Introduction:
The Aryl hydrocarbon receptor (AhR) functions as a primary genomic defense mechanism against chemical exposure, balancing rapid detoxification with physiological homeostasis. However, persistent environmental ligands can shift the receptor from a protective sensor into a systemic disruptor, leading to severe toxicity. This study looks into the causes behind this transition by analyzing the structural and metabolic profiles of persistent dioxins, polycyclic aromatic hydrocarbons and transient dietary indoles to see how chemical persistence impacts the environment and human health.
Methods:
Physicochemical, pharmacokinetic, and comprehensive toxicological profiles, addressing both human and environmental ecotoxicity, were established using the ADMETlab 3.0, Deep-PK, and ProTox-3.0 platforms. Furthermore, blind molecular docking was executed via Pyrx against two high-resolution human AhR structures (8QMO and 7ZUB) to map binding affinities and core residue interactions within the PAS-B domain.
Results:
The results revealed a significant difference in risks attributed to chemical persistence. Industrial contaminants demonstrated outstanding lipid solubility, blood–brain barrier permeability, and considerable bioaccumulation potential. TCDD exhibited severe acute toxicity, but benzo[a]pyrene had strong predictive markers for carcinogenesis and endocrine disruption. In contrast, Indole-3-Carbinol demonstrated quick elimination, low aquatic toxicity, and a favorable safety profile. Molecular docking confirmed that all compounds bind to the AhR PAS-B pocket. Persistent pollutants, such as 3-MC and Benzo[a]pyrene, demonstrated the highest binding affinities, up to -14.4 kcal/mol, forming persistent complexes with important core residues.
Conclusions:
The metabolic stability of a ligand controls AhR-mediated biological effects. Because persistent pollutants resist metabolic breakdown, they bioaccumulate and maintain prolonged, high-affinity binding to the AhR. This sustained receptor activation, unlike the short-lived response of rapidly cleared dietary compounds, drives systemic toxicity. Overall, this research shows that integrating predictive ADME-Tox profiling with the molecular docking technique delivers a concrete in silico framework to accurately predict the bioaccumulation, receptor affinity, and health hazards of emerging environmental contaminants.
