Evidence map›Paper›PMID 34920732›Full record

ArticleBehavioral and brain functions : BBF2021

NLRP1 inflammasome involves in learning and memory impairments and neuronal damages during aging process in mice.

Dan Sun, Guofang Gao, Bihua Zhong, Han Zhang, Shixin Ding, Zhenghao Sun, Yaodong Zhang, Weizu Li

Open access · goldAbstract read
In one paragraph

Article in Behavioral and brain functions : BBF, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
2.3field-weighted citation impact, top 11% 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

18 citing papers in PubMed, 31 citations in OpenAlex.

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  7. Inflammasomes in neurodegenerative diseases.Translational neurodegeneration · 2024
    Review
  8. Study on the Mechanisms of Glrα3 in Pain Sensitization of Endometriosis.International journal of molecular sciences · 2024
    Article
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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

8 authors at 2 institutions in 1 country.

Dan Sun *Department of Pharmacy, The First People's Hospital of Xiaoshan District, 199 Shixin South Road, Hangzhou, 311200, Zhejiang, China.
Guofang Gao *Department of Pharmacy, The First People's Hospital of Xiaoshan District, 199 Shixin South Road, Hangzhou, 311200, Zhejiang, China.
Bihua Zhong *Department of Pharmacy, The First People's Hospital of Xiaoshan District, 199 Shixin South Road, Hangzhou, 311200, Zhejiang, China.
Han ZhangDepartment of Pharmacology, Basic Medicine College, Anhui Medical University, No. 81 Meishan Road, Hefei, 230032, Anhui, China.
Shixin DingDepartment of Pharmacology, Basic Medicine College, Anhui Medical University, No. 81 Meishan Road, Hefei, 230032, Anhui, China.
Zhenghao SunDepartment of Pharmacology, Basic Medicine College, Anhui Medical University, No. 81 Meishan Road, Hefei, 230032, Anhui, China.
Yaodong ZhangDepartment of Pharmacy, The First People's Hospital of Xiaoshan District, 199 Shixin South Road, Hangzhou, 311200, Zhejiang, China.
Weizu LiDepartment of Pharmacology, Basic Medicine College, Anhui Medical University, No. 81 Meishan Road, Hefei, 230032, Anhui, China. liweizu@126.com.ORCID http://orcid.org/0000-0002-8305-1414
Anhui Medical University · CNThe First People's Hospital of Xiaoshan District, Hangzhou · CN

Funding

national natural science foundation of china 81671384national natural science foundation of china 81970630
6 · The paper itself

Abstract

backgroundBrain aging is an important risk factor in many human diseases, such as Alzheimer's disease (AD). The production of excess reactive oxygen species (ROS) mediated by nicotinamide adenine dinucleotide phosphate oxidase 2 (NOX2) and the maturation of inflammatory cytokines caused by activation of the NOD-like receptor protein 1 (NLRP1) inflammasome play central roles in promoting brain aging. However, it is still unclear when and how the neuroinflammation appears in the brain during aging process.

methodsIn this study, we observed the alterations of learning and memory impairments, neuronal damage, NLRP1 inflammasome activation, ROS production and NOX2 expression in the young 6-month-old (6 M) mice, presenile 16 M mice, and older 20 M and 24 M mice.

resultsThe results indicated that, compared to 6 M mice, the locomotor activity, learning and memory abilities were slightly decreased in 16 M mice, and were significantly decreased in 20 M and 24 M mice, especially in the 24 M mice. The pathological results also showed that there were no significant neuronal damages in 6 M and 16 M mice, while there were obvious neuronal damages in 20 M and 24 M mice, especially in the 24 M group. Consistent with the behavioral and histological changes in the older mice, the activity of β-galactosidase (β-gal), the levels of ROS and IL-1β, and the expressions of NLRP1, ASC, caspase-1, NOX2, p47phox and p22phox were significantly increased in the cortex and hippocampus in the older 20 M and 24 M mice.

conclusionOur study suggested that NLRP1 inflammasome activation may be closely involved in aging-related neuronal damage and may be an important target for preventing brain aging.

Indexed as

Adaptor Proteins, Signal TransducingAgingApoptosis Regulatory ProteinsInflammasomesNLR ProteinsAnimalsLearningMemory DisordersMiceNeuroinflammatory DiseasesNeuronsAdaptor Proteins, Signal TransducingApoptosis Regulatory ProteinsInflammasomesNALP1 protein, mouseNLR ProteinsBrain agingLearning and memory impairmentsNADPH oxidase 2NLRP1 inflammasomeROS

Identifiers

PMID34920732
PMCPMC8680336
OpenAlexW4200330627

What OpenQuestion holds

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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 OpenQuestion graph.