Evidence map›Paper›PMID 31267316›Full record

ArticleJournal of molecular neuroscience : MN2019

Effects of NLRP6 in Cerebral Ischemia/Reperfusion (I/R) Injury in Rats.

Changchang Meng, Jinyan Zhang, Luyu Zhang, Yueting Wang, Zhenyu Li, Jing Zhao

Abstract read
PubMed Publisher
In one paragraph

Article in Journal of molecular neuroscience : MN, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
2.7field-weighted citation impact, top 9% 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, 50 citations in OpenAlex.

  1. Review
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  17. Review
  18. The NLRP6 inflammasome.Immunology · 2021
    Review
  19. Review
  20. Article
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

6 authors at 1 institution in 1 country.

Changchang MengDepartment of Pathophysiology, Institute of Neuroscience, Chongqing Medical University, Road1, Chongqing, 400016, People's Republic of China.
Jinyan ZhangDepartment of Pathology, Chongqing Medical University, Chongqing, People's Republic of China.
Luyu ZhangDepartment of Molecular Medicine, Chongqing Medical University, Chongqing, People's Republic of China.
Yueting WangDepartment of Pathophysiology, Institute of Neuroscience, Chongqing Medical University, Road1, Chongqing, 400016, People's Republic of China.
Zhenyu LiDepartment of Pathology, Chongqing Medical University, Chongqing, People's Republic of China.
Jing ZhaoDepartment of Pathophysiology, Institute of Neuroscience, Chongqing Medical University, Road1, Chongqing, 400016, People's Republic of China. zhaojing@cqmu.edu.cn.ORCID http://orcid.org/0000-0002-1980-280X
Chongqing Medical University · CN

Funding

Natural Science Foundation of Chongqing No.cstc2015jcyA10048The National Natural Science Foundation of China Nos.81671158 and 81771261
6 · The paper itself

Abstract

The NOD-like receptor protein 6 (NLRP6), an intracytoplasmic pattern recognition receptor in the nucleotide-binding domain, leucine-rich repeat-containing (NLR) innate immune receptor family, influences the inflammation reaction. The role of NLRP6 in cerebral ischemia-reperfusion (I/R) injury in rats is unclear. We explore the function of NLRP6 in cerebral I/R injury. The investigators used a middle cerebral artery occlusion/reperfusion model (MCAO) to imitate ischemic injury. We found the peak expression of NLRP6 is in 48-h post-cerebral I/R injury. The expression of NLRP6 siRNA, as well as the expression of protein and mRNA, was detected by Western blot and qRT-PCR. The degree of IL-1β and IL-18 was assessed by ELISA. After downregulating NLRP6, the expression of IL-1β, IL-18, cleaved Caspase-1, and myeloperoxidase (MPO) were reduced. In HE and Nissl staining, pathological injury of brain tissue after downregulating NLRP6 was improved. NLRP6 siRNA decreased the NLRP6-ASC binding states by CO-IP. NRP6 has a pro-inflammatory effect in cerebral I/R injury, which may provide a new target for the treatment of cerebral I/R injury.

Indexed as

AnimalsBrainBrain EdemaCaspase 1Gene Expression RegulationInfarction, Middle Cerebral ArteryInflammationInterleukin-18Interleukin-1betaMaleNerve Tissue ProteinsRandom AllocationRatsRats, Sprague-DawleyReceptors, AngiotensinReceptors, VasopressinCaspase 1Interleukin-18Interleukin-1betaNerve Tissue ProteinsNlrp6 protein, ratReceptors, AngiotensinReceptors, VasopressinRNA, MessengerRNA, Small InterferingCerebral ischemia/reperfusion injuryIL (interleukin)-18IL (interleukin)-1βInflammationNLRP6

Identifiers

PMID31267316
OpenAlexW2954989732

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.