4.7 Article

Chemical Mixtures in Household Environments: In Silico Predictions and In Vitro Testing of Potential Joint Action on PPAR gamma in Human Liver Cells

Journal

TOXICS
Volume 10, Issue 5, Pages -

Publisher

MDPI
DOI: 10.3390/toxics10050199

Keywords

mixtures; in vitro; toxicology; in silico

Funding

  1. National Institutes of Health (NIH), from the National Institute of Environmental Health Sciences
  2. Institute for Environmental Health Solutions at the University of North Carolina Gillings School of Global Public Health
  3. [P42ES031007]

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This study used in silico methods to identify common chemicals co-occurring in household environments that may have joint effects on PPAR gamma. Testing five commonly co-occurring chemicals in human liver cells showed that mixtures had a more significant impact on PPAR gamma and INSR expression. Future studies will further quantify these joint effects at various doses to prioritize chemical combinations.
There are thousands of chemicals that humans can be exposed to in their everyday environments, the majority of which are currently understudied and lack substantial testing for potential exposure and toxicity. This study aimed to implement in silico methods to characterize the chemicals that co-occur across chemical and product uses in our everyday household environments that also target a common molecular mediator, thus representing understudied mixtures that may exacerbate toxicity in humans. To detail, the Chemical and Products Database (CPDat) was queried to identify which chemicals co-occur across common exposure sources. Chemicals were preselected to include those that target an important mediator of cell health and toxicity, the peroxisome proliferator activated receptor gamma (PPAR gamma), in liver cells that were identified through query of the ToxCast/Tox21 database. These co-occurring chemicals were thus hypothesized to exert potential joint effects on PPAR gamma. To test this hypothesis, five commonly co-occurring chemicals (namely, benzyl cinnamate, butyl paraben, decanoic acid, eugenol, and sodium dodecyl sulfate) were tested individually and in combination for changes in the expression of PPAR gamma and its downstream target, insulin receptor (INSR), in human liver HepG2 cells. Results showed that these likely co-occurring chemicals in household environments increased both PPAR gamma and INSR expression more significantly when the exposures occurred as mixtures vs. as individual chemicals. Future studies will evaluate such chemical combinations across more doses, allowing for further quantification of the types of joint action while leveraging this method of chemical combination prioritization. This study demonstrates the utility of in silico-based methods to identify chemicals that co-occur in the environment for mixtures toxicity testing and highlights relationships between understudied chemicals and changes in PPAR gamma-associated signaling.

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