Herbicides and pesticides synergistically interact at low concentrations in complex mixtures

• Published in: Chemosphere (Oxford) 2024-04, Vol.353, p.141431-141431, Article 141431
• Main Authors: Alehashem, M., Peters, R., Fajana, H.O., Eslamizad, S., Hogan, N., Hecker, M., Siciliano, S.D.
• Format: Article
• Language: English
• Subjects: antagonism; Binary weight-of-evidence; cell lines; chlorinated hydrocarbons; Complex Mixtures - toxicity; Drug Interactions; exposure scenario; groundwater; Herbicides - toxicity; Humans; Interactions; land use; mechanism of action; Mixtures; Neuroblastoma; Pesticides; Pesticides - toxicity; polluted soils; risk; Risk assessment; risk characterization; synergism; toxicity testing; weight-of-evidence
• ISSN: 0045-6535; 1879-1298
• DOI: 10.1016/j.chemosphere.2024.141431

Assessing a complex mixture of pesticides at the impacted sites has been challenging for risk assessors for 50 years. The default assumption is that at low concentrations, pesticides interact additively with one another; thus, the risk posed by each component of a complex mixture could be simply added up. The EPA interaction-based hazard index (HIInteraction) modifies this assumption using a binary weight-of-evidence (BINWOE). However, data gaps often preclude HIInteraction use at most sites. This study evaluated these assumptions using the BINWOE to estimate the hazard index (HI) of select pesticide mixtures. The lack of in vivo binary interaction data led us to use a cell line, SH-SY5Y, to obtain the data necessary for the BINWOE approach. In the risk assessment, we considered the most active exposure scenario inhaling a mixture of volatile pesticides from contaminated soil and groundwater. The potential interactions between pesticides in 15 binary mixtures were investigated using the MTT assay in SH-SY5Y cells. Our findings showed that 60% of the binary mixtures elicited synergism (in at least one concentration), 27% displayed antagonism, and 13% showed additive effects in SH-SY5Y cells. Combining human safety data with in vitro interaction data indicated that adults and toddlers were at the highest risk when considering industrial and commercial land use, respectively, compared to other subpopulations. Incorporating interaction data into the risk assessment either increased the risk by up to 20% or decreased the risk by 2%, depending on the mixture. Our results demonstrate the predominant synergistic interactions, even at low concentrations, altered risk characterization at the complex operating site. Most concerning, organochlorine pesticides with the same mechanism of action did not follow dose additivity when evaluated by SH-SY5Y cell lines. Based on our observations, we caution that current HI methods based on additivity assumptions may underestimate the risk of organochlorine mixtures. [Display omitted] •The component-based risk assessment methods cannot adequately protect human health.•In vitro assays using human cells can create interaction data for risk assessment.•Pesticides with the same mechanism of action did not follow dose additivity in vitro.•The BINWOE approach can use in vitro interaction data to improve risk estimation.•Incorporating interaction data in risk assessment increased the risk of nine mixtures.