Evidence map›Paper›PMID 31732924›Full record

ArticleJournal of molecular neuroscience : MN2020

The Cannabinoid WIN 55,212-2 Reduces Delayed Neurologic Sequelae After Carbon Monoxide Poisoning by Promoting Microglial M2 Polarization Through ST2 Signaling.

Jing-Jing Du, Zhi-Qin Liu, Yue Yan, Jing Xiong, Xiao-Tao Jia, Zheng-Li Di, Jing-Jing Ren

Abstract read
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In one paragraph

Article in Journal of molecular neuroscience : MN, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.8field-weighted citation impact, top 26% 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

5 citing papers in PubMed, 12 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Interleukin-33 regulates the functional state of microglia.Frontiers in cellular neuroscience · 2022
    Review
  5. CB2 Receptor in Microglia: The Guardian of Self-Control.International journal of molecular sciences · 2020
    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

7 authors at 1 institution in 1 country.

Jing-Jing DuDepartment of Neurology, Xi'an Central Hospital, Xi'an Jiaotong University, Xi'an, 710054, China.
Zhi-Qin LiuDepartment of Neurology, Xi'an Central Hospital, Xi'an Jiaotong University, Xi'an, 710054, China.
Yue YanDepartment of Neurology, Xi'an Central Hospital, Xi'an Jiaotong University, Xi'an, 710054, China.
Jing XiongDepartment of Neurology, Xi'an Central Hospital, Xi'an Jiaotong University, Xi'an, 710054, China.
Xiao-Tao JiaDepartment of Neurology, Xi'an Central Hospital, Xi'an Jiaotong University, Xi'an, 710054, China.
Zheng-Li DiDepartment of Neurology, Xi'an Central Hospital, Xi'an Jiaotong University, Xi'an, 710054, China.
Jing-Jing RenDepartment of Hematology, Xi'an Central Hospital, Xi'an Jiaotong University, Xi'an, 710054, China. renjing_orange@126.com.ORCID http://orcid.org/0000-0003-2582-659X
Xian Central Hospital · CN

Funding

National Natural Science Foundation of China 81501139
6 · The paper itself

Abstract

Delayed neurologic sequelae (DNS) are among the most serious complications of carbon monoxide (CO) poisoning caused partly by elevated neuroinflammation. WIN 55,212-2, a non-selective agonist of cannabinoid receptors, has been demonstrated to have anti-inflammatory properties in various brain disorders. The anti-inflammatory action of WIN 55,212-2 is potentially associated with driving microglial M2 polarization. ST2 signaling is important in regulating inflammatory responses and microglial polarization. Therefore, we aimed to investigate the neuroprotective effect of WIN 55,212-2 on DNS after CO poisoning and elucidate its relationship with ST2-mediated microglial M2 polarization. The behavioral tests showed that treatment with WIN 55,212-2 significantly ameliorates the cognitive impairment induced by CO poisoning. This behavioral improvement was accompanied by reduced neuron loss, decreased production of pro-inflammatory cytokines, and a limited number of microglia in the hippocampus. Moreover, WIN 55,212-2 elevated the protein expression of IL-33 (the ligand of ST2) and ST2, increased the ratio of CD206-positive (M2 phenotype) and ST2-positive microglia, and augmented production of M2 microglia-associated cytokines in the hippocampus of CO-exposed rats. Furthermore, we observed that the WIN 55,212-2-mediated increases in ST2 protein expression, CD206-positive and ST2-positive microglia, and microglia-associated cytokines were blocked by the cannabinoid receptor 2 (CB2R) antagonist AM630 but not by the cannabinoid receptor 1 (CB1R) antagonist AM251. In contrast, the WIN 55,212-2-induced upregulation of the IL-33 protein expression was inhibited by AM251 but not by AM630. Altogether, these findings reveal cannabinoid receptors as promising therapeutic agents for CO poisoning and identify ST2 signaling-related microglial M2 polarization as a new mechanism of cannabinoid-induced neuroprotection.

Indexed as

Signal TransductionAnimalsBenzoxazinesCannabinoidsCarbon Monoxide PoisoningCognitionInterleukin-1 Receptor-Like 1 ProteinInterleukin-33Lectins, C-TypeMaleMannose-Binding LectinsMannose ReceptorMicrogliaMorpholinesNaphthalenesNeuroprotective Agents(3R)-((2,3-dihydro-5-methyl-3-((4-morpholinyl)methyl)pyrrolo-(1,2,3-de)-1,4-benzoxazin-6-yl)(1-naphthalenyl))methanoneBenzoxazinesCannabinoidsInterleukin-1 Receptor-Like 1 ProteinInterleukin-33Lectins, C-TypeMannose-Binding LectinsMannose ReceptorMorpholinesNaphthalenesNeuroprotective AgentsReceptors, CannabinoidReceptors, Cell SurfaceCarbon monoxide poisoningMicrogliaNeuroinflammationST2WIN 55,212-2

Identifiers

PMID31732924
OpenAlexW2983767727

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.