Go to JCI Insight
  • About
  • Editors
  • Consulting Editors
  • For authors
  • Publication ethics
  • Publication alerts by email
  • Advertising
  • Job board
  • Contact
  • Clinical Research and Public Health
  • Current issue
  • Past issues
  • By specialty
    • COVID-19
    • Cardiology
    • Gastroenterology
    • Immunology
    • Metabolism
    • Nephrology
    • Neuroscience
    • Oncology
    • Pulmonology
    • Vascular biology
    • All ...
  • Videos
    • ASCI Milestone Awards
    • Video Abstracts
    • Conversations with Giants in Medicine
  • Reviews
    • View all reviews ...
    • Neurodegeneration (Mar 2026)
    • Clinical innovation and scientific progress in GLP-1 medicine (Nov 2025)
    • Pancreatic Cancer (Jul 2025)
    • Complement Biology and Therapeutics (May 2025)
    • Evolving insights into MASLD and MASH pathogenesis and treatment (Apr 2025)
    • Microbiome in Health and Disease (Feb 2025)
    • Substance Use Disorders (Oct 2024)
    • View all review series ...
  • Viewpoint
  • Collections
    • In-Press Preview
    • Clinical Research and Public Health
    • Research Letters
    • Letters to the Editor
    • Editorials
    • Commentaries
    • Editor's notes
    • Reviews
    • Viewpoints
    • 100th anniversary
    • Top read articles

  • Current issue
  • Past issues
  • Specialties
  • Reviews
  • Review series
  • ASCI Milestone Awards
  • Video Abstracts
  • Conversations with Giants in Medicine
  • In-Press Preview
  • Clinical Research and Public Health
  • Research Letters
  • Letters to the Editor
  • Editorials
  • Commentaries
  • Editor's notes
  • Reviews
  • Viewpoints
  • 100th anniversary
  • Top read articles
  • About
  • Editors
  • Consulting Editors
  • For authors
  • Publication ethics
  • Publication alerts by email
  • Advertising
  • Job board
  • Contact
A noncanonical parasubthalamic nucleus–to–extended amygdala circuit converts chronic social stress into anxiety
Na Liu, Jun Wang, Huan Wang, Bin Gao, Zheng Lin, Tian-Le Xu, Shumin Duan, Han Xu
Na Liu, Jun Wang, Huan Wang, Bin Gao, Zheng Lin, Tian-Le Xu, Shumin Duan, Han Xu
View: Text | PDF
Research Article Cell biology Neuroscience

A noncanonical parasubthalamic nucleus–to–extended amygdala circuit converts chronic social stress into anxiety

  • Text
  • PDF
Abstract

Anxiety disorders pose a substantial threat to global mental health, with chronic stress identified as a major etiologic factor. Over the past few decades, extensive studies have revealed that chronic stress induces anxiety states through a distributed neuronal network of interconnected brain structures. However, the precise circuit mechanisms underlying the transition from chronic stress to anxiety remain incompletely understood. Employing the chronic social defeat stress (CSDS) paradigm in mice, we uncovered a critical role of the parasubthalamic nucleus (PSTh) in both the induction and expression of anxiety-like behavior. The anxiogenic effect was mediated by an excitatory trisynaptic circuitry involving the lateral parabrachial nucleus (LPB), PSTh, and bed nucleus of the stria terminalis (BNST). Furthermore, CSDS downregulated Kv4.3 channels in glutamatergic neurons of the PSTh. Reexpression of these channels dampened neuronal overexcitability and alleviated anxiety-like behavior in stressed animals. In parallel with the well-known anxiety network centered on the amygdala, here we identify a noncanonical LPB-PSTh-BNST pathway in the transformation of stress into anxiety. These findings suggest that the PSTh may serve as a potential therapeutic target for anxiety-related disorders.

Authors

Na Liu, Jun Wang, Huan Wang, Bin Gao, Zheng Lin, Tian-Le Xu, Shumin Duan, Han Xu

×

Figure 4

CSDS enhances the intrinsic excitability and excitatory synaptic inputs of PSTh glutamatergic neurons.

Options: View larger image (or click on image) Download as PowerPoint
CSDS enhances the intrinsic excitability and excitatory synaptic inputs ...
(A and B) Experimental timeline (A) and schematic diagram (B) of whole-cell patch-clamp recordings of PSThVglut2 neurons after CSDS. (C) Comparison of resting membrane potentials between 2 groups. n = 27 cells from 5 mice for control, and n = 27 cells from 7 mice for CSDS. (D and F) Representative traces of different current injections. (E and G) Statistical comparison of the membrane resistance (E) and rheobase (G) of PSTh glutamatergic neurons between control and CSDS groups. n = 15 cells from 5 mice for control, and n = 11 cells from 7 mice for CSDS. (H) Representative traces of 140 pA (left) and 240 pA (right) current injections. (I) Number of action potentials in response to incremental current injections. (J) Representative recorded samples of PSThVglut2 neuronal sEPSCs. (K and M) Cumulative probability of interevent interval (K) and amplitude (M) of sEPSCs. (L and N) Comparison of sEPSC frequency (L) and amplitude (N) between 2 groups. n = 38 cells from 6 mice for control, and n =21 cells from 5 mice for CSDS. Data are shown as the mean ± SEM. *P < 0.05 and ****P < 0.0001; 2-tailed unpaired t test in C, E, G, L, and N; 2-way ANOVA, Bonferroni’s multiple-comparison post hoc tests in I, K, and M.

Copyright © 2026 American Society for Clinical Investigation
ISSN: 0021-9738 (print), 1558-8238 (online)

Sign up for email alerts