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首页> 外文期刊>Environmental Science and Pollution Research >Acute exposure to the fungicide penconazole affects some biochemical parameters in the crayfish (Astacus leptodactylusEschscholtz, 1823)
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Acute exposure to the fungicide penconazole affects some biochemical parameters in the crayfish (Astacus leptodactylusEschscholtz, 1823)

机译:氨基杀毒剂的急性暴露会影响小龙虾中的一些生化参数(Astacus Leptodactyluseschscholtz,1823)

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摘要

Penconazole is one of the most widely used fungicides all over the world, and since it spreads to large environments, its toxic effects on non-target organisms are of great concern. The toxic effects of penconazole on crayfish (Astacus leptodactylus), which is a bioindicator in freshwater ecosystems and consumed economically, are not known. Therefore, in this study, the purpose was to contribute to the literature on the potential harmful effects of penconazole on a non-target species,Astacus leptodactylus. For this aim, the acute toxicity (96 h) of penconazole was examined. The 96-h LC(50)value of penconazole was detected as 18.7 mg L-1. Four concentrations of penconazole (18.7 mg L-1, 9.35 mg L-1, 4.68 mg L-1, 2.34 mg L-1) were applied to crayfish for 96 h. The results showed that penconazole had destructive effects on esterase mechanisms by inhibiting acetylcholinesterase (AChE) and carboxylesterase (CaE) activities. Significant increases were observed in all antioxidant parameters (superoxide dismutase (SOD), glutathione peroxidase (GPx), glutathione reductase (GR), glutathione S-transferase (GST), reduced glutathione (GSH), malondialdehyde (MDA)) in all doses except the lowest concentration (2.34 mg L-1). All adenosine triphosphatase (ATPase) activities (Na+/K+-ATPase, Mg2+-ATPase, Ca2+-ATPase, total ATPase) had significant dose-related inhibition in both gill and muscle tissues. In summary, our findings show that acute penconazole administration to crayfish causes significant toxic effects on esterase, antioxidative parameters, and metabolic enzymes.
机译:戊菌唑为世界各地使用最广泛的杀菌剂之一,因为它蔓延到大型环境中,其对非靶标生物毒性作用受到极大关注。戊菌唑的上小龙虾的毒性作用(螯leptodactylus),这是在淡水生态系统一个指示生物和经济消耗,是未知的。因此,在这项研究中,目的是促进文学上对非靶标生物,螯leptodactylus戊菌唑的潜在有害影响。对于这个目的,戊菌唑的急性毒性(96小时)进行了研究。 96小时LC检测戊菌唑(50)的值作为18.7毫克L-1。四个浓度戊菌唑的(18.7毫克L-1,9.35毫克L-1,4.68毫克L-1,2.34毫克L-1)被施加到小龙虾96小时。结果表明,戊菌唑有通过抑制乙酰胆碱酯酶和羧酸酯酶(CAE)活动酯酶机制的破坏作用。在所有的抗氧化剂参数中观察到显著增加(超氧化物歧化酶(SOD),谷胱甘肽过氧化物酶(GPx的),谷胱甘肽还原酶(GR),谷胱甘肽S-转移酶(GST),还原型谷胱甘肽(GSH),丙二醛(MDA))在所有剂量除的最低浓度(2.34毫克L-1)。所有三磷酸腺苷酶(ATP酶)活性(钠+ / K + -ATP酶,镁+ -ATP酶,钙+ -ATP酶,ATP酶总)具有在两个鳃和肌肉组织显著剂量相关的抑制作用。总之,我们的研究结果表明,急性戊菌唑政府对小龙虾导致酯酶,抗氧化参数和代谢酶显著的毒性作用。

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