Evidence map›Paper›PMID 33597883›Full record

ArticleFrontiers in pharmacology2020

Analgesic and Anti-Inflammatory Effects of Perampanel in Acute and Chronic Pain Models in Mice: Interaction With the Cannabinergic System.

Carmen De Caro, Claudia Cristiano, Carmen Avagliano, Mariarosaria Cuozzo, Giovanna La Rana, Gabriella Aviello, Giovambattista De Sarro, Antonio Calignano, Emilio Russo, Roberto Russo

Open access · goldAbstract read
In one paragraph

Article in Frontiers in pharmacology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
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, 16 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Neuropathic pain: Mechanisms and therapeutic strategies.Frontiers in cell and developmental biology · 2023
    Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Facile synthesis of 6-organyl-4-(trifluoromethyl)pyridin-2(1Russian chemical bulletin = Izvestiia Akademii nauk. Seriia khimicheskaia · 2022
    Article
  11. Article
  12. 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

10 authors at 1 institution in 1 country.

Carmen De CaroDepartment of Health Sciences, School of Medicine, University of Catanzaro, Catanzaro, Italy.
Claudia CristianoDepartment of Pharmacy, University of Naples Federico II, Naples, Italy.
Carmen AvaglianoDepartment of Pharmacy, University of Naples Federico II, Naples, Italy.
Mariarosaria CuozzoDepartment of Pharmacy, University of Naples Federico II, Naples, Italy.
Giovanna La RanaDepartment of Pharmacy, University of Naples Federico II, Naples, Italy.
Gabriella AvielloDepartment of Pharmacy, University of Naples Federico II, Naples, Italy.
Giovambattista De SarroDepartment of Health Sciences, School of Medicine, University of Catanzaro, Catanzaro, Italy.
Antonio CalignanoDepartment of Pharmacy, University of Naples Federico II, Naples, Italy.
Emilio RussoDepartment of Health Sciences, School of Medicine, University of Catanzaro, Catanzaro, Italy.
Roberto RussoDepartment of Pharmacy, University of Naples Federico II, Naples, Italy.
University of Naples Federico II · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pain conditions, such as neuropathic pain (NP) and persistent inflammatory pain are therapeutically difficult to manage. Previous studies have shown the involvement of glutamate receptor in pain modulation and in particular same of these showed the key role of the AMPA ionotropic glutamate receptor subtype. Antiseizure medications (ASMs) are often used to treat this symptom, however the effect of perampanel (PER), an ASM acting as selective, non-competitive inhibitor of the AMPA receptor on the management of pain has not well been investigated yet. Here we tested the potential analgesic and anti-inflammatory effects of PER, in acute and chronic pain models. PER was given orally either in acute (5 mg/kg) or repeated administration (3 mg/kg/d for 4 days). Pain response was assessed using models of nociceptive sensitivity, visceral and inflammatory pain, and mechanical allodynia and hyperalgesia induced by chronic constriction injury to the sciatic nerve. PER significantly reduced pain perception in all behavioral tests as well as CCI-induced mechanical allodynia and hyperalgesia in acute regimen (5 mg/kg). This effect was also observed after repeated treatment using the dose of 3 mg/kg/d. The antinociceptive, antiallodynic and antihyperalgesic effects of PER were attenuated when the CB

Indexed as

AMPA receptorCB1 receptorinflammationpainperampanel

Identifiers

PMID33597883
PMCPMC7883473
OpenAlexW3128152313

What OpenQuestion holds

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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.