{"title":"毒死蜱对焦虑+迷宫模型的影响","authors":"M. C. Sánchez-Amate, P. Flores, F. Sánchez-Santed","doi":"10.1097/00008877-200107000-00007","DOIUrl":null,"url":null,"abstract":"The purpose of the present study was to determine the effect of two different doses of the organophosphate insecticide O, O′–diethyl‐O ‐3,5,6‐trichloro‐2‐pyridylphosphorothionate [chlorpyrifos (CPF)], a cholinesterase (ChE) inhibitor, in the plus‐maze test of anxiety in the rat, as well as on acetylcholinesterase (AChE) activity in the brain. In a first experiment, the behavioural methodology was validated by showing the anxiolytic and anxiogenic effects of diazepam and pentylenetetrazole (PTZ), respectively. Acute exposure to CPF (166 mg/kg and 250 mg/kg, s.c.) produced significant dose‐dependent inhibition (54% and 71%, respectively) of whole‐brain AChE 48 hours after treatment. Neither dose produced signs of acute cholinergic toxicity at any time following treatment, as was verified by a functional observational battery. Both doses of CPF were injected 48 h before testing in the plus‐maze and were shown to have anxiogenic effects as demonstrated by the significant decrease in the percentage of time spent and percentage of entries into open arms. This report thus shows clear behavioural alteration as an acute effect of an organophosphate in the absence of any classic sign of cholinergic toxicity. Our results are relevant to the understanding of both the pharmacology of anxiety and the behavioural toxicology of cholinesterase inhibitors.","PeriodicalId":8741,"journal":{"name":"Behavioral Pharmacology","volume":"15 1","pages":"285-292"},"PeriodicalIF":0.0000,"publicationDate":"2001-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"61","resultStr":"{\"title\":\"Effects of chlorpyrifos in the plus‐maze model of anxiety\",\"authors\":\"M. C. Sánchez-Amate, P. Flores, F. Sánchez-Santed\",\"doi\":\"10.1097/00008877-200107000-00007\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"The purpose of the present study was to determine the effect of two different doses of the organophosphate insecticide O, O′–diethyl‐O ‐3,5,6‐trichloro‐2‐pyridylphosphorothionate [chlorpyrifos (CPF)], a cholinesterase (ChE) inhibitor, in the plus‐maze test of anxiety in the rat, as well as on acetylcholinesterase (AChE) activity in the brain. In a first experiment, the behavioural methodology was validated by showing the anxiolytic and anxiogenic effects of diazepam and pentylenetetrazole (PTZ), respectively. Acute exposure to CPF (166 mg/kg and 250 mg/kg, s.c.) produced significant dose‐dependent inhibition (54% and 71%, respectively) of whole‐brain AChE 48 hours after treatment. Neither dose produced signs of acute cholinergic toxicity at any time following treatment, as was verified by a functional observational battery. Both doses of CPF were injected 48 h before testing in the plus‐maze and were shown to have anxiogenic effects as demonstrated by the significant decrease in the percentage of time spent and percentage of entries into open arms. This report thus shows clear behavioural alteration as an acute effect of an organophosphate in the absence of any classic sign of cholinergic toxicity. Our results are relevant to the understanding of both the pharmacology of anxiety and the behavioural toxicology of cholinesterase inhibitors.\",\"PeriodicalId\":8741,\"journal\":{\"name\":\"Behavioral Pharmacology\",\"volume\":\"15 1\",\"pages\":\"285-292\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2001-07-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"61\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Behavioral Pharmacology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1097/00008877-200107000-00007\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Behavioral Pharmacology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1097/00008877-200107000-00007","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 61
摘要
本研究的目的是确定两种不同剂量的有机磷杀虫剂O, O ' -二乙基- O‐3,5,6‐三氯‐2‐吡啶基硫代酸盐[毒死蜱(CPF)],一种胆碱酯酶(ChE)抑制剂,在大鼠焦虑的正迷宫测试中,以及对大脑乙酰胆碱酯酶(AChE)活性的影响。在第一个实验中,行为方法分别通过显示安定和戊四唑(PTZ)的抗焦虑和致焦虑作用得到验证。急性暴露于CPF (166 mg/kg和250 mg/kg, s.c)在治疗后48小时对全脑AChE产生显著的剂量依赖性抑制(分别为54%和71%)。两种剂量在治疗后的任何时间都没有产生急性胆碱能毒性的迹象,这是由功能观察电池证实的。两种剂量的CPF均在阳性迷宫试验前48小时注射,结果显示CPF具有焦虑效应,其表现为花费时间百分比和进入张开双臂百分比的显著减少。因此,本报告表明,在没有任何典型胆碱能毒性迹象的情况下,行为改变是有机磷的急性效应。我们的结果与焦虑的药理学和胆碱酯酶抑制剂的行为毒理学的理解有关。
Effects of chlorpyrifos in the plus‐maze model of anxiety
The purpose of the present study was to determine the effect of two different doses of the organophosphate insecticide O, O′–diethyl‐O ‐3,5,6‐trichloro‐2‐pyridylphosphorothionate [chlorpyrifos (CPF)], a cholinesterase (ChE) inhibitor, in the plus‐maze test of anxiety in the rat, as well as on acetylcholinesterase (AChE) activity in the brain. In a first experiment, the behavioural methodology was validated by showing the anxiolytic and anxiogenic effects of diazepam and pentylenetetrazole (PTZ), respectively. Acute exposure to CPF (166 mg/kg and 250 mg/kg, s.c.) produced significant dose‐dependent inhibition (54% and 71%, respectively) of whole‐brain AChE 48 hours after treatment. Neither dose produced signs of acute cholinergic toxicity at any time following treatment, as was verified by a functional observational battery. Both doses of CPF were injected 48 h before testing in the plus‐maze and were shown to have anxiogenic effects as demonstrated by the significant decrease in the percentage of time spent and percentage of entries into open arms. This report thus shows clear behavioural alteration as an acute effect of an organophosphate in the absence of any classic sign of cholinergic toxicity. Our results are relevant to the understanding of both the pharmacology of anxiety and the behavioural toxicology of cholinesterase inhibitors.