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敌百虫中毒后冲动的长期后果:时间进程和个体差异。

Impulsivity as long-term sequelae after chlorpyrifos intoxication: time course and individual differences.

机构信息

Departamento de Neurociencia y Ciencias de la Salud, Universidad de Almería, 04120, La Cañada, Almería, Spain.

出版信息

Neurotox Res. 2011 Jan;19(1):128-37. doi: 10.1007/s12640-009-9149-3. Epub 2010 Jan 20.

Abstract

Chlorpyrifos (CPF) is a common organophosphate (OP) insecticide that has been widely used in agriculture as a pesticide. The primary mechanism of acute toxic action of OPs is initiated by acetylcholinesterase (AChE) inhibition. However, non-AChE targets have also been proposed as alternative that contributes to the acute lethal action and side effects of short or long-term exposure. Recently, we have found that a single dose of 250 mg/kg CPF produces acceleration in acquisition on schedule-induced polydipsia (SIP) procedure 6 months after its administration. Moreover, CPF animals show a higher level of impulsivity in a delay-discounting task 1 year after acute administration, and these effects are potentiated when animals are divided into high (HD) and low (LD) drinkers in SIP. In the present study, rats were injected with a subcutaneous (sc) dose of 250 mg/kg of CPF, and 10 weeks later its effect on delay-discounting task was evaluated. Consequently, these animals were evaluated based on SIP, and divided into two populations (HD and LD) according to their rates of drinking in this task. One year after OP administration, these animals were re-evaluated in a delay-discounting task. Results revealed that the CPF-administered rats prefer immediate reward and show a more impulsive choice, 10 weeks after CPF administration. Furthermore, 1 year after it administration, only animals treated with CPF that are high drinkers on SIP are more impulsive than the rest of the groups Therefore, these data suggest that some individuals are more sensitive to OP intoxication than the others, at least in terms of durability of sequelae.

摘要

毒死蜱(CPF)是一种常见的有机磷(OP)杀虫剂,曾广泛用于农业作为农药。OP 的急性毒性作用的主要机制是由乙酰胆碱酯酶(AChE)抑制引起的。然而,也提出了非 AChE 靶标作为替代物,有助于急性致死作用和短期或长期暴露的副作用。最近,我们发现单次给予 250mg/kg CPF,在给药后 6 个月会加速在日程诱导性多饮(SIP)程序中的获得。此外,CPF 动物在延迟折扣任务中表现出更高的冲动水平,1 年后急性给药时,这些效应会增强,当动物在 SIP 中分为高(HD)和低(LD)饮酒者时,效应会增强。在本研究中,大鼠皮下(sc)注射 250mg/kg 的 CPF,10 周后评估其对延迟折扣任务的影响。因此,这些动物根据 SIP 进行评估,并根据它们在该任务中的饮酒率分为两个群体(HD 和 LD)。OP 给药 1 年后,这些动物在延迟折扣任务中重新评估。结果表明,CPF 给药大鼠在 CPF 给药 10 周后更喜欢即时奖励,并表现出更冲动的选择。此外,给药 1 年后,只有在 SIP 中高饮酒的 CPF 处理动物比其他组更冲动。因此,这些数据表明,一些个体比其他人对 OP 中毒更敏感,至少在后遗症的持久性方面是如此。

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