Evidence map›Paper›PMID 31540101›Full record

ArticleInternational journal of molecular sciences2019

Sesquiterpenes Are Agonists of the Pregnane X Receptor but Do Not Induce the Expression of Phase I Drug-Metabolizing Enzymes in the Human Liver.

Michaela Šadibolová, Tomáš Zárybnický, Tomáš Smutný, Petr Pávek, Zdeněk Šubrt, Petra Matoušková, Lenka Skálová, Iva Boušová

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2019. 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
0.4field-weighted citation impact, top 33% 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, 4 citations in OpenAlex.

  1. Review
  2. Analgesic Potential of Terpenes Derived fromPharmacological reviews · 2021
    Review
  3. 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

8 authors at 1 institution in 1 country.

Michaela ŠadibolováDepartment of Biochemical Sciences, Faculty of Pharmacy in Hradec Králové, Charles University, 500 05 Hradec Králové, Czech Republic.
Tomáš ZárybnickýDepartment of Biochemical Sciences, Faculty of Pharmacy in Hradec Králové, Charles University, 500 05 Hradec Králové, Czech Republic. zarybnto@faf.cuni.cz.ORCID 0000-0001-6402-9708
Tomáš SmutnýDepartment of Pharmacology and Toxicology, Faculty of Pharmacy in Hradec Králové, Charles University, 500 05 Hradec Králové, Czech Republic. smutt6aa@faf.cuni.cz.
Petr PávekDepartment of Pharmacology and Toxicology, Faculty of Pharmacy in Hradec Králové, Charles University, 500 05 Hradec Králové, Czech Republic. pavek@faf.cuni.cz.
Zdeněk ŠubrtDepartment of General Surgery, Third Faculty of Medicine and University Hospital Královské Vinohrady, Charles University, 100 34 Prague, Czech Republic. subrt@email.cz.
Petra MatouškováDepartment of Biochemical Sciences, Faculty of Pharmacy in Hradec Králové, Charles University, 500 05 Hradec Králové, Czech Republic. matousp7@faf.cuni.cz.ORCID 0000-0002-9421-5744
Lenka SkálováDepartment of Biochemical Sciences, Faculty of Pharmacy in Hradec Králové, Charles University, 500 05 Hradec Králové, Czech Republic. skaloval@faf.cuni.cz.
Iva BoušováDepartment of Biochemical Sciences, Faculty of Pharmacy in Hradec Králové, Charles University, 500 05 Hradec Králové, Czech Republic. Iva.Bousova@faf.cuni.cz.ORCID 0000-0003-2863-717X
Charles University · CZ

Funding

Grantová Agentura České Republiky 18-09946SMinisterstvo Školství, Mládeže a Tělovýchovy CZ.02.1.01/0.0/0.0/16_019/0000841Univerzita Karlova v Praze SVV 260 416
6 · The paper itself

Abstract

Sesquiterpenes, the main components of plant essential oils, are bioactive compounds with numerous health-beneficial activities. Sesquiterpenes can interact with concomitantly administered drugs due to the modulation of drug-metabolizing enzymes (DMEs). The aim of this study was to evaluate the modulatory effects of six sesquiterpenes (farnesol,

Indexed as

AgedAged, 80 and overAldo-Keto ReductasesCarbonyl Reductase (NADPH)Cytochrome P-450 CYP3ACytochrome P-450 Enzyme SystemCytochrome P450 Family 2FarnesolFemaleHepatocytesHep G2 CellsHumansLiverMaleMetabolic Clearance RateMiddle AgedAldo-Keto ReductasesCarbonyl Reductase (NADPH)caryophyllenecaryophyllene oxidecytochrome P-450 CYP2C subfamilyCytochrome P-450 CYP3ACytochrome P-450 Enzyme SystemCytochrome P450 Family 2FarnesolhumuleneMonocyclic SesquiterpenesnerolidolPolycyclic SesquiterpenesPregnane X ReceptorReceptors, Aryl HydrocarbonRNA, MessengerSesquiterpenescytochrome P450 3A4gene reporter assaymRNA expressionprecision-cut liver slicespregnane X receptorprotein expressionsesquiterpene

Identifiers

PMID31540101
PMCPMC6769599
OpenAlexW2972494452

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.