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六溴环十二烷诱导海洋泥鳅(Oryzias melastigma)胚胎发育毒性的机制。

Mechanisms of hexabromocyclododecanes induced developmental toxicity in marine medaka (Oryzias melastigma) embryos.

机构信息

State Key Laboratory of Marine Environmental Science and Key Laboratory of the Ministry of Education for Coastal and Wetland Ecosystems, Xiamen University, Xiamen 361102, China.

State Key Laboratory of Marine Environmental Science and Key Laboratory of the Ministry of Education for Coastal and Wetland Ecosystems, Xiamen University, Xiamen 361102, China.

出版信息

Aquat Toxicol. 2014 Jul;152:173-85. doi: 10.1016/j.aquatox.2014.04.010. Epub 2014 Apr 18.

Abstract

Hexabromocyclododecanes (HBCDs) are widely used as additive brominated flame retardants, and are now ubiquitous contaminants in the environmental media and biota, including the marine environment and marine organisms. However, the impacts of HBCDs on marine fish are not well known. In this study the embryos of marine medaka (Oryzias melastigma) were used to assess the developmental toxicity of HBCDs. Freshly fertilized marine medaka embryos were exposed to various concentrations of technical HBCD (tHBCD, 0, 5, 20 and 50μg/L) until the first fry stage, and hatch success, morphology and cardiac function were examined. In all the exposure groups (5, 20 and 50μg/L) tHBCD significantly increased the embryo heart beats. The measurement of sinus venosus-bulbus arteriosus (SV-BA) distance indicated that tHBCD significantly enlarged the SV-BA distance at exposure concentrations of 20 and 50μg/L. The malformation rate at the first fry stage was also induced by tHBCD in a dose dependent manner, with the formation of pericardial edema and yolk sac edema as the most frequently observed malformation. In addition, the concentrations of total HBCD isomers (ΣHBCDs) in embryos in the current study were comparative with environmental levels and increased with increasing exposure duration. Furthermore, exposure to tHBCD also induced the level of 8-oxodG, a representative oxidative DNA damage. The mechanisms of HBCD-induced developmental toxicity were further explored by TUNEL assay, gel-based quantitative proteomic approach and measurement of the expression of several stress responsive genes, such as p53, TNF-α, IL-1β, CYP1A, COX-1 and COX-2, together with the activities of caspases. The results suggested that HBCDs exposure at environmentally realistic concentrations induced oxidative stress and apoptosis, and suppressed nucleotide and protein synthesis, which all together resulted in developmental toxicity, particularly in the cardiovascular system, in the embryos of O. melastigma.

摘要

六溴环十二烷(HBCDs)被广泛用作添加型溴系阻燃剂,现已成为环境介质和生物群,包括海洋环境和海洋生物体内无处不在的污染物。然而,HBCDs 对海洋鱼类的影响尚不清楚。在这项研究中,利用海洋青鳉(Oryzias melastigma)的胚胎来评估 HBCDs 的发育毒性。将新鲜受精的海洋青鳉胚胎暴露于不同浓度的技术六溴环十二烷(tHBCD,0、5、20 和 50μg/L),直到第一孵育阶段,然后检查孵化成功率、形态和心脏功能。在所有暴露组(5、20 和 50μg/L)中,tHBCD 显著增加了胚胎的心跳。窦房结-动脉干(SV-BA)距离的测量表明,tHBCD 显著增大了 20 和 50μg/L 暴露浓度下的 SV-BA 距离。tHBCD 还以剂量依赖的方式诱导第一孵育阶段的畸形率,以心包水肿和卵黄囊水肿的形成最为常见。此外,本研究中胚胎中总 HBCD 异构体(ΣHBCDs)的浓度与环境水平相当,并随暴露持续时间的增加而增加。此外,暴露于 tHBCD 还诱导了 8-氧代鸟嘌呤(8-oxodG)的水平,8-oxodG 是一种代表性的氧化 DNA 损伤。通过 TUNEL 测定、凝胶定量蛋白质组学方法和几种应激反应基因(如 p53、TNF-α、IL-1β、CYP1A、COX-1 和 COX-2)的表达以及半胱天冬酶活性的测量,进一步探讨了 HBCD 诱导的发育毒性机制。结果表明,在环境现实浓度下暴露于 HBCDs 会引起氧化应激和细胞凋亡,并抑制核苷酸和蛋白质合成,这一切共同导致了 O. melastigma 胚胎的发育毒性,特别是在心血管系统中。

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