Evidence map›Paper›PMID 39314375›Full record

ArticlebioRxiv : the preprint server for biology2024

Behavioral state and stimulus strength regulate the role of somatostatin interneurons in stabilizing network activity.

Celine M Cammarata, Yingming Pei, Brenda C Shields, Shaun S X Lim, Tammy Hawley, Jennifer Y Li, David St Amand, Nicolas Brunel, Michael R Tadross, Lindsey L Glickfeld

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors.

Celine M CammarataDepartment of Neurobiology, Duke University Medical Center, Durham, NC 27710 USA.
Yingming PeiDepartment of Neurobiology, Duke University Medical Center, Durham, NC 27710 USA.
Brenda C ShieldsDepartment of Biomedical Engineering, Duke University, Durham, NC 27701 USA.
Shaun S X LimDepartment of Biomedical Engineering, Duke University, Durham, NC 27701 USA.
Tammy HawleyDepartment of Neurobiology, Duke University Medical Center, Durham, NC 27710 USA.
Jennifer Y LiDepartment of Neurobiology, Duke University Medical Center, Durham, NC 27710 USA.
David St AmandDepartment of Neurobiology, Duke University Medical Center, Durham, NC 27710 USA.
Nicolas BrunelDepartment of Neurobiology, Duke University Medical Center, Durham, NC 27710 USA.
Michael R TadrossDepartment of Biomedical Engineering, Duke University, Durham, NC 27701 USA.
Lindsey L GlickfeldDepartment of Neurobiology, Duke University Medical Center, Durham, NC 27710 USA.ORCID 0000-0001-8261-2235

Funding

DART.3-Revolutionizing Neuropsychiatric Treatment through Noninvasive, Programmable Cell-Type-Specific NeuropharmacologyR01MH135932 · NIMH · DUKE UNIVERSITY · PI Michael R Tadross · 2024 to 2026
$4.4M
DART2.0: comprehensive cell type-specific behavioral neuropharmacologyRF1MH117055 · NIMH · DUKE UNIVERSITY · PI TADROSS, MICHAEL R · 2018 to 2018
$3.8M
Evaluating cell type-specific non-dopaminergics as a Parkinson's treatment paradigmR01NS107472 · NINDS · DUKE UNIVERSITY · PI TADROSS, MICHAEL R · 2018 to 2022
$1.7M
Interrogating the cholinergic basis of opioid use disorderR61DA051530 · NIDA · DUKE UNIVERSITY · PI TADROSS, MICHAEL R · 2020 to 2022
$1.4M
Linking cortical circuit computations to visual perceptionR01EY031716 · NEI · DUKE UNIVERSITY · PI GLICKFELD, LINDSEY L · 2022 to 2024
$1.3M
Dissecting cholinergic modulation of interneurons underlying state-dependent processing in mouse visual cortexF32EY034013 · NEI · DUKE UNIVERSITY · PI CAMMARATA, CELINE · 2023 to 2025
$229k
Mechanisms underlying rapid adaptation in mouse visual cortexF31EY031941 · NEI · DUKE UNIVERSITY · PI LI, JENNIFER YING · 2020 to 2022
$113k
NEI NIH HHS F31 EY031941NEI NIH HHS F32 EY034013NEI NIH HHS R01 EY031716NIDA NIH HHS R61 DA051530NIMH NIH HHS RF1 MH117055NINDS NIH HHS R01 NS107472
6 · The paper itself

Abstract

Inhibition stabilization enables cortical circuits to encode sensory signals across diverse contexts. Somatostatin-expressing (SST) interneurons are well-suited for this role through their strong recurrent connectivity with excitatory pyramidal cells. We developed a cortical circuit model predicting that SST cells become increasingly important for stabilization as sensory input strengthens. We tested this prediction in mouse primary visual cortex by manipulating excitatory input to SST cells, a key parameter for inhibition stabilization, with a novel cell-type specific pharmacological method to selectively block glutamatergic receptors on SST cells. Consistent with our model predictions, we find antagonizing glutamatergic receptors drives a paradoxical facilitation of SST cells with increasing stimulus contrast. In addition, we find even stronger engagement of SST-dependent stabilization when the mice are aroused. Thus, we reveal that the role of SST cells in cortical processing gradually switches as a function of both input strength and behavioral state.

Indexed as

AMPA receptorscalcium imagingchemogeneticsinhibitionmicrocircuitnormalizationpharmacologyvisual cortex

Identifiers

PMID39314375
PMCPMC11419099

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.