Cardona D, López-Grancha M, López-Crespo G, Nieto-Escamez F, Sánchez-Santed F, Flores P
Departamento de Neurociencia y Ciencias de la Salud, Universidad de Almería, La Cañada, Almería, 04120, Spain.
Psychopharmacology (Berl). 2006 Nov;189(1):47-57. doi: 10.1007/s00213-006-0547-4. Epub 2006 Oct 3.
Chlorpyrifos (CPF) is a common organophosphate (OP) insecticide that has been widely used in extensive agriculture as a pesticide. The primary mechanism of acute toxic action of OPs is inhibition of acetylcholinesterase (AChE). However, targets other than AChE have been proposed to contribute to the acute lethal action and side effects of short- or long-term exposure to these compounds. Bekkedal et al. (Sci Total Environ 274:119-123;2001) showed that chronic administration of the OP trimethylolpropane phosphate (TMPP) reduces the number of schedule-induced polydipsia (SIP) sessions necessary to induce asymptotic drinking level.
In the present work, rats were injected with 250 mg/kg CPF and 6 months later, its effect on schedule-induced polydipsia was evaluated. In addition, after stable levels of SIP, a pharmacological study was carried out to determine the implication of other systems in the long-term effects of OPs. Finally, these animals were evaluated in a delay discounting task, as a measure of impulsivity.
Results indicate that the CPF group gives more licks to obtain the same amount of water than control rats (VHC). Moreover, the administration of diazepam produces an increased water intake in the CPF without any observable effect in VHC rats. Data of the delay discounting task show that CPF rats prefer an immediate reward and show a major impulsive choice.
Taken together, our data confirm and extend the long-term behavioral effects of subcutaneous administration of CPF and point to a role for other systems that, besides AChE inhibition, contribute to the long-term neurotoxicity of CPF.
毒死蜱(CPF)是一种常见的有机磷酸酯(OP)杀虫剂,已作为农药广泛应用于粗放型农业。OP急性毒性作用的主要机制是抑制乙酰胆碱酯酶(AChE)。然而,有人提出除AChE外的其他靶点也会导致短期或长期接触这些化合物所产生的急性致死作用和副作用。贝凯达尔等人(《科学的总环境》274:119 - 123;2001年)表明,长期给予OP三羟甲基丙烷磷酸酯(TMPP)可减少诱导渐近饮水水平所需的定时诱导多饮(SIP)次数。
在本研究中,给大鼠注射250mg/kg的CPF,6个月后评估其对定时诱导多饮的影响。此外,在SIP水平稳定后,进行了一项药理学研究,以确定其他系统在OP长期效应中的作用。最后,对这些动物进行延迟折扣任务评估,作为冲动性的一种衡量指标。
结果表明,与对照大鼠(VHC)相比,CPF组为获取等量水舔舐的次数更多。此外,给予地西泮会使CPF组的饮水量增加,而对VHC大鼠没有任何明显影响。延迟折扣任务的数据表明,CPF大鼠更喜欢即时奖励,且表现出更明显的冲动选择。
综上所述,我们的数据证实并扩展了皮下注射CPF的长期行为效应,并指出除抑制AChE外,其他系统在CPF长期神经毒性中也发挥作用。