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毒理学、作用模式以及对作用于氯离子通道的杀虫剂的靶位点介导抗性。

Toxicology, mode of action and target site-mediated resistance to insecticides acting on chloride channels.

作者信息

Bloomquist J R

机构信息

Department of Entomology, Virginia Polytechnic Institute and State University, Blacksburg 24061.

出版信息

Comp Biochem Physiol C Comp Pharmacol Toxicol. 1993 Oct;106(2):301-14. doi: 10.1016/0742-8413(93)90138-b.

Abstract
  1. The discovery that the avermectins and cyclodienes affected the chloride channels of excitable membranes generated intense research interest among academic and industrial scientists. 2. The results of biochemical and neurophysiological studies indicate that the gamma-aminobutyric acid (GABA)-gated chloride channel is an important, if not the primary site of action for these compounds. 3. The action of insecticides on the functional properties of the GABA receptor differs by structural class. The cyclodienes block the chloride ion channel and the avermectins activate it. 4. Blockage of the GABA-gated chloride channel by cyclodienes reduces neuronal inhibition, which leads to hyper-excitation of the central nervous system, convulsions, and death. For avermectins, activation of the channel suppresses neuronal activity, resulting in ataxia, paralysis and death. Although actions on the GABA-gated chloride channel can explain many of the effects of these compounds, there is evidence supporting the participation of other ligand- and voltage-gated chloride channels in the overall intoxication process. This consideration is especially true for the avermectins. 5. Several structural series of experimental insecticides have been synthesized which possess a blocking action on the GABA-gated chloride channel similar to that of the cyclodienes. 6. Resistance to cyclodienes usually occurs through an altered target site, and extends to all experimental compounds that block chloride channels. However, the resistance does not afford protection against the avermectins. 7. The continued search for new insecticides directed against chloride channels may lead to compounds with less environmental impact and greater selectivity than that of the cyclodienes. Given the pre-selection for resistance by the cyclodienes, new compounds with a similar mode of action must be used judiciously in order to suppress or delay the re-emergence of widespread resistance.
摘要
  1. 阿维菌素和环二烯类化合物能影响可兴奋膜的氯离子通道这一发现,在学术界和工业界的科学家当中引发了浓厚的研究兴趣。2. 生化和神经生理学研究结果表明,γ-氨基丁酸(GABA)门控氯离子通道即便不是这些化合物的主要作用位点,也是一个重要作用位点。3. 不同结构类别的杀虫剂对GABA受体功能特性的作用有所不同。环二烯类化合物会阻断氯离子通道,而阿维菌素则会激活该通道。4. 环二烯类化合物对GABA门控氯离子通道的阻断会降低神经元抑制作用,从而导致中枢神经系统过度兴奋、惊厥和死亡。对于阿维菌素而言,通道的激活会抑制神经元活动,导致共济失调、麻痹和死亡。尽管对GABA门控氯离子通道的作用可以解释这些化合物的许多效应,但有证据支持其他配体门控和电压门控氯离子通道也参与了整个中毒过程。这一点对于阿维菌素尤为如此。5. 已经合成了几个结构系列的实验性杀虫剂,它们对GABA门控氯离子通道具有与环二烯类化合物类似的阻断作用。6. 对环二烯类化合物的抗性通常是通过靶位点改变产生的,并且会扩展到所有阻断氯离子通道的实验性化合物。然而,这种抗性并不能提供对阿维菌素的防护。7. 持续寻找针对氯离子通道的新型杀虫剂,可能会找到比环二烯类化合物对环境影响更小、选择性更高的化合物。鉴于环二烯类化合物会预先选择产生抗性,具有类似作用模式的新化合物必须谨慎使用,以抑制或延缓广泛抗性的再度出现。

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