024; 16(6).

PMID: 38542812 PMC: 10975349. DOI: 10.3390/nu16060901.


Exploring gene-drug interactions for personalized treatment of post-traumatic stress disorder.

Skolariki K, Vlamos P Front Comput Neurosci. 2024; 17:1307523.

PMID: 38274128 PMC: 10808814. DOI: 10.3389/fncom.2023.1307523.


The Neuroendocrine Impact of Acute Stress on Synaptic Plasticity.

Dos-Santos R, Sweeten B, Stelly C, Tasker J Endocrinology. 2023; 164(11).

PMID: 37788632 PMC: 11046011. DOI: 10.1210/endocr/bqad149.


References
1.
Xiao B, Han F, Shi Y . Dysfunction of Ca2+/CaM kinase IIalpha cascades in the amygdala in post-traumatic stress disorder. Int J Mol Med. 2009; 24(6):795-9. DOI: 10.3892/ijmm_00000294. View

2.
McDonald A . Cortical pathways to the mammalian amygdala. Prog Neurobiol. 1998; 55(3):257-332. DOI: 10.1016/s0301-0082(98)00003-3. View

3.
Dickinson A, Jones M, Milne E . Measuring neural excitation and inhibition in autism: Different approaches, different findings and different interpretations. Brain Res. 2016; 1648(Pt A):277-289. DOI: 10.1016/j.brainres.2016.07.011. View

4.
Gonzales C, Kaufman D, Tobin A, Chesselet M . Distribution of glutamic acid decarboxylase (Mr 67,000) in the basal ganglia of the rat: an immunohistochemical study with a selective cDNA-generated polyclonal antibody. J Neurocytol. 1991; 20(12):953-61. DOI: 10.1007/BF01187913. View

5.
Corchs F, Nutt D, Hood S, Bernik M . Serotonin and sensitivity to trauma-related exposure in selective serotonin reuptake inhibitors-recovered posttraumatic stress disorder. Biol Psychiatry. 2009; 66(1):17-24. DOI: 10.1016/j.biopsych.2009.01.031. View