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首页> 外文期刊>Aquatic Toxicology >The synergistic potential of azole fungicides does not directly correlate to the inhibition of cytochrome P450 activity in aquatic invertebrates
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The synergistic potential of azole fungicides does not directly correlate to the inhibition of cytochrome P450 activity in aquatic invertebrates

机译:唑胺杀菌剂的协同潜力与水生无脊椎动物中细胞色素P450活性的抑制不直接相关

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摘要

The ability of azole fungicides to inhibit cytochrome P450 dependent metabolism is proposed to be the main mechanism for their synergizing effect on pyrethroid insecticide toxicity in aquatic invertebrates. This study investigates the correlation between inhibition strength and synergistic potential of azole fungicides in the crustacean Daphnia magna and the insect larvae Chironomus riparius. Inhibition strength was measured in vivo toward the cytochrome P450 catalysed conversion of 7-ethoxycoumarin to 7-hydroxycoumarin (ECOD). Synergistic potentials were determined as the ratio between predicted and observed toxicity of mixtures based on the model of concentration addition (CA) and independent action (IA). Azoles (n = 9-11) enhanced the toxicity of alpha-cypermethrin in D. magna (Synergy ratios CA: 0.8 - 16; IA: 1.1 - 22) and inhibited cytochrome P450 activity by different degrees (IC50: 0.0023 - 36 mu M for D. magna and 0.08 - 24 mu M for C. riparius). Inhibition strengths were strongly correlated in the two organisms (r: 0.937 p: 0.019 for triazoles and r: 0.903 p: 0.097 for imidazoles). Lipophilicity governed the inhibition strength of triazoles in both species (r & 0.9, p & 0.05). No correlation was observed between inhibition strengths and synergistic potentials. Several reasons for the apparent lack of correlation were discussed.
机译:唑脲菌丝抑制细胞色素p450依赖性代谢的能力是其对水生无脊椎动物中拟除虫菊酯杀虫剂毒性的协同作用的主要机制。本研究研究了甲壳动物Daphnia Magna中唑类杀菌剂的抑制强度和协同潜力的相关性和昆虫幼虫骑士riparius。在体内测量抑制强度,朝向7-乙氧基苏格林至7-羟基苏格林(ECOD)的细胞色素P450催化转化率。基于浓度添加(CA)和独立作用(IA)的模型,确定协同潜力作为混合物的预测和观察毒性之间的比率。唑(n = 9-11)增强了D. Magna中α-硫酰甲酰胺的毒性(协同率Ca:0.8 - 16; IA:1.1-22),并通过不同程度抑制细胞色素P450活性(IC50:0.0023 - 36 mu m对于D. MAGNA和0.08 - 24亩M用于C. RIPARIUS)。在两个生物中抑制强度强烈相关(R:0.937 P:0.019用于三唑和R:0.097用于咪唑的0.097)。亲脂性治理了两种物种(R& 0.9,P& 0.05)中三唑的抑制强度。在抑制强度和协同潜力之间没有观察到相关性。讨论了明显缺乏相关性的几个原因。

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