Gilbert M E, Acheson S K, Mack C M, Crofton K M
NSI Technology Services Corporation, Environmental Sciences, Research Triangle Park, North Carolina 27709.
Neurotoxicology. 1990 Spring;11(1):73-86.
Pyrethroid insecticides have recently been purported to possess strong proconvulsant potential. The seizure-inducing properties of two pyrethroids were assessed by pentylenetetrazol (PTZ) seizure models (repeated ip, suprathreshold ip, and iv), and electrical kindling of the amygdala. The efficacy of po versus ip routes of deltamethrin administration was compared using iv-PTZ administration and tests of locomotor activity in a figure-eight maze. Both po and ip deltamethrin produced comparable decreases in motor activity indicating the effectiveness of both of these exposure routes on biological activity. The Type I pyrethroid, cismethrin (15 mg/kg, po), produced a 17% reduction in the threshold dosage of ip-PTZ required to induce a seizure, while delaying the onset of generalized seizure activity. The Type II pyrethroid, deltamethrin (10 mg/kg, po), failed to alter threshold or latency to seizure onset, but did increase seizure duration. No differences were revealed between po (0, 10, 15 mg/kg) or ip (0, 1, 10 mg/kg) administered deltamethrin on seizure thresholds or durations following iv-PTZ. Seizure severity, however, was enhanced by pyrethroids administered po in the iv-PTZ and suprathreshold-ip PTZ tests, ip deltamethrin was without effect. Cismethrin (0, 8, 15 mg/kg) and deltamethrin (0, 6, 10 mg/kg) administered po daily, 2 hours prior to electrical kindling stimulation facilitated amygdala kindling to a minimal but equivalent degree at the highest dosage. This dosage also evoked strong behavioral signs of toxicity. Deltamethrin also induced spontaneous seizures in partially kindled animals in the absence of stimulation. Thus strong evidence of proconvulsant activity of pyrethroids was not evident. The primary effects were limited to an enhancement of seizure severity in response to PTZ (tonic seizures) and the provocation of spontaneous seizures in partially kindled animals.
拟除虫菊酯类杀虫剂最近被认为具有很强的惊厥诱发潜力。通过戊四氮(PTZ)惊厥模型(重复腹腔注射、阈上腹腔注射和静脉注射)以及杏仁核电点燃实验评估了两种拟除虫菊酯的惊厥诱导特性。使用静脉注射PTZ以及在八字形迷宫中进行运动活性测试,比较了溴氰菊酯口服与腹腔注射给药途径的效果。口服和腹腔注射溴氰菊酯均使运动活性出现类似程度的降低,表明这两种给药途径对生物活性均有效。I型拟除虫菊酯顺式氯氰菊酯(15毫克/千克,口服)使诱导惊厥所需的腹腔注射PTZ阈剂量降低了17%,同时延迟了全身性惊厥活动的发作。II型拟除虫菊酯溴氰菊酯(10毫克/千克,口服)未能改变惊厥发作的阈值或潜伏期,但确实增加了惊厥持续时间。静脉注射PTZ后,口服(0、10、15毫克/千克)或腹腔注射(0、1、10毫克/千克)溴氰菊酯对惊厥阈值或持续时间没有差异。然而,在静脉注射PTZ和阈上腹腔注射PTZ实验中,口服拟除虫菊酯会增强惊厥严重程度,腹腔注射溴氰菊酯则无此作用。每天在电点燃刺激前2小时口服顺式氯氰菊酯(0、8、15毫克/千克)和溴氰菊酯(0、6、10毫克/千克),在最高剂量时以最小但相当的程度促进了杏仁核点燃。该剂量还引发了强烈的毒性行为迹象。溴氰菊酯在无刺激情况下也会在部分点燃的动物中诱发自发性惊厥。因此,拟除虫菊酯惊厥诱发活性的有力证据并不明显。主要影响仅限于对PTZ(强直性惊厥)反应时惊厥严重程度的增强以及在部分点燃的动物中引发自发性惊厥。