A Comparison of In Vitro Metabolic Clearance of Various Regulatory Fish Species Using Hepatic S9 Fractions. 2024

Megan Zercher, and Jason A Coral, and Diane Nabb, and Griselda Powers, and Alan Jones, and Karla Johanning
FMC Agricultural Solutions, Newark, Delaware, USA.

Bioaccumulation predictions can be substantially improved by combining in vitro metabolic rate measurements derived from rainbow trout hepatocytes and/or hepatic S9 fractions with quantitative structure-activity relationship (QSAR) modeling approaches. Compared with in vivo testing guidelines Organisation for Economic Co-operation and Development (OECD) 305 and Office of Chemical Safety and Pollution Prevention (OCSPP; an office of the US Environmental Protection Agency) 850.1730, the recently adopted OECD test guidelines 319A and 319B are in vitro approaches that have the potential to provide a time- and cost-efficient, humane solution, reducing animal use while addressing uncertainties in bioaccumulation across species. The present study compares the hepatic clearance of the S9 subcellular fraction of rainbow trout, bluegill, common carp, fathead minnow, and largemouth bass, discerning potential differences in metabolism between different warm- and cold-water species. With refinements to the in vitro metabolic S9 assay for high-throughput analysis, we measured in vitro clearance rates of seven chemicals crossing multiple classes of chemistry and modes of action. We confirmed that data from rainbow trout liver S9 fraction metabolic rates can be utilized to predict rainbow trout bioconcentration factors using an in vitro to in vivo extrapolation model, as intended in the OECD 319B applicability domain per the bioaccumulation prediction. Also, we determined that OECD 319B can be applied to other species, modified according to their habitat, adaptations to feeding behavior, and environmental conditions (e.g., temperature). Once toxicokinetics for each species is better understood and appropriate models are developed, this method can be an excellent tool to determine hepatic clearance and potential bioaccumulation across species. The present study could be leveraged prior to or in place of initiating in vivo bioconcentration studies, thus optimizing selection of appropriate fish species. Environ Toxicol Chem 2024;00:1-16. © 2024 SETAC.

UI MeSH Term Description Entries

Related Publications

Megan Zercher, and Jason A Coral, and Diane Nabb, and Griselda Powers, and Alan Jones, and Karla Johanning
February 2017, Environmental toxicology and chemistry,
Megan Zercher, and Jason A Coral, and Diane Nabb, and Griselda Powers, and Alan Jones, and Karla Johanning
June 2020, Molecules (Basel, Switzerland),
Megan Zercher, and Jason A Coral, and Diane Nabb, and Griselda Powers, and Alan Jones, and Karla Johanning
October 1985, Mutation research,
Megan Zercher, and Jason A Coral, and Diane Nabb, and Griselda Powers, and Alan Jones, and Karla Johanning
December 2013, Toxicological sciences : an official journal of the Society of Toxicology,
Megan Zercher, and Jason A Coral, and Diane Nabb, and Griselda Powers, and Alan Jones, and Karla Johanning
January 2006, In vitro cellular & developmental biology. Animal,
Megan Zercher, and Jason A Coral, and Diane Nabb, and Griselda Powers, and Alan Jones, and Karla Johanning
January 2017, PloS one,
Megan Zercher, and Jason A Coral, and Diane Nabb, and Griselda Powers, and Alan Jones, and Karla Johanning
February 2017, Yao xue xue bao = Acta pharmaceutica Sinica,
Megan Zercher, and Jason A Coral, and Diane Nabb, and Griselda Powers, and Alan Jones, and Karla Johanning
December 2015, Environmental toxicology and chemistry,
Megan Zercher, and Jason A Coral, and Diane Nabb, and Griselda Powers, and Alan Jones, and Karla Johanning
September 2019, Journal of pharmaceutical and biomedical analysis,
Megan Zercher, and Jason A Coral, and Diane Nabb, and Griselda Powers, and Alan Jones, and Karla Johanning
January 2008, Drug metabolism and drug interactions,
Copied contents to your clipboard!