Evidence map›Paper›PMID 40305196›Full record

ArticleBiomolecules2025

Probenecid Inhibits NLRP3 Inflammasome Activity and Mitogen-Activated Protein Kinases (MAPKs).

Les P Jones, David E Martin, Jackelyn Murray, Fred Sancilio, Ralph A Tripp

Abstract read
In one paragraph

Article in Biomolecules, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 1 pooled it
–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

7 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. The MAPK Response to Virus Infection Is Modified by Probenecid.Current issues in molecular biology · 2025
    Review
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

5 authors.

Les P JonesDepartment of Infectious Diseases, University of Georgia, Athens, GA 30602, USA.
David E MartinTrippBio, Inc., Jacksonville, FL 32256, USA.ORCID 0000-0003-2820-5983
Jackelyn MurrayDepartment of Infectious Diseases, University of Georgia, Athens, GA 30602, USA.
Fred SancilioDepartment of Chemistry and Biochemistry, Florida Atlantic University, Jupiter, FL 33431, USA.
Ralph A TrippDepartment of Infectious Diseases, University of Georgia, Athens, GA 30602, USA.ORCID 0000-0002-2924-9956

Funding

Georgia Research Alliance endowment
6 · The paper itself

Abstract

Probenecid has long been a versatile drug in pharmacological therapies, primarily known for blocking active tubular secretion in the kidney, affecting both endogenous substances like uric acid and exogenous ones like penicillin. Beyond its renal applications, probenecid has shown capabilities in crossing the blood-brain barrier and modulating the activity of various membrane channels and transporters. This compound has emerged as a potent antiviral agent, demonstrating efficacy against multiple viruses, including influenza, COVID-19, and RSV. Clinical trials with COVID-19 patients have confirmed its antiviral potential, sparking further investigation into its mechanisms of action. This study explores probenecid's significant anti-inflammatory properties, focusing on its ability to inhibit inflammasome activation. Our study aims to unravel the anti-inflammatory effects of probenecid on the NLRP3 inflammasome and MAPK signaling pathways using murine macrophages as a relevant inflammation model. We reveal that probenecid treatment blocks JNK and ERK signaling without affecting p38 MAPK, suppressing NLRP3 inflammasome activation. Additionally, probenecid does not affect NFκB-directed protein expression, although it efficiently inhibits NLRP3 inflammasome outputs, e.g., IL-1β and pyroptosis. These results indicate probenecid's potential therapeutic applications.

Indexed as

Anti-Inflammatory AgentsInflammasomesMitogen-Activated Protein KinasesNLR Family, Pyrin Domain-Containing 3 ProteinProbenecidAnimalsHumansInterleukin-1betaMacrophagesMAP Kinase Signaling SystemMiceAnti-Inflammatory AgentsInflammasomesInterleukin-1betaMitogen-Activated Protein KinasesNLR Family, Pyrin Domain-Containing 3 ProteinNlrp3 protein, mouseProbenecidanti-inflammatoryantiviralhost-directedinflammasomeJ774A.1 mouse macrophages

Identifiers

PMID40305196
PMCPMC12024562

What Socratic 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 Socratic graph.