Gammon D W
Fundam Appl Toxicol. 1985 Feb;5(1):9-23. doi: 10.1016/0272-0590(85)90047-8.
Classical neuropharmacological procedures have been used to elucidate insecticide mode of action in vitro. A good deal has thus been learned about pyrethroids but novel techniques have been necessary to explain the toxicology and symptomology. The free-walking, electrode-implanted cockroach technique, which was developed for this purpose, is described. It enabled correlations to be made between symptomology and effects on specific nerves. The negative temperature coefficient of toxicity of allethrin (the first pyrethroid) was explained in terms of repetitive firing in peripheral (sensory) nerves rather than by nerve blockage, which had been suggested from previous in vitro studies. The elucidation of target sites in vivo and the most useful parameter to study, i.e., repetitive firing in nerve axons, enabled the definition of a pyrethroid resistance mechanism in a major insect pest. It also showed two modes of action for permethrin and cypermethrin, its alpha-cyano analog. A structure-activity relationship for a range of pyrethroids, combining in vitro and in vivo approaches, confirmed two distinct types of pyrethroid action. Studies of poisoning signs and nerve disruptions in vivo in the mouse and cockroach, using diazepam in conjunction with pyrethroids, implicated the GABA-receptor complex as a target for alpha-CN-phenoxybenzyl pyrethroids. This was confirmed by making conductance measurements in crayfish claw opener muscle fibers in vitro.
经典神经药理学方法已被用于在体外阐明杀虫剂的作用方式。因此,人们对拟除虫菊酯有了很多了解,但需要新技术来解释其毒理学和症状学。本文描述了为此目的开发的自由行走、植入电极的蟑螂技术。它能够将症状学与对特定神经的影响联系起来。除虫菊酯(第一种拟除虫菊酯)的负温度系数毒性是根据外周(感觉)神经的重复放电来解释的,而不是根据先前体外研究提出的神经阻滞来解释。对体内靶位点的阐明以及最有用的研究参数,即神经轴突的重复放电,使得能够定义一种主要害虫对拟除虫菊酯的抗性机制。它还显示了氯菊酯及其α-氰基类似物氯氰菊酯的两种作用方式。结合体外和体内方法对一系列拟除虫菊酯的构效关系研究证实了两种不同类型的拟除虫菊酯作用。在小鼠和蟑螂体内使用地西泮与拟除虫菊酯联合研究中毒症状和神经破坏,表明γ-氨基丁酸受体复合物是α-氰基苯氧基苄基拟除虫菊酯的靶标。这在体外对小龙虾爪 opener 肌纤维进行电导测量时得到了证实。