Evidence map›Paper›PMID 37772394›Full record

ArticleMolecular medicine reports2023

Kynurenic acid inhibits macrophage pyroptosis by suppressing ROS production via activation of the NRF2 pathway.

Yuwei Gao, Xiaohui Guo, Yunpeng Zhou, Jie Du, Chengbo Lu, Lei Zhang, Siyuan Sun, Shengfang Wang, Yang Li

Open access · hybridAbstract read
In one paragraph

Article in Molecular medicine reports, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
4.2field-weighted citation impact, top 5% 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

21 citing papers in PubMed, 27 citations in OpenAlex.

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  17. Pharmaceuticals (Basel, Switzerland) · 2024
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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 5 institutions in 1 country.

Yuwei GaoDepartment of Pediatric Dentistry, Jiamusi University Affiliated Stomatological Hospital, Jiamusi, Heilongjiang 154000, P.R. China.
Xiaohui GuoDepartment of Pathology, First Affiliated Hospital of Anhui Medical University, Hefei, Anhui 230022, P.R. China.
Yunpeng ZhouDepartment of Urology, Tianjin Baodi Hospital, Baodi Clinical College of Tianjin Medical University, Tianjin 300203, P.R. China.
Jie DuDepartment of Cardiology, The Second Affiliated Hospital of Harbin Medical University, Harbin, Heilongjiang 150001, P.R. China.
Chengbo LuDepartment of Cardiology, The First Affiliated Hospital of Jiamusi University, Jiamusi, Heilongjiang 154002, P.R. China.
Lei ZhangDepartment of Cardiology, People's Hospital of Taihe County, Taihe, Anhui 236600, P.R. China.
Siyuan SunDepartment of Cardiology, People's Hospital of Taihe County, Taihe, Anhui 236600, P.R. China.
Shengfang WangDepartment of Cardiology, The Second Affiliated Hospital of Harbin Medical University, Harbin, Heilongjiang 150001, P.R. China.
Yang LiDepartment of Cardiology, The Fourth Affiliated Hospital of Harbin Medical University, Harbin, Heilongjiang 150001, P.R. China.
Harbin Medical University · CNAnhui Medical University · CNFirst Affiliated Hospital of Jiamusi University · CNJiamusi University · CNTianjin Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Macrophage pyroptosis and related inflammatory responses play an important role in periodontitis. Kynurenic acid (KA) is hypothesized to have anti‑inflammatory potential, but whether KA can inhibit macrophage pyroptosis and the underlying mechanisms remain unclear. Lipopolysaccharide (LPS) was used to induce pyroptosis in THP‑1‑derived macrophages. KA or ML385 was used to pretreat macrophages, after which, cell viability, NOD‑like receptor protein 3 (NLRP3) inflammasome‑related protein expression, oxidative stress levels and nuclear factor erythroid 2‑related factor 2 (NRF2) expression were measured. The results showed that KA improved the LPS‑induced decrease in macrophage viability and lactate dehydrogenase release. KA prevented THP‑1 macrophage pyroptosis induced by LPS by reducing the expression of NLRP3, Gasdermin‑D, and Caspase1, and decreased the expression of inflammatory factors. KA suppressed NLRP3 inflammasome activation by inhibiting ROS overproduction and increasing Heme Oxygenase 1 and glutathione levels. Moreover, KA promoted NRF2 translocation from the cytoplasm to the nucleus. In addition, the anti‑pyroptotic and antioxidant effects of KA were reversed by ML385 inhibition of NRF2. In the present study, it was found that KA significantly suppressed macrophage pyroptosis induced by LPS. It was further demonstrated that the anti‑pyroptotic effects of KA were mediated by activation of the NRF2 pathway.

Indexed as

InflammasomesKynurenic AcidNLR Family, Pyrin Domain-Containing 3 ProteinLipopolysaccharidesMacrophagesNF-E2-Related Factor 2PyroptosisReactive Oxygen SpeciesSignal TransductionInflammasomesKynurenic AcidLipopolysaccharidesNF-E2-Related Factor 2NLR Family, Pyrin Domain-Containing 3 ProteinReactive Oxygen Specieskynurenic acidmacrophagesoxidative stressperiodontitispyroptosis

Identifiers

PMID37772394
PMCPMC10552067
OpenAlexW4386961739

What OpenQuestion holds

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Registered trials

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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.