4.7 Article

Chronic Stress Induces Maladaptive Behaviors by Activating Corticotropin-Releasing Hormone Signaling in the Mouse Oval Bed Nucleus of the Stria Terminalis

期刊

JOURNAL OF NEUROSCIENCE
卷 40, 期 12, 页码 2519-2537

出版社

SOC NEUROSCIENCE
DOI: 10.1523/JNEUROSCI.2410-19.2020

关键词

anxiety; bed nucleus of stria terminalis; chronic stress; corticotropin releasing hormone

资金

  1. National Institute of Mental Health [R01 MH112861]
  2. NWO
  3. Alzheimer Nederland
  4. Urban Mental Health Program of the University of Amsterdam
  5. National Institutes of Health [R21 ES027119]
  6. NIAA [R01 AA023797]

向作者/读者索取更多资源

The bed nucleus of the stria terminalis (BNST) is a forebrain region highly responsive to stress that expresses corticotropin-releasing hormone (CRH) and is implicated in mood disorders, such as anxiety. However, the exact mechanism by which chronic stress induces CRH-mediated dysfunction in BNST and maladaptive behaviors remains unclear. Here, we first confirmed that selective acute optogenetic activation of the oval nucleus BNST (ovBNST) increases maladaptive avoidance behaviors in male mice. Next, we found that a 6 week chronic variable mild stress (CVMS) paradigm resulted in maladaptive behaviors and increased cellular excitability of ovBNST CRH neurons by potentiating mEPSC amplitude, altering the resting membrane potential, and diminishing M-currents (a voltage-gated K+ current that stabilizes membrane potential) in ex vivo slices. CVMS also increased c-fos(+) cells in ovBNST following handling. We next investigated potential molecular mechanism underlying the electrophysiological effects and observed that CVMS increased CRH(+ )and pituitary adenylate cyclase-activating polypeptide (PACAP; a CRH upstream regulator) cells but decreased striatal-enriched protein tyrosine phosphatase(+) (a STEP CRH inhibitor) cells in ovBNST. Interestingly, the electrophysiological effects of CVMS were reversed by CRHR1-selective antagonist R121919 application. CVMS also activated protein kinase A (PICA) in BNST, and chronic infusion of the PKA-selective antagonist H89 into ovBNST reversed the effects of CVMS. Coadministration of the PKA agonist forskolin prevented the beneficial effects of R121919. Finally, CVMS induced an increase in surface expression of phosphorylated GluR1 (S845) in BNST. Collectively, these findings highlight a novel and indispensable stress-induced role for PKA-dependent CRHRI signaling in activating BNST CRH neurons and mediating maladaptive behaviors.

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