Department of Pharmacology, College of Graduate Studies, Midwestern University, Downers Grove, IL 60515, USA.
Chicago College of Osteopathic Medicine, Midwestern University, Downers Grove, IL 60515, USA.
Endocrinology. 2021 Nov 1;162(11). doi: 10.1210/endocr/bqab160.
Polybrominated diphenyl ethers (PBDEs) have been previously shown to alter various endocrine biosynthetic pathways. Growing epidemiological evidence suggests that PBDEs alter cardiovascular function. The goal of this study was to examine the effects of BDE-47 on adrenal corticosteroid pathways that play vital roles in cardiovascular homeostasis and pathophysiology. The effect of BDE-47 on aldosterone and cortisol secretion was characterized in a human adrenocortical cell line. HAC15 cells were exposed to various concentrations of BDE-47 (1 nM to 100 μM). Cell viability, corticosteroid secretion, gene expression of enzymes involved in corticosteroid synthesis, and metabolic activity was examined. Additionally, Sprague Dawley male rats were orally exposed to BDE-47 (10 or 100 µg/kg), 5 days per week for 16 weeks. Organ weights and plasma corticosteroid levels were measured. In HAC15 cells, basal and stimulated aldosterone and cortisol secretion was significantly increased by BDE-47. Gene expression of several enzymes involved in corticosteroid synthesis and mitochondrial metabolism also increased. In Sprague Dawley rats, adrenal but not heart, kidney, or liver weights, were significantly increased in BDE-47 treatment groups. Plasma corticosterone levels were significantly increased in the 100 µg BDE-47/kg treatment group. No change in plasma aldosterone levels were observed with BDE-47 exposure. These data indicate that BDE-47 disrupts the regulation of corticosteroid secretion and provides further evidence that PBDEs are potential endocrine disruptors. Future studies will determine the underlying molecular mechanism of altered corticosteroid production and examine whether these alterations result in underlying cardiovascular disease in our rodent model of 16-week BDE-47 exposure.
多溴联苯醚 (PBDEs) 先前已被证明会改变各种内分泌生物合成途径。越来越多的流行病学证据表明,PBDEs 会改变心血管功能。本研究的目的是研究 BDE-47 对肾上腺皮质类固醇途径的影响,这些途径在心血管稳态和病理生理学中起着至关重要的作用。在人肾上腺皮质细胞系中研究了 BDE-47 对醛固酮和皮质醇分泌的影响。将 HAC15 细胞暴露于不同浓度的 BDE-47(1 nM 至 100 μM)。检查了细胞活力、皮质类固醇分泌、参与皮质类固醇合成的酶的基因表达和代谢活性。此外,还将 Sprague Dawley 雄性大鼠经口暴露于 BDE-47(10 或 100μg/kg),每周 5 天,共 16 周。测量器官重量和血浆皮质类固醇水平。在 HAC15 细胞中,BDE-47 显著增加了基础和刺激的醛固酮和皮质醇分泌。参与皮质类固醇合成和线粒体代谢的几种酶的基因表达也增加了。在 Sprague Dawley 大鼠中,BDE-47 处理组的肾上腺但不是心脏、肾脏或肝脏重量显著增加。100μg BDE-47/kg 处理组的血浆皮质酮水平显著升高。BDE-47 暴露后,血浆醛固酮水平没有变化。这些数据表明 BDE-47 扰乱了皮质类固醇分泌的调节,并进一步证明 PBDEs 是潜在的内分泌干扰物。未来的研究将确定改变皮质类固醇产生的潜在分子机制,并检查这些变化是否会导致我们的 16 周 BDE-47 暴露啮齿动物模型中的潜在心血管疾病。