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神经活性药物对鱼类的短期影响:生化和行为影响。

Short-term effects of neuroactive pharmaceutical drugs on a fish species: biochemical and behavioural effects.

机构信息

Department of Biology, University of Aveiro, Portugal; Centre for Environmental and Marine Studies (CESAM), Campus of Santiago, University of Aveiro, Portugal.

出版信息

Aquat Toxicol. 2013 Nov 15;144-145:218-29. doi: 10.1016/j.aquatox.2013.10.005. Epub 2013 Oct 12.

Abstract

The presence of pharmaceutical residues in the aquatic environment is receiving great attention since significant levels of contamination have been found, not only in sewage treatment plant effluents, but also in open waters. In our study, the toxicity of three anticonvulsant drugs commonly found in the environment (diazepam, carbamazepine, and phenytoin) was evaluated in Lepomis gibbosus (pumpkinseed sunfish). This study focused on oxidative stress parameters, namely: glutathione reductase (GRed), glutathione S-transferases (GSTs), catalase (CAT), and lipid peroxidation (thiobarbituric acid reactive substances, TBARS) in the hepatic, digestive, and gill tissues of exposed animals. Simultaneously, we assessed the effects of these drugs in terms of behavioural parameters, such as scototaxis and activity. Exposure to diazepam caused an increase in GST activities in the gills and an inhibition of GRed in the digestive tract, relative to control, suggesting an antioxidant response. It also caused fish to spend more time swimming and less time in a refuge area (black compartment of an aquarium). Exposure to carbamazepine caused an increase in GSTs and GRed activity in the digestive tract, which is not always consistent with the literature. A significant positive correlation was found between carbamazepine concentration and time spent in motion and a negative correlation with time spent in black compartment. Exposure to phenytoin was responsible for adaptive responses in the activities of CAT and GSTs (in the liver), but it did not elicit any behavioural alterations. Although all three drugs seemed to induce oxidative stress in some organs, peroxidative damage (measured as TBARS concentrations) was not found at the selected range of concentrations. Our results enlighten the need for more research on the ecological consequences of pharmaceuticals in the aquatic environment, especially drugs that interfere with the CNS and behaviour, because the net outcome of these effects may be difficult to predict.

摘要

水中环境中的药物残留受到了广泛关注,因为不仅在污水处理厂的废水中,而且在开放水域中都发现了大量的药物残留。在我们的研究中,评估了三种常见环境抗惊厥药物(地西泮、卡马西平和苯妥英)对 Lepomis gibbosus(南瓜籽太阳鱼)的毒性。本研究主要关注氧化应激参数,即暴露动物的肝、肠和鳃组织中的谷胱甘肽还原酶(GRed)、谷胱甘肽 S-转移酶(GSTs)、过氧化氢酶(CAT)和脂质过氧化(硫代巴比妥酸反应物质,TBARS)。同时,我们评估了这些药物对行为参数的影响,如避光性和活性。与对照组相比,地西泮暴露导致鳃中 GST 活性增加,肠道中 GRed 抑制,表明存在抗氧化反应。它还导致鱼花更多的时间游泳,更少的时间在避难区(水族馆的黑色隔间)。卡马西平暴露导致肠道中 GSTs 和 GRed 活性增加,但这并不总是与文献一致。发现卡马西平浓度与运动时间呈显著正相关,与黑色隔间时间呈负相关。苯妥英暴露导致 CAT 和 GSTs(肝脏)活性的适应性反应,但没有引起任何行为改变。尽管这三种药物似乎在某些器官中引起了氧化应激,但在所选浓度范围内没有发现过氧化损伤(用 TBARS 浓度测量)。我们的研究结果表明,需要对水中环境中药物的生态后果进行更多的研究,特别是对干扰中枢神经系统和行为的药物,因为这些影响的净结果可能难以预测。

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