Evidence map›Paper›PMID 42776972›Full record

ArticlePloS one2026

The limited role of RGS10 on NFκB and cytokine transcript levels in peritoneal macrophages under the influence of opioid analgesics.

Janna E Jernigan Posey, Kruthika Dheeravath, Cassandra L Cole, Noelle K Neighbarger, Kelly B Menees, Malú Gámez Tansey

Abstract read
In one paragraph

Article in PloS one, 2026. 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
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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

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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

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.

Janna E Jernigan PoseyCenter for Translational Research in Neurodegenerative Disease, College of Medicine, University of Florida, Gainesville, Florida, United States of America.ORCID https://orcid.org/0000-0003-0771-384X
Kruthika DheeravathCenter for Translational Research in Neurodegenerative Disease, College of Medicine, University of Florida, Gainesville, Florida, United States of America.
Cassandra L ColeCenter for Translational Research in Neurodegenerative Disease, College of Medicine, University of Florida, Gainesville, Florida, United States of America.
Noelle K NeighbargerCenter for Translational Research in Neurodegenerative Disease, College of Medicine, University of Florida, Gainesville, Florida, United States of America.ORCID https://orcid.org/0009-0007-6649-0988
Kelly B MeneesCenter for Translational Research in Neurodegenerative Disease, College of Medicine, University of Florida, Gainesville, Florida, United States of America.
Malú Gámez TanseyCenter for Translational Research in Neurodegenerative Disease, College of Medicine, University of Florida, Gainesville, Florida, United States of America.ORCID https://orcid.org/0000-0002-1719-4708

Funding

Interdisciplinary Training in Movement Disorders and NeurorestorationT32NS082168 · NINDS · UNIVERSITY OF FLORIDA · PI Melissa Jo Armstrong, David E Vaillancourt · 2015 to 2026
$2.8M
Training Grant on Alzheimer's Disease and ADRD at Indiana UniversityT32AG071444 · NIA · INDIANA UNIVERSITY INDIANAPOLIS · PI GARY E. LANDRETH, Bruce T Lamb · 2021 to 2026
$2.8M
NIA NIH HHS T32 AG071444NINDS NIH HHS T32 NS082168
6 · The paper itself

Abstract

Regulator of G-protein signaling 10 (RGS10) has been shown to regulate multiple inflammatory pathways relevant to disease pathogenesis. Of particular importance is the ability of RGS10 to negatively regulate the NFkB pathway, a prominent pro-inflammatory pathway implicated in multiple inflammatory disease phenotypes. However, the exact mechanism by which RGS10 regulates NFκB is unknown. Given that RGS10 translocates to the nucleus upon stimulation, we hypothesize that RGS10 may regulate NFκB at the transcript level. To determine whether RGS10 influences NFκB transcript levels, we stimulated peritoneal macrophages from RGS10 Knockout (KO) and B6 mice and collected cell lysate and conditioned media over a 24-hour period to assess transcript levels of NFκB and related pro-inflammatory cytokines as well as secreted cytokine levels. Here we found a limited and transient influence of RGS10 on transcript levels of NFκB subunits and NFκB-dependent cytokines. However, RGS10 displayed a more robust negative regulation of secreted protein levels of certain pro-inflammatory cytokines. Importantly, this study required the use of opioid analgesics prior to the collection of peritoneal macrophages and therefore reflects the role of RGS10 on pro-inflammatory transcript and protein levels when opioid analgesics are present. Overall, this study indicates that RGS10 may not serve as an important transcriptional regulator of NFκB related cytokine production under the influence of opioid analgesics. Further studies are warranted to understand the influence of opioid analgesics on RGS10 function and the mechanism by which RGS10 regulates NFκB activity.

Indexed as

Analgesics, OpioidCytokinesMacrophages, PeritonealNF-kappa BRGS ProteinsAnimalsGene Expression RegulationMiceMice, Inbred C57BLMice, KnockoutRNA, MessengerAnalgesics, OpioidCytokinesNF-kappa BRgs10 protein, mouseRGS ProteinsRNA, Messenger

Identifiers

PMID42776972
PMCPMC13600522

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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.