Evidence map›Paper›PMID 30535411›Full record

ArticleToxicological sciences : an official journal of the Society of Toxicology2019

Generalized Concentration Addition Model Predicts Glucocorticoid Activity Bioassay Responses to Environmentally Detected Receptor-Ligand Mixtures.

Elizabeth Medlock Kakaley, Mary C Cardon, L Earl Gray, Phillip C Hartig, Vickie S Wilson

Open access · greenAbstract read
In one paragraph

Article in Toxicological sciences : an official journal of the Society of Toxicology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.6field-weighted citation impact, top 34% 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

9 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
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  5. Article
  6. A Comparative Multi-System Approach to Characterizing Bioactivity of Commonly Occurring Chemicals.International journal of environmental research and public health · 2022
    Article
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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

5 authors at 2 institutions in 1 country.

Elizabeth Medlock Kakaley*U.S. Environmental Protection Agency, Toxicity Assessment Division, Research Triangle Park, North Carolina 27711.
Mary C Cardon*U.S. Environmental Protection Agency, Toxicity Assessment Division, Research Triangle Park, North Carolina 27711.
L Earl Gray*U.S. Environmental Protection Agency, Toxicity Assessment Division, Research Triangle Park, North Carolina 27711.
Phillip C Hartig*U.S. Environmental Protection Agency, Toxicity Assessment Division, Research Triangle Park, North Carolina 27711.
Vickie S Wilson*U.S. Environmental Protection Agency, Toxicity Assessment Division, Research Triangle Park, North Carolina 27711.
Environmental Protection Agency · USUniversity of North Carolina at Chapel Hill · US

Funding

Intramural EPA EPA999999
6 · The paper itself

Abstract

Many glucocorticoid receptor (GR) agonists have been detected in waste and surface waters domestically and around the world, but the way a mixture of these environmental compounds may elicit a total glucocorticoid activity response in water samples remains unknown. Therefore, we characterized 19 GR ligands using a CV1 cell line transcriptional activation assay applicable to water quality monitoring. Cells were treated with individual GR ligands, a fixed ratio mixture of full or partial agonists, or a nonequipotent mixture with full and partial agonists. Efficacy varied (48.09%-102.5%) and potency ranged over several orders of magnitude (1.278 × 10-10 to 3.93 × 10-8 M). Concentration addition (CA) and response addition (RA) mixtures models accurately predicted equipotent mixture responses of full agonists (r2 = 0.992 and 0.987, respectively). However, CA and RA models assume mixture compounds produce full agonist-like responses, and therefore they overestimated observed maximal efficacies for mixtures containing partial agonists. The generalized concentration addition (GCA) model mathematically permits < 100% maximal responses, and fell within the 95% confidence interval bands of mixture responses containing partial agonists. The GCA, but not CA and RA, model predictions of nonequipotent mixtures containing both full and partial agonists fell within the same statistical distribution as the observed values, reinforcing the practicality of the GCA model as the best overall model for predicting GR activation. Elucidating the mechanistic basis of GR activation by mixtures of previously detected environmental GR ligands will benefit the interpretation of environmental sample contents in future water quality monitoring studies.

Indexed as

Models, BiologicalBiological AssayCorticosteroneDesoxycorticosteroneDexamethasoneDose-Response Relationship, DrugDrug Partial AgonismGlucocorticoidsLigandsPrednisoloneReceptors, GlucocorticoidTranscriptional ActivationCorticosteroneDesoxycorticosteroneDexamethasoneGlucocorticoidsLigandsPrednisoloneReceptors, Glucocorticoidbioassaychemical mixturesgeneralized concentration addition modelglucocorticoid receptorpartial agonist

Identifiers

PMID30535411
PMCPMC6709530
OpenAlexW2904440246

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.