Evidence map›Paper›PMID 39122815›Full record

ReviewNeuropsychopharmacology : official publication of the American College of Neuropsychopharmacology2024

Identifying dysfunctional cell types and circuits in animal models for psychiatric disorders with calcium imaging.

Mark M Gergues, Lahin K Lalani, Mazen A Kheirbek

Erratum issuedAbstract readReview
In one paragraph

Review in Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

3 authors.

Mark M GerguesNeuroscience Graduate Program, University of California San Francisco, San Francisco, CA, USA.
Lahin K LalaniNeuroscience Graduate Program, University of California San Francisco, San Francisco, CA, USA.
Mazen A KheirbekNeuroscience Graduate Program, University of California San Francisco, San Francisco, CA, USA. mazen.kheirbek@ucsf.edu.ORCID 0000-0001-9157-7363

Funding

Hippocampal modulation of subcortical circuits in the control of emotional behaviorR01MH108623 · NIMH · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI Mazen A Kheirbek · 2016 to 2026
$6.0M
Cell-type, circuit and network mechanisms of adult oligodendrogenesis in memory storage and retrievalR01MH125515 · NIMH · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI CHAN, JONAH R, KHEIRBEK, MAZEN A · 2021 to 2025
$3.4M
Circuit dynamics supporting associative learning in the dentate gyrusR01DC019813 · NIDCD · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI KHEIRBEK, MAZEN A · 2021 to 2025
$2.8M
Circuit and cellular mechanisms of adult neurogenesis in context encoding and discriminationR01MH111754 · NIMH · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI KHEIRBEK, MAZEN A · 2017 to 2021
$2.0M
Ventral hippocampal encoding of anxiety representations is shaped by thalamic input.F99NS130927 · NINDS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI GERGUES, MARK M · 2022 to 2023
$81k
Thalamic inputs modulate anxiety-related representations in the hippocampusF31MH130127 · NIMH · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI GERGUES, MARK M · 2022 to 2022
$20k
NIDCD NIH HHS R01 DC019813NIMH NIH HHS F31 MH130127NIMH NIH HHS R01 MH108623NIMH NIH HHS R01 MH111754NIMH NIH HHS R01 MH125515NINDS NIH HHS F99 NS130927U.S. Department of Health & Human Services | NIH | National Institute of Neurological Disorders and Stroke (NINDS) DSPAN F99/K00 NS130927
6 · The paper itself

Abstract

A central goal of neuroscience is to understand how the brain transforms external stimuli and internal bodily signals into patterns of activity that underlie cognition, emotional states, and behavior. Understanding how these patterns of activity may be disrupted in mental illness is crucial for developing novel therapeutics. It is well appreciated that psychiatric disorders are complex, circuit-based disorders that arise from dysfunctional activity patterns generated in discrete cell types and their connections. Recent advances in large-scale, cell-type specific calcium imaging approaches have shed new light on the cellular, circuit, and network-level dysfunction in animal models for psychiatric disorders. Here, we highlight a series of recent findings over the last ~10 years from in vivo calcium imaging studies that show how aberrant patterns of activity in discrete cell types and circuits may underlie behavioral deficits in animal models for several psychiatric disorders, including depression, anxiety, autism spectrum disorders, and schizophrenia. These advances in calcium imaging in pre-clinical models demonstrate the power of cell-type-specific imaging tools in understanding the underlying dysfunction in cell types, activity patterns, and neural circuits that may contribute to disease and provide new blueprints for developing more targeted therapeutics and treatment strategies.

Indexed as

CalciumDisease Models, AnimalMental DisordersAnimalsBrainHumansNeuronsCalcium

Identifiers

PMID39122815
PMCPMC11525937

What Socratic holds

Textmetadata
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 Socratic graph.