4.5 Article

Synergistic Interaction of Polycyclic Aromatic Hydrocarbons, Phthalate Esters, or Phenol on DNA Adduct Formation by Aristolochic Acid I: Insights into the Etiology of Balkan Endemic Nephropathy

Journal

CHEMICAL RESEARCH IN TOXICOLOGY
Volume 35, Issue 5, Pages 849-857

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.chemrestox.2c00026

Keywords

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Funding

  1. Hong Kong Research Grants Council [GRF 16302918]

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This study investigates the effects of coexposure to phthalate esters, lignite coal-derived phenol, and polycyclic aromatic hydrocarbons (PAHs) on the metabolism and DNA adduct formation of aristolochic acid I (AAI), aiming to understand the etiological mechanism of Balkan endemic nephropathy (BEN). The results show that the presence of environmental pollutants affects the activation and DNA adduct formation of AAI. Thus, this study contributes to a better understanding of the etiology of BEN and provides insights for risk reduction strategies.
Balkan endemic nephropathy (BEN) is a multifactorial environmental disease, with chronic exposure to aristolochic acids (AAs) through AA-contaminated food being one of the major etiological mechanisms. However, the bulk of previous research has only focused on investigating the possible roles of individual pollutants in disease development and the etiological mechanism of BEN remains controversial. In this study, we investigated the exposure concentration and duration dependence of coexposure to phthalate esters and lignite coal-derived phenol and polycyclic aromatic hydrocarbons (PAHs) on the metabolism and DNA adduct formation of aristolochic acid I (AAI). Results showed that both the metabolic activation and DNA adduct formation of AAI in cultured human kidney cells were affected by their coexposure to the above-mentioned environmental pollutants. Furthermore, our results suggest that chemicals leached from lignite coal likely played a role by triggering AA-activating enzymes to produce more of the promutagenic DNA adducts, thus further elevating the nephrotoxicity and carcinogenicity of AAs and increasing the risk of BEN. It is believed that the results of this study provide a better understanding of the etiological mechanism of BEN and offer insights into methods and policies to lower the risk of this devastating disease.

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