Evidence map›Paper›PMID 33446652›Full record

ArticleTranslational psychiatry2021

Anxiolytic effects of NLRP3 inflammasome inhibition in a model of chronic sleep deprivation.

Chad Smith, Kyle J Trageser, Henry Wu, Francis J Herman, Umar Haris Iqbal, Maria Sebastian-Valverde, Tal Frolinger, Emma Zeng, Giulio Maria Pasinetti

Open access · goldAbstract read
In one paragraph

Article in Translational psychiatry, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.8field-weighted citation impact, top 17% 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

18 citing papers in PubMed, 37 citations in OpenAlex.

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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

9 authors at 2 institutions in 1 country.

Chad SmithDepartment of Neurology, Icahn School of Medicine at Mount Sinai, New York, New York, 10029, USA.
Kyle J TrageserDepartment of Neurology, Icahn School of Medicine at Mount Sinai, New York, New York, 10029, USA.ORCID 0000-0001-9161-0178
Henry WuDepartment of Neurology, Icahn School of Medicine at Mount Sinai, New York, New York, 10029, USA.
Francis J HermanDepartment of Neurology, Icahn School of Medicine at Mount Sinai, New York, New York, 10029, USA.
Umar Haris IqbalDepartment of Neurology, Icahn School of Medicine at Mount Sinai, New York, New York, 10029, USA.
Maria Sebastian-ValverdeDepartment of Neurology, Icahn School of Medicine at Mount Sinai, New York, New York, 10029, USA.
Tal FrolingerDepartment of Neurology, Icahn School of Medicine at Mount Sinai, New York, New York, 10029, USA.
Emma ZengDepartment of Neurology, Icahn School of Medicine at Mount Sinai, New York, New York, 10029, USA.
Giulio Maria PasinettiDepartment of Neurology, Icahn School of Medicine at Mount Sinai, New York, New York, 10029, USA. giulio.pasinetti@mssm.edu.ORCID 0000-0002-1524-5196
Icahn School of Medicine at Mount Sinai · USGeriatric Research Education and Clinical Center · US

Funding

Pasinetti: Project 3; Role of Microbiome in Promotion of Cognitive and Psychological Resilience (Faith)P50AT008661 · NCCIH · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI PASINETTI, GIULIO MARIA · 2015 to 2019
$11.2M
Suppression of Immune Signatures of Stress by Polyphenols SupplementsU19AT010835 · NCCIH · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI SIMON, JAMES E · 2020 to 2024
$6.8M
BLRD VA I01 BX004583BLRD VA IK6 BX003785NCCIH NIH HHS P50 AT008661NCCIH NIH HHS U19 AT010835U.S. Department of Health & Human Services | NIH | National Center for Complementary and Integrative Health (NCCIH) AT008661-01
6 · The paper itself

Abstract

Sleep deprivation is a form of stress that provokes both inflammatory responses and neuropsychiatric disorders. Because persistent inflammation is implicated as a physiological process in anxiety disorders, we investigated the contributions of NLRP3 inflammasome signaling to anxiety and anxiolytic properties of flavanol diets in a model of chronic sleep deprivation. The results show a flavanol-rich dietary preparation (FDP) exhibits anxiolytic properties by attenuating markers of neuroimmune activation, which included IL-1β upregulation, NLRP3 signaling, and microglia activation in the cortex and hippocampus of sleep-deprived mice. Production of IL-1β and NLRP3 were critical for both anxiety phenotypes and microglia activation. Individual FDP metabolites potently inhibited IL-1β production from microglia following stimulation with NLRP3-specific agonists, supporting anxiolytic properties of FDP observed in models of sleep deprivation involve inhibition of the NLRP3 inflammasome. The study further showed sleep deprivation alters the expression of the circadian gene Bmal1, which critically regulated NLRP3 expression and IL-1β production.

Indexed as

Anti-Anxiety AgentsInflammasomesAnimalsInterleukin-1betaMiceMicrogliaNLR Family, Pyrin Domain-Containing 3 ProteinSleep DeprivationAnti-Anxiety AgentsInflammasomesInterleukin-1betaNLR Family, Pyrin Domain-Containing 3 ProteinNlrp3 protein, mouse

Identifiers

PMID33446652
PMCPMC7809257
OpenAlexW3119774076

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.