β-Arrestin-dependent ERK signaling reduces anxiety-like and conditioned fear-related behaviors in mice
| Autor: | Mee Jung Ko, Terrance Chiang, Grace E. Mulia, Angel Lin, Arbaaz A. Mukadam, Anna M. Gutridge, Julia A. Chester, Richard M. van Rijn |
|---|---|
| Rok vydání: | 2021 |
| Předmět: |
0301 basic medicine
Agonist Male G protein medicine.drug_class Striatum Nucleus accumbens Anxiety Biochemistry Amygdala Article 03 medical and health sciences Mice 0302 clinical medicine medicine Arrestin Animals Molecular Biology beta-Arrestins G protein-coupled receptor Chemistry Kinase Cell Biology Fear beta-Arrestin 2 Mice Inbred C57BL 030104 developmental biology medicine.anatomical_structure beta-Arrestin 1 Neuroscience 030217 neurology & neurosurgery |
| Zdroj: | Sci Signal |
| ISSN: | 1937-9145 |
| Popis: | G protein–coupled receptors (GPCRs) are implicated in the regulation of fear and anxiety. GPCR signaling involves canonical G protein pathways but can also engage downstream kinases and effectors through scaffolding interactions mediated by β-arrestin. Here, we investigated whether β-arrestin signaling regulates anxiety-like and fear-related behavior in mice in response to activation of the GPCR δ-opioid receptor (δOR or DOR). Administration of β-arrestin–biased δOR agonists to male C57BL/6 mice revealed β-arrestin 2–dependent activation of extracellular signal–regulated kinases 1 and 2 (ERK1/2) in the dorsal hippocampus and amygdala and β-arrestin 1–dependent activation of ERK1/2 in the nucleus accumbens. In mice, β-arrestin–biased agonist treatment was associated with reduced anxiety-like and fear-related behaviors, with some overlapping and isoform-specific input. In contrast, applying a G protein–biased δOR agonist decreased ERK1/2 activity in all three regions as well as the dorsal striatum and was associated with increased fear-related behavior without effects on baseline anxiety. Our results indicate a complex picture of δOR neuromodulation in which β-arrestin 1– and 2–dependent ERK signaling in specific brain subregions suppresses behaviors associated with anxiety and fear and opposes the effects of G protein–biased signaling. Overall, our findings highlight the importance of noncanonical β-arrestin–dependent GPCR signaling in the regulation of these interrelated emotions. |
| Databáze: | OpenAIRE |
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