4.5 Article

Transgenerational effects of polychlorinated biphenyls: 2. Hypothalamic gene expression in rats

Journal

BIOLOGY OF REPRODUCTION
Volume 105, Issue 3, Pages 690-704

Publisher

OXFORD UNIV PRESS INC
DOI: 10.1093/biolre/ioab066

Keywords

anteroventral periventricular nucleus; arcuate nucleus; Aroclor 1221 (A1221); estrogen; endocrine-disrupting chemical; hypothalamus; neuroendocrine; polychlorinated biphenyls; sex difference; transgenerational

Funding

  1. NIH (NIEHS) [RO1 ES023254, RO1 ES029464]

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Exposure to polychlorinated biphenyls (PCBs) during pregnancy can lead to unique gene expression profiles in the hypothalamus across three generations in a sex- and lineage-dependent manner. Results vary between generations and are influenced by lineage, indicating that the legacy of PCBs continues for multiple generations.
Polychlorinated biphenyls (PCBs) are endocrine-disrupting chemicals (EDCs) with well-established effects on reproduction and behavior in developmentally-exposed (F1) individuals. Because of evidence for transgenerational effects of EDCs on the neuroendocrine control of reproductive physiology, we tested the hypothesis that prenatal PCB exposure leads to unique hypothalamic gene-expression profiles in three generations. Pregnant Sprague-Dawley rats were treated on gestational days 16 and 18 with the PCB mixture Aroclor 1221 (A1221), vehicle (3% DMSO in sesame oil), or estradiol benzoate (EB, 50 mu g/kg), the latter a positive control for estrogenic effects of A1221. Maternal- and paternal-lineage F2 and F3 generations were bred using untreated partners. The anteroventral periventricular nucleus (AVPV) and arcuate nucleus (ARC), involved in the hypothalamic control of reproduction, were dissected from F1 to F3 females and males, RNA extracted, and gene expression measured in a qPCR array. We detected unique gene-expression profiles in each generation, which were sex- and lineage-specific. In the AVPV, treatment significantly changed 10, 25, and 11 transcripts in F1, F2, and F3 generations, whereas 10, 1, and 12 transcripts were changed in these generations in the ARC. In the F1 AVPV and ARC, most affected transcripts were decreased by A1221. In the F2 AVPV, most effects of A1221 were observed in females of the maternal lineage, whereas only Pomc expression changed in the F2 ARC (by EB). The F3 AVPV and ARC were mainly affected by EB. It is notable that results in one generation do not predict results in another, and that lineage was a major determinant in results. Thus, transient prenatal exposure of F1 rats to A1221 or EB can alter hypothalamic gene expression across three generations in a sex- and lineage-dependent manner, leading to the conclusion that the legacy of PCBs continues for generations. [GRAPHICS] .

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