Department of Pharmacology & Therapeutics, McGill University, Montreal, QC, H3G 1Y6, Canada.
Department of Obstetrics & Gynecology, McGill University, Montreal, QC, H3G 1Y6, Canada.
Endocrinology. 2023 Aug 1;164(9). doi: 10.1210/endocr/bqad119.
Adverse effects associated with exposure to brominated flame retardants have led to regulations for their use and their replacement with organophosphate esters (OPEs). However, little is known about the impact of OPEs on the adrenal, a vital endocrine gland. Here, we used a high-content screening approach to elucidate the effects of OPEs on H295R human adrenal cell phenotypic endpoints and function. The effects of 2,2',4,4'-tetrabromodiphenyl ether (BDE-47), a legacy brominated flame retardant, on H295R cell cytotoxicity, oxidative stress, mitochondria, lysosomes, and lipid droplets were compared with those of 6 OPEs. Most OPEs reduced oxidative stress, increased the numbers of mitochondria, decreased lysosomes, and increased lipid droplets. Two potency ranking approaches, the lowest benchmark concentration/administered equivalent dose methods and Toxicological Prioritization Index analyses, revealed that the triaryl-OPEs (isopropylated triphenyl phosphate [IPPP], tris(methylphenyl) phosphate [TMPP], and triphenyl phosphate [TPHP]) and 1 nontriaryl OPE (tris(1,3-dichloro-2-propyl) phosphate [TDCIPP]) were more potent than BDE-47. The steroidogenic activity of adrenal cells in the presence or absence of forskolin, a steroidogenic stimulus, was determined after exposure to triaryl-OPEs. The basal production of cortisol and aldosterone was increased by IPPP but decreased by TPHP or TMPP exposure; the response to forskolin was not affected by these OPEs. All 3 triaryl OPEs altered the expression of rate-limiting enzymes involved in cholesterol and steroid biosynthesis; CYP11B1 and CYP11B2 were the most prominently affected targets. The OPE chemical-specific effects on cortisol and aldosterone production were best explained by alterations in STAR expression. Thus, the adrenal may be an important target for these endocrine-disrupting chemicals.
与溴化阻燃剂暴露相关的不良影响导致了对其使用的规定,并将其用有机磷酸酯(OPEs)取代。然而,人们对 OPEs 对肾上腺这一重要内分泌腺的影响知之甚少。在这里,我们使用高通量筛选方法阐明了 OPEs 对 H295R 人肾上腺细胞表型终点和功能的影响。比较了 2,2',4,4'-四溴二苯醚(BDE-47),一种传统的溴化阻燃剂,对 H295R 细胞细胞毒性、氧化应激、线粒体、溶酶体和脂滴的影响与 6 种 OPEs 的影响。大多数 OPEs 降低了氧化应激,增加了线粒体数量,减少了溶酶体,增加了脂滴。两种效力排名方法,最低基准浓度/给予等效剂量方法和毒性优先指数分析,表明三芳基-OPEs(异丙基化三苯基磷酸酯 [IPPP]、三(甲基苯基)磷酸酯 [TMPP] 和三苯基磷酸酯 [TPHP])和 1 种非三芳基 OPE(三(1,3-二氯-2-丙基)磷酸酯 [TDCIPP])比 BDE-47 更有效。在存在或不存在促肾上腺皮质激素刺激物 forskolin 的情况下,测定暴露于三芳基-OPE 后肾上腺细胞的类固醇生成活性。IPPP 增加了皮质醇和醛固酮的基础产生,但 TPHP 或 TMPP 暴露则降低了基础产生;这些 OPE 对促肾上腺皮质激素的反应没有影响。所有 3 种三芳基 OPE 改变了参与胆固醇和类固醇生物合成的限速酶的表达;CYP11B1 和 CYP11B2 是受影响最明显的靶标。OPE 对皮质醇和醛固酮产生的化学特异性影响可以通过 STAR 表达的改变得到最好的解释。因此,肾上腺可能是这些内分泌干扰化学物质的一个重要靶标。