Evidence map›Paper›PMID 33767614›Full record

ArticleFrontiers in behavioral neuroscience2021

High-Frequency Stimulation of Ventral CA1 Neurons Reduces Amygdala Activity and Inhibits Fear.

Jalina Graham, Alexa F D'Ambra, Se Jung Jung, Yusuke Teratani-Ota, Nina Vishwakarma, Rasika Venkatesh, Abhijna Parigi, Evan G Antzoulatos, Diasynou Fioravante, Brian J Wiltgen

Open access · goldAbstract read
In one paragraph

Article in Frontiers in behavioral neuroscience, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
3.3field-weighted citation impact, top 7% of its field
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

15 citing papers in PubMed, 36 citations in OpenAlex.

  1. Integration of fear learning and fear expression across the dorsoventral axis of the hippocampus.Proceedings of the National Academy of Sciences of the United States of America · 2026
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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

10 authors at 1 institution in 1 country.

Jalina GrahamCenter for Neuroscience, University of California, Davis, Davis, CA, United States.
Alexa F D'AmbraCenter for Neuroscience, University of California, Davis, Davis, CA, United States.
Se Jung JungCenter for Neuroscience, University of California, Davis, Davis, CA, United States.
Yusuke Teratani-OtaCenter for Neuroscience, University of California, Davis, Davis, CA, United States.
Nina VishwakarmaDepartment of Neurobiology, Physiology and Behavior, University of California, Davis, Davis, CA, United States.
Rasika VenkateshDepartment of Plant Sciences, University of California, Davis, Davis, CA, United States.
Abhijna ParigiCenter for Neuroscience, University of California, Davis, Davis, CA, United States.
Evan G AntzoulatosCenter for Neuroscience, University of California, Davis, Davis, CA, United States.
Diasynou FioravanteCenter for Neuroscience, University of California, Davis, Davis, CA, United States.
Brian J WiltgenCenter for Neuroscience, University of California, Davis, Davis, CA, United States.
University of California, Davis · US

Funding

UC Davis MCB T32 Administrative Supplement to Recognize Excellence in Diversity, Equity, Inclusion, and Accessibility (DEIA) MentorshipT32GM007377 · NIGMS · UNIVERSITY OF CALIFORNIA DAVIS · PI CHEDIN, FREDERIC LOUIS · 1985 to 2023
$9.9M
Learning, Memory, and Plasticity (LaMP) Training ProgramT32MH112507 · NIMH · UNIVERSITY OF CALIFORNIA AT DAVIS · PI Karen Zito · 2017 to 2026
$2.4M
Neurobiological Mechanisms of Systems ConsolidationR01NS088053 · NINDS · UNIVERSITY OF CALIFORNIA AT DAVIS · PI WILTGEN, BRIAN J · 2015 to 2019
$1.7M
Tools for Dissecting Proximal and Distal CA1 Contributions to Learning and MemoryR21NS101694 · NINDS · UNIVERSITY OF CALIFORNIA AT DAVIS · PI WILTGEN, BRIAN J · 2017 to 2018
$409k
Investigation of cerebellar-amygdala connectivityR21MH114178 · NIMH · UNIVERSITY OF CALIFORNIA AT DAVIS · PI FIORAVANTE, DIASYNOU · 2017 to 2018
$393k
NIGMS NIH HHS T32 GM007377NIMH NIH HHS R21 MH114178NIMH NIH HHS T32 MH112507NINDS NIH HHS R01 NS088053NINDS NIH HHS R21 NS101694
6 · The paper itself

Abstract

The hippocampus can be divided into distinct segments that make unique contributions to learning and memory. The dorsal segment supports cognitive processes like spatial learning and navigation while the ventral hippocampus regulates emotional behaviors related to fear, anxiety and reward. In the current study, we determined how pyramidal cells in ventral CA1 respond to spatial cues and aversive stimulation during a context fear conditioning task. We also examined the effects of high and low frequency stimulation of these neurons on defensive behavior. Similar to previous work in the dorsal hippocampus, we found that cells in ventral CA1 expressed high-levels of c-Fos in response to a novel spatial environment. Surprisingly, however, the number of activated neurons did not increase when the environment was paired with footshock. This was true even in the subpopulation of ventral CA1 pyramidal cells that send direct projections to the amygdala. When these cells were stimulated at high-frequencies (20 Hz) we observed feedforward inhibition of basal amygdala neurons and impaired expression of context fear. In contrast, low-frequency stimulation (4 Hz) did not inhibit principal cells in the basal amygdala and produced an increase in fear generalization. Similar results have been reported in dorsal CA1. Therefore, despite clear differences between the dorsal and ventral hippocampus, CA1 neurons in each segment appear to make similar contributions to context fear conditioning.

Indexed as

context fearhippocampuslearningmemorymiceoptogenetics

Identifiers

PMID33767614
PMCPMC7985556
OpenAlexW3134749152

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.