Data from: Mitochondrial dysfunction and oxidative stress contribute to cross-generational toxicity of benzo(a)pyrene in Danio rerio.

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Authors: Nishad Jayasundara, Ellen D. Cooper, Richard T. Di Giulio, Joel N. Meyer, Anthony N. Oliveri, Andrey Massarsky, Casey D. Lindberg, Edward D. Levin, Jordan S. Kozal
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Abstract

The potential for polycyclic aromatic hydrocarbons (PAHs) to have adverse effects that persist across generations is an emerging concern for human and wildlife health. This study evaluated the role of mitochondria, which are maternally inherited, in the cross-generational toxicity of benzo(a)pyrene (BaP), a model PAH and known mitochondrial toxicant. Mature female zebrafish (F0) were fed diets containing 0, 12.5, 125, or 1250 μg BaP/g at a feed rate of 1% body weight twice/day for 21 days. These females were bred with unexposed males, and the embryos (F1) were collected for subsequent analyses. Data herein include mitochondrial function of organs ex vivo (brain, heart, liver, and ovary) from exposed adults as well as mitochondrial function raw data and profiles for their F1 embryos.

Fields of Study & Subjects

Toxic Organic Pollutants Impact Environmental Toxicology and Ecotoxicology Reproductive biology and impacts on aquatic species

Publication details

Journal / source
Research Data Repository, Duke University
Publication date
16 February 2026
Language
EN
Document type
Dataset