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长期暴露于双酚 S 会损害斑马鱼下丘脑-垂体-肾上腺轴的应激功能,并导致对新奇事物的类似焦虑的行为反应。

Long-term exposure of zebrafish to bisphenol S impairs stress function of hypothalamic-pituitary-interrenal axis and causes anxiety-like behavioral responses to novelty.

机构信息

College of Marine Life Sciences, Ocean University of China, 5 Yushan Road, Qingdao 266003, Shandong province, China.

School of Environmental and Municipal Engineering, Qingdao University of Technology, 11 Fushun Road, Qingdao 266033, Shandong province, China.

出版信息

Sci Total Environ. 2020 May 10;716:137092. doi: 10.1016/j.scitotenv.2020.137092. Epub 2020 Feb 3.

Abstract

Bisphenol S (BPS), a main substitute of bisphenol A, has been reported to induce multiple endocrine disrupting effects on animals, however, whether it can interfere with the corticosteroid-endocrine system still remains unknown. Furthermore, previous studies mainly investigated the influences of environmental pollutants on corticosteroid levels and gene expressions of hypothalamic-pituitary-interrenal/adrenal (HPI/A) axis, while the downstream toxic effects caused thereafter have not yet been fully elucidated. Considering the key role of cortisol, a primary corticosteroid hormone in teleost, in mediating stress adaptation and the highly positive correlation between cortisol level and anxious phenotype in the novel environment, we hypothesized that an imbalanced cortisol homeostasis due to environmental pollutant exposure may further affect the behavioral responses to novelty stress. In the present study, zebrafish, a valuable model in studying human stress physiology and anxiety behavior, were exposed to BPS from embryos to adults (120 days) at environmentally relevant concentrations (1 and 10 μg/L) and 100 μg/L. Results found that long-term exposure to BPS increased whole-body cortisol levels and caused abnormal expressions of HPI axis genes. Moreover, the excessive cortisol levels may be due to the inhibition of cortisol catabolism and excretion, as evidenced by the down-regulated expressions of hydroxysteroid 11-beta dehydrogenase 2 and hydroxysteroid 20-beta dehydrogenase 2 genes. More importantly, as we speculated, excessive cortisol levels may be responsible for the occurrence of anxiety-like behavioral responses indicated by longer latency, fewer time spent in the upper half, and more erratic movements in a 6-min novel tank test. Overall, our study provides basic data for the comprehensive understanding of BPS toxicity, and emphasizes environmental health risks of BPS in inducing anxiety syndrome at environmentally realistic concentrations.

摘要

双酚 S(BPS)作为双酚 A 的主要替代品,已被报道对动物具有多种内分泌干扰作用,然而,它是否会干扰皮质甾类内分泌系统仍不清楚。此外,先前的研究主要调查了环境污染物对皮质甾类水平和下丘脑-垂体-肾上腺(HPI/A)轴基因表达的影响,而此后的下游毒性作用尚未完全阐明。考虑到皮质醇作为鱼类主要皮质甾类激素在介导应激适应中的关键作用,以及在新环境中皮质醇水平与焦虑表型之间的高度正相关,我们假设由于暴露于环境污染物而导致的皮质醇平衡失调可能会进一步影响对新奇应激的行为反应。在本研究中,斑马鱼作为研究人类应激生理学和焦虑行为的一种有价值的模型,从胚胎到成年(120 天)暴露于环境相关浓度(1 和 10 μg/L)和 100 μg/L 的 BPS 中。结果发现,长期暴露于 BPS 会增加全身皮质醇水平并导致 HPI 轴基因异常表达。此外,过量的皮质醇水平可能是由于皮质醇分解代谢和排泄的抑制所致,这一点可从羟固醇 11-β脱氢酶 2 和羟固醇 20-β脱氢酶 2 基因的下调表达中得到证明。更重要的是,正如我们所推测的那样,过量的皮质醇水平可能是导致焦虑样行为反应发生的原因,这表现为在 6 分钟新鱼缸测试中潜伏期更长、在上半部分停留的时间更少以及运动更不稳定。总的来说,我们的研究为全面了解 BPS 的毒性提供了基础数据,并强调了在环境现实浓度下 BPS 引起焦虑综合征的环境健康风险。

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