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Caenorhabditis elegans Neuromuscular Junction: GABA Receptors and Ivermectin Action

机译:秀丽隐杆线虫神经肌肉连接:GABA受体和伊维菌素的作用

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摘要

The prevalence of human and animal helminth infections remains staggeringly high, thus urging the need for concerted efforts towards this area of research. GABA receptors, encoded by the unc-49 gene, mediate body muscle inhibition in Caenorhabditis elegans and parasitic nematodes and are targets of anthelmintic drugs. Thus, the characterization of nematode GABA receptors provides a foundation for rational anti-parasitic drug design. We therefore explored UNC-49 channels from C. elegans muscle cultured cells of the first larval stage at the electrophysiological and behavioral levels. Whole-cell recordings reveal that GABA, muscimol and the anthelmintic piperazine elicit macroscopic currents from UNC-49 receptors that decay in their sustained presence, indicating full desensitization. Single-channel recordings show that all drugs elicit openings of ∼2.5 pA (+100 mV), which appear either as brief isolated events or in short bursts. The comparison of the lowest concentration required for detectable channel opening, the frequency of openings and the amplitude of macroscopic currents suggest that piperazine is the least efficacious of the three drugs. Macroscopic and single-channel GABA-activated currents are profoundly and apparently irreversibly inhibited by ivermectin. To gain further insight into ivermectin action at C. elegans muscle, we analyzed its effect on single-channel activity of the levamisol-sensitive nicotinic receptor (L-AChR), the excitatory receptor involved in neuromuscular transmission. Ivermectin produces a profound inhibition of the frequency of channel opening without significant changes in channel properties. By revealing that ivermectin inhibits C. elegans muscle GABA and L-AChR receptors, our study adds two receptors to the already known ivermectin targets, thus contributing to the elucidation of its pleiotropic effects. Behavioral assays in worms show that ivermectin potentiates piperazine-induced paralysis, thus suggesting that their combination is a good strategy to overcome the increasing resistance of parasites, an issue of global concern for human and animal health.
机译:人类和动物蠕虫感染的发生率仍然高得惊人,因此,迫切需要在这一研究领域作出共同努力。由unc-49基因编码的GABA受体介导秀丽隐杆线虫和寄生线虫体内的肌肉抑制,并且是驱虫药的目标。因此,线虫GABA受体的表征为合理的抗寄生虫药物设计提供了基础。因此,我们在电生理和行为水平上从幼虫第一阶段的秀丽隐杆线虫肌肉培养细胞中探索了UNC-49通道。全细胞记录显示,GABA,麝香酚和驱虫性哌嗪从UNC-49受体引起宏观电流,这些电流在持续存在时衰减,表明完全脱敏。单通道记录表明,所有药物都会引起〜2.5 pA(+100 mV)的开孔,这些开孔要么表现为短暂的孤立事件,要么短暂爆发。比较可检测通道开放所需的最低浓度,开放频率和宏观电流幅度表明,哌嗪在三种药物中效果最低。伊维菌素对宏观和单通道GABA激活的电流具有不可逆的抑制作用。为了进一步了解伊维菌素在秀丽隐杆线虫肌肉上的作用,我们分析了其对乙酰氨基酚敏感性烟碱样受体(L-AChR)(参与神经肌肉传递的兴奋性受体)的单通道活性的影响。伊维菌素对通道开放的频率产生了深远的抑制作用,而通道特性没有明显变化。通过揭示伊维菌素抑制线虫肌肉的GABA和L-AChR受体,我们的研究在已知的伊维菌素靶标上增加了两种受体,从而有助于阐明其多效性作用。蠕虫中的行为分析表明,伊维菌素增强了哌嗪诱导的麻痹,因此表明它们的组合是克服寄生虫抵抗力不断提高的好策略,寄生虫是人类和动物健康普遍关注的问题。

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  • 总页数 9
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