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A glial switch for pain-driven anxiety
Hector E Yarur1, Sofia E Shirley2, Huikun Wang1
1Neuromodulation and Synaptic Integration Unit, National Institute of Mental Health Intramural Research Program, National Institutes of Health, Bethesda, MD, USA.
Neuron
|December 4, 2025
Summary
Glial cells in the brain's central amygdala (CeA) influence defensive behaviors. Dynorphin/kappa opioid receptor signaling in CeA astrocytes modulates anxiety during chronic pain.
Area of Science:
- Neuroscience
- Cell Biology
- Behavioral Science
Background:
- The central amygdala (CeA) is crucial for defensive behaviors.
- The roles of glial cells and stress neuromodulators in the CeA are not fully understood.
Purpose of the Study:
- To investigate the contribution of glial cells and neuromodulators in the CeA.
- To explore the function of dynorphin/kappa opioid receptor signaling in CeA astrocytes.
Main Methods:
- Utilized advanced techniques to study CeA astrocyte signaling.
- Investigated the impact of dynorphin/kappa opioid receptor pathways.
Main Results:
- Dynorphin/kappa opioid receptor signaling in CeA astrocytes was found to be active.
- This signaling pathway modulates anxiety-like behavior.
Conclusions:
- Astrocytes in the CeA play a significant role in defensive behavior modulation.
- Dynorphin/kappa opioid receptor signaling in CeA astrocytes is a key mechanism influencing anxiety during chronic pain.
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