Upregulation of fatty acid synthesis genes in the livers of adolescent female rats caused by inhalation exposure to PCB52 (2,2′,5,5′-Tetrachlorobiphenyl)

IF 4.2 3区 环境科学与生态学 Q2 ENVIRONMENTAL SCIENCES
Brynn Kyleakin Helm-Kwasny , Amanda Bullert , Hui Wang , Michael S. Chimenti , Andrea Adamcakova-Dodd , Xuefang Jing , Xueshu Li , David K. Meyerholz , Peter S. Thorne , Hans-Joachim Lehmler , James A. Ankrum , Aloysius J. Klingelhutz
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引用次数: 0

Abstract

Elevated airborne PCB levels in older schools are concerning due to their health impacts, including cancer, metabolic dysfunction-associated steatotic liver disease (MASLD), cardiovascular issues, neurodevelopmental diseases, and diabetes. During a four-week inhalation exposure to PCB52, an air pollutant commonly found in school environments, adolescent rats exhibited notable presence of PCB52 and its hydroxylated forms in their livers, alongside changes in gene expression. Female rats exhibited more pronounced changes in gene expression compared to males, particularly in fatty acid synthesis genes regulated by the transcription factor SREBP1. In vitro studies with human liver cells showed that the hydroxylated metabolite of PCB52, 4-OH-PCB52, but not the parent compound, upregulated genes involved in fatty acid biosynthesis similar to in vivo exposure. These findings highlight the sex-specific effects of PCB52 exposure on livers, particularly in females, suggesting a potential pathway for increased MASLD susceptibility.

吸入 PCB52(2,2',5,5'- 四氯联苯)导致青春期雌性大鼠肝脏中脂肪酸合成基因的上调。
老式学校空气中多氯联苯含量的升高令人担忧,因为它会影响健康,包括癌症、代谢功能障碍相关性脂肪肝(MASLD)、心血管问题、神经发育疾病和糖尿病。在对学校环境中常见的空气污染物多氯联苯-52 进行为期四周的吸入接触后,青少年大鼠的肝脏中明显出现了多氯联苯-52 及其羟化形式,同时基因表达也发生了变化。与雄性大鼠相比,雌性大鼠的基因表达发生了更明显的变化,特别是受转录因子 SREBP1 调节的脂肪酸合成基因。用人肝细胞进行的体外研究表明,多氯联苯-52 的羟基化代谢物 4-OH-PCB52 会上调参与脂肪酸生物合成的基因,而母体化合物则不会。这些发现凸显了接触 PCB52 对肝脏(尤其是女性肝脏)产生的性别特异性影响,表明这是增加 MASLD 易感性的潜在途径。
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来源期刊
CiteScore
7.00
自引率
4.70%
发文量
185
审稿时长
34 days
期刊介绍: Environmental Toxicology and Pharmacology publishes the results of studies concerning toxic and pharmacological effects of (human and veterinary) drugs and of environmental contaminants in animals and man. Areas of special interest are: molecular mechanisms of toxicity, biotransformation and toxicokinetics (including toxicokinetic modelling), molecular, biochemical and physiological mechanisms explaining differences in sensitivity between species and individuals, the characterisation of pathophysiological models and mechanisms involved in the development of effects and the identification of biological markers that can be used to study exposure and effects in man and animals. In addition to full length papers, short communications, full-length reviews and mini-reviews, Environmental Toxicology and Pharmacology will publish in depth assessments of special problem areas. The latter publications may exceed the length of a full length paper three to fourfold. A basic requirement is that the assessments are made under the auspices of international groups of leading experts in the fields concerned. The information examined may either consist of data that were already published, or of new data that were obtained within the framework of collaborative research programmes. Provision is also made for the acceptance of minireviews on (classes of) compounds, toxicities or mechanisms, debating recent advances in rapidly developing fields that fall within the scope of the journal.
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