» Articles » PMID: 36115597

The Central Extended Amygdala Guides Survival-relevant Tradeoffs: Implications for Understanding Common Psychiatric Disorders

Overview
Date 2022 Sep 17
PMID 36115597
Authors
Affiliations
Soon will be listed here.
Abstract

To thrive in challenging environments, individuals must pursue rewards while avoiding threats. Extensive studies in animals and humans have identified the central extended amygdala (EAc)-which includes the central nucleus of the amygdala (Ce) and bed nucleus of the stria terminalis (BST)-as a conserved substrate for defensive behavior. These studies suggest the EAc influences defensive responding and assembles fearful and anxious states. This has led to the proliferation of a view that the EAc is fundamentally a defensive substrate. Yet mechanistic work in animals has implicated the EAc in numerous appetitive and consummatory processes, yielding fresh insights into the microcircuitry of survival- and emotion-relevant response selection. Coupled with the EAc's centrality in a conserved network of brain regions that encode multisensory environmental and interoceptive information, these findings suggest a broader role for the EAc as an arbiter of survival- and emotion-relevant tradeoffs for action selection. Determining how the EAc optimizes these tradeoffs promises to improve our understanding of common psychiatric illnesses such as anxiety, depression, alcohol- and substance-use disorders, and anhedonia.

Citing Articles

An Honest Reckoning With the Amygdala and Mental Illness.

Fox A, Shackman A Am J Psychiatry. 2024; 181(12):1059-1075.

PMID: 39616453 PMC: 11611071. DOI: 10.1176/appi.ajp.20240941.


Temporal Dynamics of Uncertainty Cause Anxiety and Avoidance.

Holley D, Varga E, Boorman E, Fox A Comput Psychiatr. 2024; 8(1):85-91.

PMID: 38911145 PMC: 11192096. DOI: 10.5334/cpsy.105.


Rhesus infant nervous temperament predicts peri-adolescent central amygdala metabolism & behavioral inhibition measured by a machine-learning approach.

Holley D, Campos L, Drzewiecki C, Zhang Y, Capitanio J, Fox A Transl Psychiatry. 2024; 14(1):148.

PMID: 38490997 PMC: 10943234. DOI: 10.1038/s41398-024-02858-3.


Differential functional organization of amygdala-medial prefrontal cortex networks in macaque and human.

Giacometti C, Autran-Clavagnier D, Dureux A, Vinales L, Lamberton F, Procyk E Commun Biol. 2024; 7(1):269.

PMID: 38443489 PMC: 10914752. DOI: 10.1038/s42003-024-05918-y.


Acute and chronic alcohol modulation of extended amygdala calcium dynamics.

Roland A, Chao T, Hon O, Machinski S, Sides T, Lee S bioRxiv. 2023; .

PMID: 37873188 PMC: 10592781. DOI: 10.1101/2023.10.10.561741.


References
1.
Chen T, Wardill T, Sun Y, Pulver S, Renninger S, Baohan A . Ultrasensitive fluorescent proteins for imaging neuronal activity. Nature. 2013; 499(7458):295-300. PMC: 3777791. DOI: 10.1038/nature12354. View

2.
Mokdad A, Ballestros K, Echko M, Glenn S, Olsen H, Mullany E . The State of US Health, 1990-2016: Burden of Diseases, Injuries, and Risk Factors Among US States. JAMA. 2018; 319(14):1444-1472. PMC: 5933332. DOI: 10.1001/jama.2018.0158. View

3.
Baumgartner H, Schulkin J, Berridge K . Activating Corticotropin-Releasing Factor Systems in the Nucleus Accumbens, Amygdala, and Bed Nucleus of Stria Terminalis: Incentive Motivation or Aversive Motivation?. Biol Psychiatry. 2021; 89(12):1162-1175. PMC: 8178165. DOI: 10.1016/j.biopsych.2021.01.007. View

4.
Chang L, Gianaros P, Manuck S, Krishnan A, Wager T . A Sensitive and Specific Neural Signature for Picture-Induced Negative Affect. PLoS Biol. 2015; 13(6):e1002180. PMC: 4476709. DOI: 10.1371/journal.pbio.1002180. View

5.
Woo C, Chang L, Lindquist M, Wager T . Building better biomarkers: brain models in translational neuroimaging. Nat Neurosci. 2017; 20(3):365-377. PMC: 5988350. DOI: 10.1038/nn.4478. View