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多日治疗后,(+)-甲基苯丙胺和(+/-)-3,4-亚甲基二氧基甲基苯丙胺对新生大鼠单胺和皮质酮水平的短期及长期影响。

Short- and long-term effects of (+)-methamphetamine and (+/-)-3,4-methylenedioxymethamphetamine on monoamine and corticosterone levels in the neonatal rat following multiple days of treatment.

作者信息

Schaefer Tori L, Skelton Matthew R, Herring Nicole R, Gudelsky Gary A, Vorhees Charles V, Williams Michael T

机构信息

Division of Neurology, Department of Pediatrics, Cincinnati Children's Research Foundation and University of Cincinnati College of Medicine, Cincinnati, Ohio, USA.

出版信息

J Neurochem. 2008 Mar;104(6):1674-85. doi: 10.1111/j.1471-4159.2007.05112.x. Epub 2007 Nov 6.

Abstract

Rats treated with (+/-)-3,4-methylenedioxymethamphetamine (MDMA) or (+)-methamphetamine (MA) neonatally exhibit long-lasting learning impairments (i.e., after treatment on postnatal days (P)11-15 or P11-20). Although both drugs are substituted amphetamines, they each produce a unique profile of cognitive deficits (i.e., spatial vs. path integration learning and severity of deficits) which may be the result of differential early neurochemical changes. We previously showed that MA and MDMA increase corticosterone (CORT) and MDMA reduces levels of serotonin (5-HT) 24 h after treatment on P11, however, learning deficits are seen after 5 or 10 days of drug treatment, not just 1 day. Accordingly, in the present experiment, rats were treated with MA or MDMA starting on P11 for 5 or 10 days (P11-15 or P11-20) and tissues collected on P16, P21, or P30. Five-day MA administration dramatically increased CORT on P16, whereas MDMA did not. Both drugs decreased hippocampal 5-HT on P16 and P21, although MDMA produced larger reductions. Ten-day treatment with either drug increased dopamine utilization in the neostriatum on P21, whereas 5-day treatment had no effect. No CORT or brain 5-HT or dopamine changes were found with either drug on P30. Although the monoamine changes are transient, they may alter developing neural circuits sufficiently to permanently disrupt later learning and memory abilities.

摘要

新生大鼠经(±)-3,4-亚甲基二氧甲基苯丙胺(摇头丸)或(+)-甲基苯丙胺(甲基安非他明)处理后会出现持久的学习障碍(即在出生后第(P)11 - 15天或P11 - 20天接受处理之后)。尽管这两种药物都是取代苯丙胺,但它们各自产生独特的认知缺陷模式(即空间学习与路径整合学习以及缺陷的严重程度),这可能是早期神经化学变化不同的结果。我们之前表明,在P11处理后24小时,甲基安非他明和摇头丸会增加皮质酮(CORT),而摇头丸会降低血清素(5-HT)水平,然而,在药物处理5天或10天后才出现学习缺陷,而非仅1天。因此,在本实验中,大鼠从P11开始接受甲基安非他明或摇头丸处理5天或10天(P11 - 15或P11 - 20),并在P16、P21或P30收集组织。连续5天给予甲基安非他明会使P16时的CORT显著增加,而摇头丸则不会。两种药物在P16和P21时都会降低海马体中的5-HT,尽管摇头丸导致的降低幅度更大。两种药物连续10天处理会使P21时新纹状体中的多巴胺利用率增加,而连续5天处理则没有效果。在P30时,两种药物均未引起CORT、脑5-HT或多巴胺的变化。尽管单胺变化是短暂的,但它们可能足以改变发育中的神经回路,从而永久性地破坏后期的学习和记忆能力。

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