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Developmental toxicity and stress protein responses in zebrafish embryos after exposure to diclofenac and its solvent, DMSO

机译:暴露于双氯芬酸及其溶剂DMSO后斑马鱼胚胎的发育毒性和应激蛋白反应

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摘要

One of the most frequently detected Pharmaceuticals in environmental water samples is the anti-rheumatic drug, diclofenac. Despite its increasing environmental significance, investigations concerning the effects of this drug on the early developmental stages of aquatic species are lacking up to now. To determine the developmental toxicity and proteotoxicity of this drug on the growing fish embryos, eggs of zebrafish were exposed to six concentrations of diclofenac (0, 1, 20, 100, 500, 1000, and 2000 μgl~(-1)) using DMSO as solvent. Early life stage parameters such as egg and embryo mortality, gastrulation, somite formation, movement and tail detachment, pigmentation, heart beat, and hatching success were noted and described within 48- and 96-h of exposure. After the 96-h exposure, the levels of stress proteins (hsp 70) were determined in both the diclofenac-treated and respective DMSO controls. Results showed no significant inhibition in the normal development until the end of 96 h for all exposure groups. However, there was a delay in the hatching time among embryos exposed to 1000 and 2000 μg 1~(-1). Late-hatched embryos (108 h) did not differ morphologically from normally hatched embryos. The mortality and average heart rate data did not show significant differences for all embryos in both diclofenac-treated and DMSO control groups. No significant malformations were likewise noted among all developing embryos throughout the exposure period. The levels of heat shock proteins in diclofenac-treated and control embryos did not differ significantly. DMSO control embryos, on the other hand, showed a concentration-dependent increase in hsp 70 levels. We suggest possible modulating effect of diclofenac in DMSO-triggered expression of stress proteins and this might have a possible repercussion on the use of DMSO as solvent in any toxicity assay. Since the present data indicate no significant embryotoxicity and proteotoxicity induced by diclofenac and due to the fact that the concentrations of diclofenac used in the present study is up to 2000-fold higher than the concentrations detected in the environment, it is unlikely that this drug would pose a hazard to early-life stages of zebrafish.
机译:抗风湿药双氯芬酸是环境水样中最常检测到的药物之一。尽管其对环境的重要性日益提高,但迄今为止,尚未对该药物对水生物种早期发育的影响进行研究。为了确定该药物对正在生长的鱼胚胎的发育毒性和蛋白毒性,使用DMSO将斑马鱼的卵暴露于六种浓度的双氯芬酸(0、1、20、100、500、1000和2000μgl(-1))中。作为溶剂。在暴露的48小时和96小时内,记录并描述了生命早期阶段的参数,例如卵和胚胎的死亡率,胃排卵,瘤形成,运动和尾巴脱离,色素沉着,心跳和孵化成功。暴露96小时后,在双氯芬酸处理的DMSO对照和相应的DMSO对照中均测定了应激蛋白(hsp 70)的水平。结果显示,所有暴露组的正常发育直到96小时结束都没有明显的抑制作用。然而,暴露于1000和2000μg1〜(-1)的胚胎的孵化时间有所延迟。后期孵化的胚胎(108小时)在形态上与正常孵化的胚胎没有区别。在双氯芬酸治疗组和DMSO对照组中,死亡率和平均心率数据均未显示所有胚胎的显着差异。在整个暴露期间,所有发育中的胚胎也未发现明显的畸形。双氯芬酸处理的和对照的胚胎中热休克蛋白的水平没有显着差异。另一方面,DMSO对照胚胎的hsp 70水平呈浓度依赖性增加。我们建议双氯芬酸在DMSO触发的应激蛋白表达中可能具有调节作用,这可能会对在任何毒性测定中使用DMSO作为溶剂产生影响。由于目前的数据表明双氯芬酸没有引起明显的胚胎毒性和蛋白毒性,并且由于本研究中使用的双氯芬酸的浓度比环境中检测到的浓度高出2000倍,因此该药物不太可能会对斑马鱼的生命早期阶段构成危害。

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