Evidence map›Paper›PMID 23055486›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2012

Pituitary adenylate cyclase-activating polypeptide induces postsynaptically expressed potentiation in the intra-amygdala circuit.

Jun-Hyeong Cho, Ko Zushida, Gleb P Shumyatsky, William A Carlezon, Edward G Meloni, Vadim Y Bolshakov

Abstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

46 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. Circulating PACAP levels are associated with increased amygdala-default mode network resting-state connectivity in posttraumatic stress disorder.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2023
    Article
  14. Article
  15. Article
  16. Review
  17. Review
  18. Article
  19. Article
  20. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Jun-Hyeong ChoDepartment of Psychiatry, McLean Hospital, Harvard Medical School, Belmont, Massachusetts 02478, USA.
Ko Zushida
Gleb P Shumyatsky
William A Carlezon
Edward G Meloni
Vadim Y Bolshakov

Funding

Synaptic mechanisms in extinction of conditioned fearR01MH090464 · NIMH · MCLEAN HOSPITAL · PI BOLSHAKOV, VADIM · 2010 to 2014
$1.9M
PACAP signaling in stress and anxietyR01MH097860 · NIMH · MCLEAN HOSPITAL · PI CARLEZON, WILLIAM A. · 2013 to 2016
$1.6M
The role of GRP and GRPergic circuitry in fear memoryR01MH080328 · NIMH · RUTGERS, THE STATE UNIV OF N.J. · PI SHUMYATSKY, GLEB P · 2009 to 2010
$1.2M
PACAP signaling in stress and anxietyR56MH097860 · NIMH · MCLEAN HOSPITAL · PI CARLEZON, WILLIAM A. · 2012 to 2012
$381k
NIMH NIH HHS MH080328NIMH NIH HHS MH090464NIMH NIH HHS MH097860NIMH NIH HHS R01 MH080328NIMH NIH HHS R01 MH090464NIMH NIH HHS R01 MH097860NIMH NIH HHS R56 MH097860
6 · The paper itself

Abstract

Pituitary adenylate cyclase-activating polypeptide (PACAP) is a pleiotropic neuropeptide expressed in the brain, where it may act as a neuromodulator or neurotransmitter contributing to different behavioral processes and stress responses. PACAP is highly expressed in the amygdala, a subcortical brain area involved in both innate and learned fear, suggesting a role for PACAP-mediated signaling in fear-related behaviors. It remains unknown, however, whether and how PACAP affects neuronal and synaptic functions in the amygdala. In this study, we focused on neurons in the lateral division of the central nucleus (CeL), where PACAP-positive presynaptic terminals were predominantly found within the amygdala. In our experiments on rat brain slices, exogenous application of PACAP did not affect either resting membrane potential or membrane excitability of CeL neurons. PACAP enhanced, however, excitatory synaptic transmission in projections from the basolateral nucleus (BLA) to the CeL, while inhibitory transmission in the same pathway was unaffected. PACAP-induced potentiation of glutamatergic synaptic responses persisted after the washout of PACAP and was blocked by the VPAC1 receptor antagonist, suggesting that VPAC1 receptors might mediate synaptic effects of PACAP in the CeL. Moreover, potentiation of synaptic transmission by PACAP was dependent on postsynaptic activation of protein kinase A and calcium/calmodulin-dependent protein kinase II, as well as synaptic targeting of GluR1 subunit-containing AMPA receptors. Thus, PACAP may upregulate excitatory neurotransmission in the BLA-CeL pathway postsynaptically, consistent with the known roles of PACAP in control of fear-related behaviors.

Indexed as

Gene Expression RegulationAmygdalaAnimalsExcitatory Postsynaptic PotentialsFemaleMaleNerve NetPituitary Adenylate Cyclase-Activating PolypeptideRatsRats, Sprague-DawleyPituitary Adenylate Cyclase-Activating Polypeptide

Identifiers

PMID23055486
PMCPMC3490216

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.