Fiocruz, Centro de Estudos em Saúde do Trabalhador e Ecologia Humana (CESTEH), Escola Nacional de Saúde Pública (ENSP), Av. Brasil, 4.365, Manguinhos, 21040-360 Rio de Janeiro, RJ, Brazil.
PUC-Rio, Departamento de Química, Gávea, 22453-900 Rio de Janeiro, RJ, Brazil.
Ecotoxicol Environ Saf. 2019 Apr 30;171:781-789. doi: 10.1016/j.ecoenv.2019.01.041. Epub 2019 Jan 17.
Contaminants of emerging concern have become an important environmental problem, especially pharmaceutically active compounds (PhACs), since, after use, these drugs return to the environment, contaminating aquatic ecosystems. Some may display the ability to bioaccumulate and biomagnify throughout the food chain, leading to potential environmental and human deleterious effects which are, however, still largely unknown. In this context, the aim of the present study was to evaluate the effect of two psychotropic drugs commonly found in the environment, carbamazepine (CBZ) and clonazepam (CZP), both isolated and co-administrated, on oxidative stress biomarkers and essential metal homeostasis in Danio rerio fish specimens. No studies are available to data in this regard concerning CZP effects on fish. Reduced Glutathione (GSH), Metallothionein (MT), Catalase (CAT) and Glutathione S-Transferase (GST) were determined, as well as essential metals in fish liver, kidney and brains. Significant oxidative stress effects were observed for several biomarkers, where brain GST activity was the most affected, mainly with regard to CBZ exposure, while GST and CAT activity in the liver were downregulated in the co-administration mixture. In addition, dishomeostasis of several essential elements was detected in all analyzed organs, with a synergistic action of CBZ and CZP in brain, decreasing basal Mg, Al, K, Fe, Co, Ni and Cu levels in this organ, the target site for these drugs in humans. The brain organ was the most affected as observed by altered GST activity and metal dyshomeostasis concerning exposure to both compounds. These compounds, thus, present health risks to the aquatic biota, due to the evidenced deleterious effects and their constant release into the environment due to widespread use. Steps are needed to implement adequate legislation for risk analysis and decision-making in order to mitigate the effects of these emerging contaminants on aquatic ecosystem health.
新兴关注污染物已成为一个重要的环境问题,尤其是药用活性化合物(PhACs),因为这些药物在使用后会返回环境,污染水生生态系统。一些药物可能具有在食物链中生物积累和生物放大的能力,从而导致潜在的环境和人类有害影响,但这些影响在很大程度上仍未被了解。在这种情况下,本研究的目的是评估两种常见于环境中的精神药物,卡马西平(CBZ)和氯硝西泮(CZP),单独和共同给药,对斑马鱼生物标本氧化应激生物标志物和必需金属内稳态的影响。目前尚无关于 CZP 对鱼类影响的研究。测定了还原型谷胱甘肽(GSH)、金属硫蛋白(MT)、过氧化氢酶(CAT)和谷胱甘肽 S-转移酶(GST)以及鱼类肝脏、肾脏和大脑中的必需金属。几种生物标志物的氧化应激作用明显,其中脑 GST 活性受影响最大,主要与 CBZ 暴露有关,而肝脏 GST 和 CAT 活性在混合物共同给药时下调。此外,所有分析器官中都检测到几种必需元素的失衡,CBZ 和 CZP 在大脑中的协同作用,降低了该器官中 Mg、Al、K、Fe、Co、Ni 和 Cu 的基础水平,这些药物在人类中的靶器官。如 GST 活性改变和金属失衡所示,大脑器官受到的影响最大,涉及到两种化合物的暴露。由于这些化合物具有已证实的有害影响,并且由于广泛使用而不断释放到环境中,因此它们对水生生物群具有健康风险。需要采取措施实施适当的立法,进行风险分析和决策,以减轻这些新兴污染物对水生生态系统健康的影响。