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脂肪酸及相关钾离子通道阻滞剂:对蚊子的毒性及生理作用

Fatty Acid and Related Potassium Kv2 Channel Blockers: Toxicity and Physiological Actions on Mosquitoes.

作者信息

Démares Fabien, Coquerel Quentin, Richoux Gary, Linthicum Kenneth, Bloomquist Jeffrey

机构信息

Neurotoxicology Laboratory, Department of Entomology and Nematology, Emerging Pathogens Institute, University of Florida, Gainesville, FL 32610, USA.

USDA, ARS, Center for Medical, Agricultural and Veterinary Entomology, Gainesville, FL 32608, USA.

出版信息

Insects. 2018 Nov 1;9(4):155. doi: 10.3390/insects9040155.

Abstract

Potassium channels constitute a very diverse group involved in neural signaling, neuronal activity, membrane potential maintenance, and action potential generation. Here, we tested the mammalian potassium channel blockers TRAM-34 and 5-hydroxydecanoate (5-HDC), as well as certain fatty acids (FA) that might fit in the lumen of the pore and block channel activity by obstructing K⁺ ion passage. Kv channel blockers could be leads for a novel pesticide type. Insecticidal activity was assessed by topical application to adult mosquitoes, paralysis in a headless larval assay, at the cellular level with patch-clamp recordings of engineered HEK cells expressing Kv2.1 channels, as well as central nervous system recordings from larval . With only one hydroxyl group difference, decanoic acid had a consistently greater effect than 5-HDC in blocking Kv channels, paralyzing larvae, and killing mosquitoes. The 11-dansylamino undecanoic acid (DAUDA) blockage of eukaryotic Kv channels is demonstrated for the first time, but it failed to kill adult mosquitoes. We synthesized alkyl esters from DAUDA and decanoic acid in an effort to improve cuticular penetration, but it had little impact upon adult toxicity. TRAM-34 and rolipram did not show activity on Kv channels nor potent insecticidal effect on adult mosquitoes. Furthermore, co-application of test compounds with permethrin did not increase mortality in adults. In conclusion, the compounds tested had modest insecticidal and synergistic activity.

摘要

钾通道是一个非常多样化的群体,参与神经信号传导、神经元活动、膜电位维持和动作电位产生。在这里,我们测试了哺乳动物钾通道阻滞剂TRAM - 34和5 - 羟基癸酸(5 - HDC),以及某些可能适合孔腔并通过阻碍K⁺离子通道来阻断通道活性的脂肪酸(FA)。Kv通道阻滞剂可能成为新型杀虫剂的先导物。通过局部涂抹于成年蚊子、在无头幼虫试验中观察麻痹情况、在细胞水平上对表达Kv2.1通道的工程化HEK细胞进行膜片钳记录以及对幼虫进行中枢神经系统记录来评估杀虫活性。仅相差一个羟基,癸酸在阻断Kv通道、麻痹幼虫和杀死蚊子方面的效果始终比5 - HDC更强。首次证明了11 - 丹磺酰氨基十一烷酸(DAUDA)对真核Kv通道的阻断作用,但它未能杀死成年蚊子。我们从DAUDA和癸酸合成了烷基酯,以提高表皮渗透性,但对成虫毒性影响不大。TRAM - 34和咯利普兰对Kv通道没有活性,对成年蚊子也没有显著的杀虫作用。此外,测试化合物与氯菊酯联合使用并未增加成虫的死亡率。总之,所测试的化合物具有适度的杀虫和协同活性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e782/6315728/9ce1bbd3e8e2/insects-09-00155-g001.jpg

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