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藻类中四种 strobilurins 的急性毒性及相关机制。

Acute toxicity and associated mechanisms of four strobilurins in algae.

机构信息

Department of Applied Chemistry, College of Sciences, China Agricultural University, 2 Yuanmingyuan West Road, Haidian District, Beijing 100193, People's Republic of China.

Center for Environmental and Human Toxicology, Department of Environmental and Global Health, College of Public Health and Health Professions, University of Florida, 2187 Mowry Road, Gainesville, FL, 32611, USA.

出版信息

Environ Toxicol Pharmacol. 2018 Jun;60:12-16. doi: 10.1016/j.etap.2018.03.021. Epub 2018 Apr 3.

Abstract

Strobilurins have been reported highly toxic to non-target aquatic organisms but few illustrated how they cause toxic effects on algae. This study investigated the acute toxicity of Kresoxim-methy (KRE), Pyraclostrobin (PYR), Trifloxystrobin (TRI) and Picoxystrobin (PIC) on two algae and their toxicity mechanisms. Four strobilurins showed lower toxic effects on Chlorella pyrenoidsa but higher on Chlorella vulgaris. bc1 complex activities in C. vulgaris were significantly inhibited by all strobilurins, suggesting bc 1 complex might be the target of strobilurin toxicity in algae. Moreover, SOD, CAT and POD activities were significantly up-regulated by all doses of KRE, PYR and PIC. In contrast, low concentrations of TRI stimulated SOD and POD activities but highest concentration significantly inhibited those activities. Comet assays showed damaged DNA in C. vulgaris by four strobulirins, suggesting their potential genotoxic threats to algae. The results illustrated acute toxicity by strobulirins on algae and their possible toxicity mechanisms.

摘要

啶酰菌胺、吡唑醚菌酯、肟菌酯和唑菌胺酯已被报道对非靶标水生生物具有高毒性,但很少有研究说明它们对藻类产生毒性影响的机制。本研究调查了啶酰菌胺、吡唑醚菌酯、肟菌酯和唑菌胺酯对两种藻类的急性毒性及其毒性机制。四种啶酰菌胺类化合物对蛋白核小球藻的毒性较低,但对普通小球藻的毒性较高。所有啶酰菌胺类化合物均显著抑制普通小球藻的 bc1 复合物活性,表明 bc1 复合物可能是藻类啶酰菌胺类化合物毒性的靶标。此外,所有浓度的 KRE、PYR 和 PIC 均显著上调 SOD、CAT 和 POD 的活性。相比之下,低浓度的 TRI 刺激 SOD 和 POD 的活性,但最高浓度显著抑制这些活性。彗星试验表明,四种啶酰菌胺类化合物对普通小球藻的 DNA 造成损伤,表明它们可能对藻类具有潜在的遗传毒性威胁。这些结果说明了啶酰菌胺类化合物对藻类的急性毒性及其可能的毒性机制。

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