Evidence map›Paper›PMID 37725102›Full record

ReviewInflammation research : official journal of the European Histamine Research Society ... [et al.]2023

Role of NLRP3 inflammasome-mediated neuronal pyroptosis and neuroinflammation in neurodegenerative diseases.

Ying-Hao Han, Xiao-Dong Liu, Mei-Hua Jin, Hu-Nan Sun, Taeho Kwon

Abstract readReview
PubMed Publisher
In one paragraph

Review in Inflammation research : official journal of the European Histamine Research Society ... [et al.], 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 55 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
55citing papers in PubMed, 3 pooled it
12.5field-weighted citation impact, top 1% 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

55 citing papers in PubMed, 3 syntheses or guidelines pooled it, 81 citations in OpenAlex.

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  7. Life (Basel, Switzerland) · 2026
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  19. Non-canonical cell death in neurodegeneration: emerging mechanisms and therapeutic Frontiers.Apoptosis : an international journal on programmed cell death · 2026
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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

5 authors at 2 institutions in 2 countries.

Ying-Hao Han *College of Life Science & Biotechnology, Heilongjiang Bayi Agricultural University, Daqing, 163319, China. hyhbynd@163.com.
Xiao-Dong Liu *College of Life Science & Biotechnology, Heilongjiang Bayi Agricultural University, Daqing, 163319, China.
Mei-Hua JinCollege of Life Science & Biotechnology, Heilongjiang Bayi Agricultural University, Daqing, 163319, China.
Hu-Nan SunCollege of Life Science & Biotechnology, Heilongjiang Bayi Agricultural University, Daqing, 163319, China. sunhunan76@163.com.
Taeho KwonPrimate Resources Center, Korea Research Institute of Bioscience and Biotechnology (KRIBB), Jeongeup-si, Jeonbuk, 56216, Republic of Korea. kwon@kribb.re.kr.
Heilongjiang Bayi Agricultural University · CNKorea Research Institute of Bioscience and Biotechnology · KR

Funding

KRIBB Research Initiative Program KGM5162322
6 · The paper itself

Abstract

backgroundNeurodegenerative diseases are a common group of neurological disorders characterized by progressive loss of neuronal structure and function leading to cognitive impairment. Recent studies have shown that neuronal pyroptosis mediated by the NLRP3 inflammasome plays a crucial role in the pathogenesis of neurodegenerative diseases. OBJECTIVE AND

methodThe NLRP3 inflammasome is a multiprotein complex that, when activated within cells, triggers an inflammatory response, ultimately leading to pyroptotic cell death of neurons. Pyroptosis is a typical pro-inflammatory programmed cell death process occurring downstream of NLRP3 inflammasome activation, characterized by the formation of pores on the cell membrane by the GSDMD protein, leading to cell lysis and the release of inflammatory factors. It has been found that NLRP3 inflammasome-mediated neuronal pyroptosis is closely associated with the development of various neurodegenerative diseases, such as Alzheimer's disease, traumatic brain injury, and Parkinson's disease. Therefore, inhibiting NLRP3 inflammasome activation and attenuating neuronal pyroptosis could potentially serve as novel strategies for the treatment of neurodegenerative diseases.

resultsThe aim of this review is to explore the role of NLRP3 activation-mediated neuronal pyroptosis and neuroinflammation in neurodegenerative diseases. Firstly, we extensively discuss the relationship between NLRP3 inflammasome-mediated neuronal pyroptosis and neuroinflammation in various neurodegenerative diseases. Subsequently, we further explore the mechanisms driving NLRP3 activation and assembly, as well as the post-translational modifications regulating NLRP3 inflammasome activation.

conclusionUnderstanding these mechanisms will contribute to a deeper understanding of the link between neuronal pyroptosis and neurodegenerative diseases, and hold significant implications for the treatment and prevention of neurodegenerative diseases.

Indexed as

Neurodegenerative DiseasesHumansInflammasomesNeuroinflammatory DiseasesNeuronsNLR Family, Pyrin Domain-Containing 3 ProteinPyroptosisInflammasomesNLR Family, Pyrin Domain-Containing 3 ProteinNeurodegenerative diseasesNeuroinflammationNeuronNLRP3 inflammasomePost-translational regulationPyroptosis

Identifiers

PMID37725102
OpenAlexW4386846297

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.