Evidence map›Paper›PMID 36351837›Full record

ReviewDrug metabolism and disposition: the biological fate of chemicals2023

Phenobarbital in Nuclear Receptor Activation: An Update.

Shuaiqian Men, Hongbing Wang

Open access · greenAbstract readReview
In one paragraph

Review in Drug metabolism and disposition: the biological fate of chemicals, 2023. 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
2.1field-weighted citation impact, top 14% 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, 13 citations in OpenAlex.

  1. ToxCompl completion of the DrugMatrix toxicogenomics database: an integrated resource for hypothesis generation.Toxicological sciences : an official journal of the Society of Toxicology · 2026
    Article
  2. Article
  3. Article
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  5. 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

2 authors at 1 institution in 1 country.

Shuaiqian MenDepartment of Pharmaceutical Sciences, University of Maryland School of Pharmacy, Baltimore, Maryland (S.M., H.W.).
Hongbing WangDepartment of Pharmaceutical Sciences, University of Maryland School of Pharmacy, Baltimore, Maryland (S.M., H.W.) hongbing.wang@rx.umaryland.edu.ORCID 0000-0002-6224-6888
University of Maryland, Baltimore · US

Funding

Novel noncanonical actions of CAR in human LiverR01CA262084 · NCI · UNIVERSITY OF MARYLAND BALTIMORE · PI WANG, HONGBING · 2021 to 2025
$2.0M
Function and Regulation of SLC13A5 in the LiverR01GM121550 · NIGMS · UNIVERSITY OF MARYLAND BALTIMORE · PI WANG, HONGBING · 2018 to 2021
$1.3M
Human CYP2B6 in alcohol metabolism and alcoholic liver injuryR21AA028521 · NIAAA · UNIVERSITY OF MARYLAND BALTIMORE · PI WANG, HONGBING · 2020 to 2021
$406k
NCI NIH HHS R01 CA262084NIAAA NIH HHS R21 AA028521NIGMS NIH HHS R01 GM121550
6 · The paper itself

Abstract

Phenobarbital (PB) is a commonly prescribed anti-epileptic drug that can also benefit newborns from hyperbilirubinemia. Being the first drug demonstrating hepatic induction of cytochrome P450 (CYP), PB has since been broadly used as a model compound to study xenobiotic-induced drug metabolism and clearance. Mechanistically, PB-mediated CYP induction is linked to a number of nuclear receptors, such as the constitutive androstane receptor (CAR), pregnane X receptor (PXR), and estrogen receptor

Indexed as

Receptors, SteroidAnimalsCytochrome P-450 Enzyme SystemHumansInfant, NewbornLiverPhenobarbitalReceptors, Cytoplasmic and NuclearXenobioticsCytochrome P-450 Enzyme SystemPhenobarbitalReceptors, Cytoplasmic and NuclearReceptors, SteroidXenobiotics

Identifiers

PMID36351837
PMCPMC9900862
OpenAlexW4308678759

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.