Evidence map›Paper›PMID 33389386›Full record

ArticleNeurochemical research2021

Suppression of TLR4/MyD88/TAK1/NF-κB/COX-2 Signaling Pathway in the Central Nervous System by Bexarotene, a Selective RXR Agonist, Prevents Hyperalgesia in the Lipopolysaccharide-Induced Pain Mouse Model.

Sefika Pinar Senol, Meryem Temiz-Resitoglu, Demet Sinem Guden, Ayse Nihal Sari, Seyhan Sahan-Firat, Bahar Tunctan

Abstract read
PubMed Publisher
In one paragraph

Article in Neurochemical research, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 1 pooled it
1.7field-weighted citation impact, top 17% 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

12 citing papers in PubMed, 1 synthesis or guideline pooled it, 18 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Review
  5. Article
  6. Review
  7. Article
  8. Article
  9. Suppressive Effect of Tetrahydrocurcumin onOxidative medicine and cellular longevity · 2022
    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

6 authors at 1 institution in 1 country.

Sefika Pinar SenolDepartment of Pharmacology, Faculty of Pharmacy, Mersin University, Mersin, Turkey.
Meryem Temiz-ResitogluDepartment of Pharmacology, Faculty of Pharmacy, Mersin University, Mersin, Turkey.
Demet Sinem GudenDepartment of Pharmacology, Faculty of Pharmacy, Mersin University, Mersin, Turkey.
Ayse Nihal SariDepartment of Pharmacology, Faculty of Pharmacy, Mersin University, Mersin, Turkey.
Seyhan Sahan-FiratDepartment of Pharmacology, Faculty of Pharmacy, Mersin University, Mersin, Turkey.
Bahar TunctanDepartment of Pharmacology, Faculty of Pharmacy, Mersin University, Mersin, Turkey. btunctan@gmail.com.ORCID http://orcid.org/0000-0003-3439-7803
Mersin Üniversitesi · TR

Funding

Mersin Üniversitesi 2018-1-TP3-2814Türkiye Bilimsel ve Teknolojik Araştirma Kurumu SBAG-217S235
6 · The paper itself

Abstract

A selective RXR agonist, bexarotene, has been shown to have anti-inflammatory, anti-nociceptive, and neuroprotective effects in several models of numerous neurological diseases characterized by systemic inflammation. The mechanisms underlying these effects remains unknown. To elucidate these mechanisms, we investigated whether the TLR4/MyD88/TAK1/NF-κB/COX-2 signaling pathway in the CNS mediates the effect of bexarotene to prevent hyperalgesia in the LPS-induced inflammatory pain mouse model. The reaction time to thermal stimuli within 30 s was evaluated by the hot plate test in male mice treated with saline, LPS (10 mg/kg), DMSO, and/or bexarotene (0.1, 1, 3, or 10 mg/kg) after 6 h. The latency to the thermal stimulus (18.11 ± 1.36 s) in the LPS-treated mice was significantly decreased by 30% compared with saline-treated mice (25.84 ± 1.99 s). Treatment with bexarotene only at a dose of 10 mg/kg showed a significant increase in the latency by 22.49 ± 1.00 s compared with LPS-treated mice. Bexarotene also prevented the reduction in RXRα protein expression associated with a rise in the expression of TLR4, MyD88, phosphorylated TAK1, NF-κB p65, phosphorylated NF-κB p65, COX-2, and IL-1β proteins, in addition to COX-2 activity and levels of PGE

Indexed as

AnalgesicsAnimalsAnti-Inflammatory AgentsBexaroteneCyclooxygenase 2HyperalgesiaLipopolysaccharidesMaleMAP Kinase Kinase Kinase 7MAP Kinase Kinase KinasesMiceMice, Inbred BALB CMyeloid Differentiation Factor 88NF-kappa B p50 SubunitRetinoid X ReceptorsSignal TransductionAnalgesicsAnti-Inflammatory AgentsBexaroteneCyclooxygenase 2LipopolysaccharidesMAP Kinase Kinase Kinase 7MAP Kinase Kinase KinasesMyd88 protein, mouseMyeloid Differentiation Factor 88NF-kappa B p50 SubunitNfkb1 protein, mousePtgs2 protein, mouseRetinoid X ReceptorsTlr4 protein, mouseToll-Like Receptor 4BexaroteneInflammatory hyperalgesiaLipopolysaccharideMiceRXRTLR4/MyD88/TAK1/NF-κB/COX-2

Identifiers

PMID33389386
OpenAlexW3120448045

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.