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首页> 外文期刊>Environmental Science and Pollution Research >Short-term exposure to tricyclic antidepressants delays righting time in marine and freshwater snails with evidence for low-dose stimulation of righting speed by imipramine
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Short-term exposure to tricyclic antidepressants delays righting time in marine and freshwater snails with evidence for low-dose stimulation of righting speed by imipramine

机译:短期暴露于三环抗抑郁药的延迟在海洋和淡水蜗牛中的特征时间,具有脂蛋白酶的低剂量刺激的证据

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摘要

Active pharmaceutical ingredients such as tricyclic antidepressants (TCAs) are contaminants of emerging concern which are commonly detected in wastewater effluent and which can disrupt the behavior of non-target organisms. In aquatic snails, the righting response is a critical behavior that has been shown to be inhibited by exposure to SSRI-type antidepressants. We exposed marine and freshwater snails to three tricyclic antidepressants (clomipramine, amitriptyline, and imipramine) for 1h and measured righting response time. In the marine mud snail (Ilyanassa obsoleta), all three TCAs significantly increased righting time at concentrations as low as 156g/L. Similarly, in the freshwater snail Leptoxis carinata, all three TCAs increased righting time at concentrations as low as 263g/L. However, exposure to imipramine from 15.8 to 316g/L resulted in significantly faster righting time. Such low-dose stimulation and high-dose inhibition are characteristics of a hormetic response. We discuss the possible physiological mechanism of action of TCAs and other antidepressants on snail behavior, and the occurrence of non-monotonic, hormetic dose responses to human pharmaceuticals in the aquatic environment.
机译:活性药物成分如三环抗抑郁药(TCAS)是出现令人担忧的污染物,其在废水流出物中通常检测到,这可能破坏非靶毒性生物的行为。在水生蜗牛中,右响应是通过暴露于SSRI型抗抑郁药而被证明的关键行为。我们将海洋和淡水蜗牛暴露于三个三环抗抑郁药(Clomipramine,Amitriptyline和Inipramine),以进行1小时并测量右侧响应时间。在海洋泥蜗牛(Ilyanassa Obsoleta)中,所有三种TCA在浓度下显着增加了低至156g / L的浓度。同样,在淡水蜗牛蛹蛹中,所有三种TCA都会在低至263g /升的浓度下增加统一时间。然而,从15.8至316g / l暴露于脂催化剂导致较快的提取时间更快。这种低剂量刺激和高剂量抑制是刺激反应的特征。我们讨论了TCAS和其他抗抑郁药的可能性机制和其他抗抑郁药对蜗牛行为的发生,以及对水生环境中的人类药物的非单调剂量反应的发生。

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