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短期给予兴奋剂药物抑制成年大鼠海马区细胞增殖。

Suppression of hippocampal cell proliferation by short-term stimulant drug administration in adult rats.

机构信息

Program in Neuroscience, Princeton University, Princeton, NJ 08544, USA.

出版信息

Eur J Neurosci. 2009 Jun;29(11):2157-65. doi: 10.1111/j.1460-9568.2009.06759.x. Epub 2009 Jun 1.

Abstract

Sleep loss is known to potently suppress adult hippocampal cell proliferation and neurogenesis. Whether sleep suppression following acute administration of stimulant drugs also decreases hippocampal cell proliferation is not known. The present study examined the effect of three mechanistically distinct stimulants (caffeine, methamphetamine and modafinil) on cell proliferation. To maximize sleep suppression, these drugs were administered to rats (three i.p. injections, once every 4 h) during their sleep period (i.e. 12-h light phase). At the end of the light phase, 5-bromo-2'-deoxyuridine (200 mg/kg, i.p.) was injected and animals were killed 2 h later. Polygraphic recordings and locomotor activity measurements confirmed the wake-promoting and sleep-suppressing actions of each treatment. Results indicate that caffeine (20 mg/kg), methamphetamine (1.5 mg/kg) and modafinil (300 mg/kg) differentially suppressed sleep (45-91%) and selectively reduced cell proliferation in the hilus (12-44%), these results being significant for both caffeine and modafinil. When the same experiment was repeated in the dark (active) phase, the suppressant effect on hippocampal cell proliferation was either absent or greatly attenuated. In a further experiment, the effect of acute modafinil treatment in the light phase was shown to persist for 3 weeks after BrdU administration. We hypothesize that the differential effect of the stimulant drugs in the light vs. dark phase is attributable primarily to sleep suppression in the light. As abuse of stimulant drugs invariably leads to disrupted sleep in humans, our results suggest that they may, at least in part, decrease hippocampal neurogenesis via sleep loss and thereby adversely affect hippocampal-dependent processes.

摘要

睡眠缺失已知会强烈抑制成年海马体中的细胞增殖和神经发生。急性给予兴奋剂药物后是否会抑制睡眠从而减少海马体中的细胞增殖尚不清楚。本研究检测了三种作用机制不同的兴奋剂(咖啡因、甲基苯丙胺和莫达非尼)对细胞增殖的影响。为了最大程度地抑制睡眠,这些药物在大鼠的睡眠期(即 12 小时光照期)内通过腹腔注射(每 4 小时一次,共三次)给予大鼠。在光照期结束时,腹腔内注射 5-溴-2'-脱氧尿苷(200mg/kg),2 小时后处死动物。多导睡眠描记和运动活动测量证实了每种处理方法的促醒和睡眠抑制作用。结果表明,咖啡因(20mg/kg)、甲基苯丙胺(1.5mg/kg)和莫达非尼(300mg/kg)分别不同程度地抑制了睡眠(45-91%),并选择性地减少了齿状回(DG)中的细胞增殖(12-44%),这些结果对咖啡因和莫达非尼均有显著意义。当在黑暗(活跃)期重复进行相同的实验时,对海马体细胞增殖的抑制作用要么不存在,要么大大减弱。在进一步的实验中,显示在光照期急性给予莫达非尼治疗的效果在 BrdU 给药后持续了 3 周。我们假设,兴奋剂药物在光照期与黑暗期的不同作用主要归因于光照期的睡眠抑制。由于滥用兴奋剂药物在人类中不可避免地导致睡眠中断,我们的结果表明,它们可能至少部分地通过睡眠缺失而减少海马体神经发生,并因此对海马体依赖的过程产生不利影响。

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