Evidence map›Paper›PMID 30402721›Full record

ArticleDaru : journal of Faculty of Pharmacy, Tehran University of Medical Sciences2018

New mechanisms of phenytoin in calcium homeostasis: competitive inhibition of CD38 in hippocampal cells.

Leila Sadeghi, Reza Yekta, Gholamreza Dehghan

Abstract read
In one paragraph

Article in Daru : journal of Faculty of Pharmacy, Tehran University of Medical Sciences, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.1field-weighted citation impact, top 23% 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

3 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
  2. Article
  3. 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

3 authors at 1 institution in 1 country.

Leila SadeghiDepartment of Animal Biology, Faculty of Natural Sciences, University of Tabriz, P.O. Box 5166616471, Tabriz, Iran. l.sadeghi@tabrizu.ac.ir.ORCID http://orcid.org/0000-0003-1829-4388
Reza YektaDepartment of Animal Biology, Faculty of Natural Sciences, University of Tabriz, P.O. Box 5166616471, Tabriz, Iran.
Gholamreza DehghanDepartment of Animal Biology, Faculty of Natural Sciences, University of Tabriz, P.O. Box 5166616471, Tabriz, Iran.
University of Tabriz · IR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposePhenytoin is a major anticonvulsant drug that is effective to improve arrhythmia and neuropathic pain. According to early works, phenytoin affected cell membrane depolarization by sodium channel blocking, guanylyl and adenylyl cyclase suppression that cause to intracellular Na

methodsIn this study intracellular free Ca

resultsOur results confirmed phenytoin competitively inhibits cyclase activity of CD38 (IC

conclusionTaken together, one of the anticonvulsant mechanisms of phenytoin is Ca

Indexed as

ADP-ribosyl Cyclase 1AnimalsCalciumCatalytic DomainCell PolarityCells, CulturedCyclic ADP-RiboseDose-Response Relationship, DrugDown-RegulationGene Expression RegulationHippocampusHomeostasisMembrane GlycoproteinsMiceModels, MolecularMolecular Docking SimulationADP-ribosyl Cyclase 1CalciumCd38 protein, mouseCyclic ADP-RiboseMembrane GlycoproteinsPhenytoinCalcium homeostasisCD38Competitive inhibitionMembrane depolarizationPhenytoinSodium blocker

Identifiers

PMID30402721
PMCPMC6279657
OpenAlexW2899953310

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.