Evidence map›Paper›PMID 36522512›Full record

ArticleActa pharmacologica Sinica2023

Scoparone suppresses mitophagy-mediated NLRP3 inflammasome activation in inflammatory diseases.

Wan-di Feng, Yao Wang, Tong Luo, Xin Jia, Cui-Qin Cheng, Hao-Jia Wang, Mei-Qi Zhang, Qi-Qi Li, Xue-Jiao Wang, Yi-Ying Li and 4 more

Open access · greenAbstract read
In one paragraph

Article in Acta pharmacologica Sinica, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed, 1 pooled it
2.8field-weighted citation impact, top 8% 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

23 citing papers in PubMed, 1 synthesis or guideline pooled it, 34 citations in OpenAlex.

  1. Pooled it
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  20. 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

14 authors at 1 institution in 1 country.

Wan-di Feng *Beijing Research Institute of Chinese Medicine, Beijing University of Chinese Medicine, Beijing, 100029, China.
Yao Wang *Department of Immunology, School of Life Science, Beijing University of Chinese Medicine, Beijing, 100029, China.
Tong Luo *Department of Immunology, School of Life Science, Beijing University of Chinese Medicine, Beijing, 100029, China.
Xin JiaDepartment of Pharmacology, School of Chinese Materia Medica, Beijing University of Chinese Medicine, Beijing, 100029, China.
Cui-Qin ChengDepartment of Immunology, School of Life Science, Beijing University of Chinese Medicine, Beijing, 100029, China.
Hao-Jia WangDepartment of Immunology, School of Life Science, Beijing University of Chinese Medicine, Beijing, 100029, China.
Mei-Qi ZhangDepartment of Pharmacology, School of Chinese Materia Medica, Beijing University of Chinese Medicine, Beijing, 100029, China.
Qi-Qi LiDepartment of Pharmacology, School of Chinese Materia Medica, Beijing University of Chinese Medicine, Beijing, 100029, China.
Xue-Jiao WangDepartment of Immunology, School of Life Science, Beijing University of Chinese Medicine, Beijing, 100029, China.
Yi-Ying LiDepartment of Immunology, School of Life Science, Beijing University of Chinese Medicine, Beijing, 100029, China.
Jin-Yong WangDepartment of Pharmacology, School of Chinese Materia Medica, Beijing University of Chinese Medicine, Beijing, 100029, China.
Guang-Rui HuangDepartment of Immunology, School of Life Science, Beijing University of Chinese Medicine, Beijing, 100029, China.
Ting WangBeijing Research Institute of Chinese Medicine, Beijing University of Chinese Medicine, Beijing, 100029, China.
An-Long XuBeijing Research Institute of Chinese Medicine, Beijing University of Chinese Medicine, Beijing, 100029, China. xuanlong@bucm.edu.cn.
Beijing University of Chinese Medicine · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Recent evidence shows that targeting NLRP3 inflammasome activation is an important means to treat inflammasome-driven diseases. Scoparone, a natural compound isolated from the Chinese herb Artemisia capillaris Thunb, has anti-inflammatory activity. In this study we investigated the effect of scoparone on NLRP3 inflammasome activation in inflammatory diseases. In LPS-primed, ATP or nigericin-stimulated mouse macrophage J774A.1 cells and bone marrow-derived macrophages (BMDMs), pretreatment with scoparone (50 μM) markedly restrained canonical and noncanonical NLRP3 inflammasome activation, evidenced by suppressed caspase-1 cleavage, GSDMD-mediated pyroptosis, mature IL-1β secretion and the formation of ASC specks. We then conducted a transcriptome analysis in scoparone-pretreated BMDMs, and found that the differentially expressed genes were significantly enriched in mitochondrial reactive oxygen species (ROS) metabolic process, mitochondrial translation and assembly process, as well as in inflammatory response. We demonstrated in J774A.1 cells and BMDMs that scoparone promoted mitophagy, a well-characterized mechanism to control mitochondrial quality and reduce ROS production and subsequent NLRP3 inflammasome activation. Mitophagy blockade by 3-methyladenine (3-MA, 5 mM) reversed the protective effects of scoparone on mitochondrial damage and inflammation in the murine macrophages. Moreover, administration of scoparone (50 mg/kg) exerted significant preventive effects via inhibition of NLRP3 activation in mouse models of bacterial enteritis and septic shock. Collectively, scoparone displays potent anti-inflammatory effects via blocking NLRP3 inflammasome activation through enhancing mitophagy, highlighting a potential action mechanism in treating inflammasome-related diseases for further clinical investigation.

Indexed as

InflammasomesNLR Family, Pyrin Domain-Containing 3 ProteinAnimalsAnti-Inflammatory AgentsCoumarinsInterleukin-1betaLipopolysaccharidesMiceMice, Inbred C57BLMitophagyReactive Oxygen SpeciesAnti-Inflammatory AgentsCoumarinsInflammasomesInterleukin-1betaLipopolysaccharidesNLR Family, Pyrin Domain-Containing 3 ProteinNlrp3 protein, mouseReactive Oxygen Speciesscoparone3-methyladenineIL-1βinflammatory diseasemitophagyNLRP3 inflammasomescoparone

Identifiers

PMID36522512
PMCPMC10203299
OpenAlexW4311673589

What OpenQuestion holds

Textmetadata
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.