Evidence map›Paper›PMID 42794617›Full record

ArticleInternational journal of molecular sciences2026

A Universal Plasticizer Alkylsulfonic Phenyl Ester Activates Pregnane X Receptor to Increase Intestinal Cholesterol Uptake.

Nnamdi Okore, Wangeci Kariuki, Conner Brown, Michael A Moxley, Naara Ramirez, Yipeng Sui

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Nnamdi OkoreDepartment of Biology, University of Nebraska at Kearney, Kearney, NE 68849, USA.
Wangeci KariukiDepartment of Biology, University of Nebraska at Kearney, Kearney, NE 68849, USA.
Conner BrownDepartment of Biology, University of Nebraska at Kearney, Kearney, NE 68849, USA.
Michael A MoxleyDepartment of Chemistry, University of Nebraska at Kearney, Kearney, NE 68849, USA.
Naara RamirezDepartment of Biology, University of Nebraska at Kearney, Kearney, NE 68849, USA.
Yipeng SuiDepartment of Biology, University of Nebraska at Kearney, Kearney, NE 68849, USA.

Funding

UNMC Structural Biology CoreP20GM103427 · NIGMS · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI Heather Colleen Jensen-Smith · 2012 to 2026
$59.2M
The Potential Effects of a Universal Plasticizer Alkylsulfonic Phenyl Ester on Dyslipidemia and AtherosclerosisR16GM159691 · NIGMS · UNIVERSITY OF NEBRASKA KEARNEY · PI Yipeng Sui · 2026 to 2026
$133k
NIGMS NIH HHS P20 GM103427NIGMS NIH HHS P20GM103427NIGMS NIH HHS R16 GM159691NIGMS NIH HHS R16GM159691
6 · The paper itself

Abstract

Alkylsulfonic phenyl ester (ASE) is an alternate non-phthalate plasticizer used in PVC and polyurethane manufacture, such as for medical tubing and toys. Plastic-associated endocrine disrupting chemicals have been associated with increased cardiovascular disease risks and have been established as the agonists of a xenobiotic sensor, pregnane X receptor (PXR), which has atherogenic and dyslipidemic effects. However, it is unknown whether ASE activates PXR to adversely affect cardiovascular system. Our objective is to investigate how ASE impacts lipid profiles and cholesterol uptake via PXR signaling. Human hepatic and intestinal cells were used to test activation of PXR by ASE. The computational docking study and site-directed mutagenesis were used to identify key amino acid residues in PXR that interacted with ASE. The natural PXR inhibitor resveratrol was used to prohibit PXR activities. The male C57BL/6 wildtype mice were fed with ASE to evaluate if ASE could alter plasma lipid levels. Our data suggested that ASE was a specific PXR agonist and increased atherogenic cholesterol levels in mice mediated by PXR. Furthermore, ASE treatment increased cholesterol uptake by human intestinal cells through PXR signaling. Our study elucidates the role of PXR as a mediator of xenobiotic-elicited dyslipidemia and provides evidence for the future risk assessment of ASE on cardiovascular diseases.

Indexed as

AlkanesulfonatesCholesterolIntestinal MucosaPlasticizersPregnane X ReceptorAnimalsHumansIntestinesMaleMiceMice, Inbred C57BLMolecular Docking SimulationSignal TransductionAlkanesulfonatesCholesterolPlasticizersPregnane X Receptoralkylsulfonic phenyl estercardiovascular diseasecholesterol uptakedyslipidemiaendocrine disrupting chemicalpregnane X receptor

Identifiers

PMID42794617
PMCPMC13607809

What Socratic 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 Socratic graph.