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Chloride Channels as Tools for Developing Selective Insecticides

机译:氯离子通道作为开发选择性杀虫剂的工具

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ligand-gated chloride channels underlie inhibition in excitable membranes and are proven target sites for insecticides.The gamma-aminobutyric acid (GABA~1) receptor/chloride ionophore complex is the primary sitge of action for a number of currently used insecticides,such as lindane,endosulfan,and fipronil.These compounds act as antaqonists by stabilizing nonconducting conformations of the chloride channel.Blockate of the GABA-gated chloride channel reduces neuronal inhibition,which leads to hyperexcitation of the central nervous system,convulsions,and death.We recently investigated the mode of action of the siliphinenes,plant-derived natural compounds that structurally resemble picrotoxinin.These materials antagonize the action of GABA on insect neurons and block GABA-mediated chloride uptake into mouse brain synatponeurosomes in a noncompetitive manner.In mammals,avermectins have a blocking action on the GABA-gated chloride channel consistent with a coarse tremor,whereas at longer times and higher concentrations,activation of the channel suppresses neuronal activity.Inverte-brates display ataxia,paralysis,and death as the predominant signs of poisoning,with a glutamate-gated chloride channel playing a major role.Additional target site4s for the avermectins or other chloride channel-directed compounds might include recaptors gated by histamine,serotonin,or acetylcholine.The voltage-senisitive chloride channels form another large gene family of chloride channels.Voltage-dependent chloride channels are involved in anumber of physiological processes including:maintenance of electrical excitability,chloride ion secretion and resorption,intravesicular acidification,and cell volume regulation.A subset of these channels is affected by convulsants andinsecticides in mammals,although th role they play in acute lethality in insects is unclear.Given the wide range of functions that they mediate,these channels are also potential targets for insecticide development.
机译:配体门控的氯离子通道是可兴奋膜上的抑制因子,是公认的杀虫剂目标部位。γ-氨基丁酸(GABA〜1)受体/氯化物离子载体复合物是许多目前使用的杀虫剂(如林丹)的主要作用部位,硫丹和氟虫腈。这些化合物通过稳定氯化物通道的非传导性构象而充当拮抗剂。GABA门控氯化物通道的阻塞会减少神经元抑制作用,从而导致中枢神经系统过度兴奋,抽搐和死亡。硅磷脂的作用方式,是植物衍生的天然化合物,在结构上类似于苦瓜毒素。这些物质拮抗GABA对昆虫神经元的作用,并以非竞争性方式阻止GABA介导的氯摄取到小鼠脑突触神经小体中。在哺乳动物中,阿维菌素具有一种在GABA门控氯化物通道上的阻断作用与粗大震颤相一致,而在更长的时间es和更高的浓度,通道的激活抑制神经元活动。无脊椎动物显示共济失调,瘫痪和死亡是中毒的主要迹象,谷氨酸盐酸盐的氯离子通道起主要作用。阿维菌素或其他药物的其他靶位点4s。氯离子通道导向的化合物可能包括被组胺,5-羟色胺或乙酰胆碱门控的捕获子。电压敏感的氯离子通道形成了另一个大的氯离子基因家族。电压依赖性氯离子通道涉及许多生理过程,包括:维持电兴奋性,氯离子的分泌和吸收,囊泡内酸化和细胞体积调节。这些通道中的一部分受惊厥和杀虫剂影响,尽管它们在昆虫的急性致死性中所起的作用尚不清楚。鉴于它们介导的多种功能这些渠道也是杀虫剂开发的潜在目标。

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