Laboratoire Signalisation Fonctionnelle des Canaux Ioniques et des Récepteurs (SiFCIR), UPRES EA 2647, USC INRA 1330, SFR QUASAV 4207, UFR Sciences, Université d'Angers, 2 boulevard Lavoisier, 49045, Angers, cedex, France.
Institute of Physics, Faculty of Physics, Astronomy and Informatics, N. Copernicus University, Torun, Poland.
Sci Rep. 2020 Apr 22;10(1):6842. doi: 10.1038/s41598-020-63957-x.
The insect repellent IR3535 is one of the important alternative in the fight against mosquito-borne disease such as malaria, dengue, chikungunya, yellow fever and Zika. Using a multidisciplinary approach, we propose the development of an innovative insecticide-based vector control strategy using an unexplored property of IR3535. We have demonstrated that in insect neurosecretory cells, very low concentration of IR3535 induces intracellular calcium rise through cellular mechanisms involving orthosteric/allosteric sites of the M1-muscarinic receptor subtype, G protein βγ subunits, background potassium channel inhibition generating depolarization, which induces voltage-gated calcium channel activation. The resulting internal calcium concentration elevation increases nicotinic receptor sensitivity to the neonicotinoid insecticide thiacloprid. The synergistic interaction between IR3535 and thiacloprid contributes to significantly increase the efficacy of the treatment while reducing concentrations. In this context, IR3535, used as a synergistic agent, seems to promise a new approach in the optimization of the integrated vector management for vector control.
驱蚊剂 IR3535 是对抗疟疾、登革热、基孔肯雅热、黄热病和寨卡病毒等蚊媒疾病的重要替代物之一。我们采用多学科方法,提出了利用 IR3535 的未开发特性开发创新的基于杀虫剂的病媒控制策略。我们已经证明,在昆虫神经分泌细胞中,非常低浓度的 IR3535 通过涉及 M1 毒蕈碱受体亚型、G 蛋白 βγ 亚基、背景钾通道抑制产生去极化的正位/变构位点的细胞机制诱导细胞内钙升高,从而诱导电压门控钙通道激活。由此产生的内部钙浓度升高增加了烟碱型乙酰胆碱受体对新烟碱类杀虫剂噻虫啉的敏感性。IR3535 和噻虫啉之间的协同相互作用有助于显著提高治疗效果,同时降低浓度。在这种情况下,作为协同剂的 IR3535 似乎有望为优化综合病媒管理以进行病媒控制提供一种新方法。